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Friday 25 October 2013

Interview from Cancer Network by Dr.Kelly K. Hunt:Sentinel Lymph Node Surgery for Breast Cancer

A recent prospective trial showed sentinel lymph node surgery has a clinically significant high false
negative rate in breast cancer patients with node-positive disease receiving neoadjuvant
chemotherapy. In this interview we discuss surgical techniques that detect breast cancer in lymph
nodes.
Source:
Today we are discussing surgical techniques that detect breast cancer in lymph nodes, with Dr. Kelly
K. Hunt, professor in the department of surgical oncology at the University of Texas MD Anderson
Cancer Center in Houston. Dr. Hunt was part of a recent prospective trial that showed sentinel lymph
node surgery has a clinically significant high false negative rate in breast cancer patients with
node-positive disease, who are receiving neoadjuvant chemotherapy.
—Interviewed by Anna Azvolinsky, PhD
Cancer Network: Dr. Hunt, can you first describe the different surgery approaches currently used to detect
cancer in lymph nodes for breast cancer patients?

Dr. Hunt: The standard approach for many, many years has been to perform an axillary lymph node
dissection, where all of the lymph nodes are removed in the armpit area, and these are level 1 and 2
lymph nodes anatomically. For decades that has been used to, first of all, identify lymph nodes in the
area, and second, submit them for pathological processing to determine if there is any metastasis.
When sentinel lymph node surgery was developed in the 1990s, it was a method of identifying the
lymph nodes that are directly connected to the primary tumor through lymphatic channels, so that
those first important lymph nodes, the sentinel lymph nodes, can be removed to assess for any
metastasis. This can replace the need to remove all of the lymph nodes in women who actually don’t
have any disease in the lymph nodes.
Another tool that we use is ultrasound. This is something that has evolved over the last 10 to 20
years. Breast imaging specialists have been the main individuals using ultrasound to not only look at
the tumor in the breast, but also at the lymph nodes, and by looking at anatomical variables, they
know the normal architecture of the nodes. If they see changes in the anatomy and architecture of
the nodes, that can be a sign that the cancer has spread to the nodes, and they can use fine-needle
aspiration biopsy or core needle biopsy to sample that lymph node. So, that is a newer technique,
and surgeons have also been gaining experience with that technique in addition to breast imaging
specialists.
Cancer Network: What are the strengths and weaknesses of each of these surgical procedures? Do some
patients receive one technique over another?

Dr. Hunt: The reason why sentinel lymph node surgery was developed was because we had improvement
in screening, and with a lot more public awareness, cancers are detected earlier, when they are
developing within the breast, so there is less likelihood that they will have spread to the regional
nodes. Doing an axillary lymph node dissection for staging has really fallen out of favor because it is
associated particularly with lymphedema. Lymphedema is when there is swelling in the arm that can
progress from what looks like just a small amount of increase in the circumference of the arm to a
very large, swollen extremity that is more susceptible to infection, and it is very challenging to treat
for some women and is not a reversible condition. So, because we know that between 20% to 60% of
women will develop lymphedema with axillary lymph node dissection, depending on how
measurements are made and how frequently the patients are seen in follow-up, we want to avoid
that at all costs. That is a really difficult thing for patients to recover from.
The sentinel lymph node surgery as a replacement for axillary lymph node dissection is associated  with a much lower risk of lymphedema. Lymphedema is the one patients worry about the most, but
there are other complications that occur, including seroma formation, which is the collection of fluid
in the armpit area after axillary lymph node dissection, or infections due to the fluid that has
developed there. Or patients develop problems with range of motion when they are trying to move
the upper extremity and shoulder, because scar tissue that develops in the armpit area after the
axillary nodes are removed can result in a lot of tightening of the tissue and scarring, which can limit
the range of motion in the shoulder.
Finally, there are nerves that go through the axillary lymph node area that supply sensation to the
upper arm, especially the back of the upper arm area, and so, in doing lymph node dissection those
nerves are often disrupted, and women often have numbness or abnormal sensations of pain in the
upper arm because of that lymph node surgery. There are a number of reasons why we would not
want to do axillary lymph node dissection if we don’t need to because of the potential complications
that women have to live with afterwards. But, of course, we want to be certain that we accurately
stage the disease, and that we do remove any cancer that may be a source of future problems in
terms of metastatic disease in other organs. So, there is definitely a balance between doing the
surgery and making sure that we are accurately assessing the stage and disease process, but we do
want to limit the amount of side effects for the patients.
Cancer Network: In the study that you and colleagues published recently, you find that the false negative rate
of sentinel lymph node surgery is relatively high in patients who have node-positive breast cancer
who had neoadjuvant chemotherapy. Can you describe this trial?

Dr. Hunt: The reason we were interested in doing this trial is because, as I said, sometimes we use
ultrasound to assess women when they’re first diagnosed with breast cancer, and we identify lymph
nodes in the axillary that look abnormal. We do a biopsy to prove that they are abnormal, and that
can be an indication to do chemotherapy before any surgical intervention. What we found over the
past 10 years of using chemotherapy before surgery is that about 40% of the time, women who had
evidence of lymph node involvement based on the biopsy will no longer have any disease in the
lymph nodes at surgery, because the chemotherapy can eradicate the disease not only in the breast
but also in the lymph nodes and other parts of the body. Now that this neoadjuvant chemotherapy
has become more common in women with earlier-stage breast cancer, and we find that we are
eradicating the disease more frequently, we wanted to see if we can use a less invasive approach
after chemotherapy to see if we had eradicated the disease in the lymph nodes, and therefore, didn’t
need to do a full axillary lymph node dissection.
This trial was designed to have women who had evidence of disease in the lymph nodes confirmed
by needle biopsy receive chemotherapy. After chemotherapy, they were scheduled to have sentinel
lymph node surgery at the same time as the axillary lymph node dissection, and then pathologists
would assess how accurate the sentinel lymph node surgery was in determining the status of those
lymph nodes. So, what we found was that 91% of the time the sentinel lymph node did reflect the
status of the axilla. In women where the sentinel node was negative, the axilla was negative, and
when the sentinel node was positive, the axillary lymph nodes were positive; it was accurate. But we
know that in some women, the sentinel node was negative for any cancer, but there were axillary
lymph nodes that had disease in them, meaning that was a false negative result, and that the
sentinel node did not accurately stage the axilla.
The concern there, of course, is that you are leaving disease behind, if you did only the sentinel node
surgery and the sentinel node was negative. This has always been a concern since this technique
was developed—we knew that there was a chance of a false negative event. Several prospective
trials have shown that if you pay attention to how the sentinel lymph node surgery is performed, you
can reduce the chance that there will be a false negative result. That is why we had recommended
that surgeons use both blue dye and radiolabeled colloid to perform the sentinel lymph node
surgery, because we knew that reduces the false negative rate. We also knew that if you remove
more than two sentinel nodes, it reduces the false negative rate. The reason for that is that most
women do have more than one sentinel node. There are usually two or three, and most studies have
shown that there are two or three, because the lymphatic drainage of the breast is quite complex.
What we had recommended is that surgeons remove at least two sentinel nodes, not that they should randomly take additional nodes, but that they should really try to be very complete in the
sentinel lymph node surgery before they went on to do the axillary lymph node dissection. Previous
studies have shown that when surgeons are doing the sentinel node surgery at the same time as the
axillary node dissection, oftentimes if they identify one central node, they will stop and then do the
axillary node dissection, but we know that that will cause false negative events because the central
node they recover may not have been the one that had metastatic disease at presentation, and they
still may have disease on axillary lymph node dissection.
So, what we found is that the false negative rate was higher than what we had set as our predefined
rate that we would accept, being 10%. We found a rate of 12.6%, but if we look at when the
techniques were employed that we had recommended, namely dual agents for the mapping, and
more than two sentinel nodes recovered, then the false negative rate falls below that preset
endpoint.
Cancer Network: What are the implications of this study?
Dr. Hunt: I think the implications are that if the attention to the surgical procedure is carefully discerned
by the surgeon, then we can use this technique for staging the axilla after chemotherapy. But the
other thing that we found from this trial is that we need to select the patients very carefully. Just as
we would select a patient for using chemotherapy or not, or using hormonal therapy or not, to treat
their cancer, we need to select patients very carefully for this type of surgery as well. In other words,
we would want to see that the patient had not only had the chemotherapy, but that the lymph nodes
that were detected at that initial presentation do show evidence of response based on ultrasound
and physical examination, whereas in the trial we are discussing, the patients were just selected
based on having a lymph node that was identified at presentation, and then they had chemotherapy
and surgery, and we did not exclude them if they still had evidence of disease based on ultrasound
or other imaging techniques. The implications are that we can be less invasive with our surgical
approaches, but we have to be careful in how we select our patients and how we perform the
procedure, and that we are certain that we remove all of the sentinel nodes to be sure we are
getting an accurate staging.
Cancer Network: Are there any studies that are following up on these results that you can highlight?
Dr. Hunt: There have been a couple recent studies showing that in women who present initially for breast
surgery and have sentinel lymph node surgery and there is a positive sentinel node, if they are
randomized to undergo axillary dissection versus axillary radiation, the axillary radiation appears to
control any residual disease that might be there just as well as doing an axillary dissection. And it
seems to have a lower rate of side effects, mainly lymphedema. One trial that we have that is now
open, recently activated through the alliance for clinical trials in oncology, is a study in which we are
assessing patients who present with node-positive disease, have chemotherapy, and then if after
chemotherapy they had a good response in the lymph nodes, but we do a sentinel node biopsy and
it still shows disease in the sentinel node, we are randomizing them to have axillary dissection
versus radiation, because we think the radiation may have fewer side effects and will still be a good
option for controlling any residual disease that might still be there.
Cancer Network: Thank you so much for joining us today, Dr. Hunt.
Dr. Hunt: Thank you.
Source URL: http://www.cancernetwork.com/articles/sentinel-lymph-node-surgery-breast-cancer
Links:
[1] http://www.cancernetwork.com/authors/kelly-k-hunt-md
Today we are discussing surgical techniques that detect breast cancer in lymph nodes, with Dr. Kelly K. Hunt, professor in the department of surgical oncology at the University of Texas MD Anderson Cancer Center in Houston. Dr. Hunt was part of a recent prospective trial that showed sentinel lymph node surgery has a clinically significant high false negative rate in breast cancer patients with node-positive disease, who are receiving neoadjuvant chemotherapy.
—Interviewed by Anna Azvolinsky, PhD
Cancer Network: Dr. Hunt, can you first describe the different surgery approaches currently used to detect cancer in lymph nodes for breast cancer patients?
Dr. Hunt: The standard approach for many, many years has been to perform an axillary lymph node dissection, where all of the lymph nodes are removed in the armpit area, and these are level 1 and 2 lymph nodes anatomically. For decades that has been used to, first of all, identify lymph nodes in the area, and second, submit them for pathological processing to determine if there is any metastasis. When sentinel lymph node surgery was developed in the 1990s, it was a method of identifying the lymph nodes that are directly connected to the primary tumor through lymphatic channels, so that those first important lymph nodes, the sentinel lymph nodes, can be removed to assess for any metastasis. This can replace the need to remove all of the lymph nodes in women who actually don’t have any disease in the lymph nodes.
Another tool that we use is ultrasound. This is something that has evolved over the last 10 to 20 years. Breast imaging specialists have been the main individuals using ultrasound to not only look at the tumor in the breast, but also at the lymph nodes, and by looking at anatomical variables, they know the normal architecture of the nodes. If they see changes in the anatomy and architecture of the nodes, that can be a sign that the cancer has spread to the nodes, and they can use fine-needle aspiration biopsy or core needle biopsy to sample that lymph node. So, that is a newer technique, and surgeons have also been gaining experience with that technique in addition to breast imaging specialists.
Cancer Network: What are the strengths and weaknesses of each of these surgical procedures? Do some patients receive one technique over another?
Dr. Hunt: The reason why sentinel lymph node surgery was developed was because we had improvement in screening, and with a lot more public awareness, cancers are detected earlier, when they are developing within the breast, so there is less likelihood that they will have spread to the regional nodes. Doing an axillary lymph node dissection for staging has really fallen out of favor because it is associated particularly with lymphedema. Lymphedema is when there is swelling in the arm that can progress from what looks like just a small amount of increase in the circumference of the arm to a very large, swollen extremity that is more susceptible to infection, and it is very challenging to treat for some women and is not a reversible condition. So, because we know that between 20% to 60% of women will develop lymphedema with axillary lymph node dissection, depending on how measurements are made and how frequently the patients are seen in follow-up, we want to avoid that at all costs. That is a really difficult thing for patients to recover from.
The sentinel lymph node surgery as a replacement for axillary lymph node dissection is associated with a much lower risk of lymphedema. Lymphedema is the one patients worry about the most, but there are other complications that occur, including seroma formation, which is the collection of fluid in the armpit area after axillary lymph node dissection, or infections due to the fluid that has developed there. Or patients develop problems with range of motion when they are trying to move the upper extremity and shoulder, because scar tissue that develops in the armpit area after the axillary nodes are removed can result in a lot of tightening of the tissue and scarring, which can limit the range of motion in the shoulder.
Finally, there are nerves that go through the axillary lymph node area that supply sensation to the upper arm, especially the back of the upper arm area, and so, in doing lymph node dissection those nerves are often disrupted, and women often have numbness or abnormal sensations of pain in the upper arm because of that lymph node surgery. There are a number of reasons why we would not want to do axillary lymph node dissection if we don’t need to because of the potential complications that women have to live with afterwards. But, of course, we want to be certain that we accurately stage the disease, and that we do remove any cancer that may be a source of future problems in terms of metastatic disease in other organs. So, there is definitely a balance between doing the surgery and making sure that we are accurately assessing the stage and disease process, but we do want to limit the amount of side effects for the patients.
Cancer Network: In the study that you and colleagues published recently, you find that the false negative rate of sentinel lymph node surgery is relatively high in patients who have node-positive breast cancer who had neoadjuvant chemotherapy. Can you describe this trial?
Dr. Hunt: The reason we were interested in doing this trial is because, as I said, sometimes we use ultrasound to assess women when they’re first diagnosed with breast cancer, and we identify lymph nodes in the axillary that look abnormal. We do a biopsy to prove that they are abnormal, and that can be an indication to do chemotherapy before any surgical intervention. What we found over the past 10 years of using chemotherapy before surgery is that about 40% of the time, women who had evidence of lymph node involvement based on the biopsy will no longer have any disease in the lymph nodes at surgery, because the chemotherapy can eradicate the disease not only in the breast but also in the lymph nodes and other parts of the body. Now that this neoadjuvant chemotherapy has become more common in women with earlier-stage breast cancer, and we find that we are eradicating the disease more frequently, we wanted to see if we can use a less invasive approach after chemotherapy to see if we had eradicated the disease in the lymph nodes, and therefore, didn’t need to do a full axillary lymph node dissection.
This trial was designed to have women who had evidence of disease in the lymph nodes confirmed by needle biopsy receive chemotherapy. After chemotherapy, they were scheduled to have sentinel lymph node surgery at the same time as the axillary lymph node dissection, and then pathologists would assess how accurate the sentinel lymph node surgery was in determining the status of those lymph nodes. So, what we found was that 91% of the time the sentinel lymph node did reflect the status of the axilla. In women where the sentinel node was negative, the axilla was negative, and when the sentinel node was positive, the axillary lymph nodes were positive; it was accurate. But we know that in some women, the sentinel node was negative for any cancer, but there were axillary lymph nodes that had disease in them, meaning that was a false negative result, and that the sentinel node did not accurately stage the axilla.
The concern there, of course, is that you are leaving disease behind, if you did only the sentinel node surgery and the sentinel node was negative. This has always been a concern since this technique was developed—we knew that there was a chance of a false negative event. Several prospective trials have shown that if you pay attention to how the sentinel lymph node surgery is performed, you can reduce the chance that there will be a false negative result. That is why we had recommended that surgeons use both blue dye and radiolabeled colloid to perform the sentinel lymph node surgery, because we knew that reduces the false negative rate. We also knew that if you remove more than two sentinel nodes, it reduces the false negative rate. The reason for that is that most women do have more than one sentinel node. There are usually two or three, and most studies have shown that there are two or three, because the lymphatic drainage of the breast is quite complex. What we had recommended is that surgeons remove at least two sentinel nodes, not that they should randomly take additional nodes, but that they should really try to be very complete in the sentinel lymph node surgery before they went on to do the axillary lymph node dissection. Previous studies have shown that when surgeons are doing the sentinel node surgery at the same time as the axillary node dissection, oftentimes if they identify one central node, they will stop and then do the axillary node dissection, but we know that that will cause false negative events because the central node they recover may not have been the one that had metastatic disease at presentation, and they still may have disease on axillary lymph node dissection.
So, what we found is that the false negative rate was higher than what we had set as our predefined rate that we would accept, being 10%. We found a rate of 12.6%, but if we look at when the techniques were employed that we had recommended, namely dual agents for the mapping, and more than two sentinel nodes recovered, then the false negative rate falls below that preset endpoint.
Cancer Network: What are the implications of this study?
Dr. Hunt: I think the implications are that if the attention to the surgical procedure is carefully discerned by the surgeon, then we can use this technique for staging the axilla after chemotherapy. But the other thing that we found from this trial is that we need to select the patients very carefully. Just as we would select a patient for using chemotherapy or not, or using hormonal therapy or not, to treat their cancer, we need to select patients very carefully for this type of surgery as well. In other words, we would want to see that the patient had not only had the chemotherapy, but that the lymph nodes that were detected at that initial presentation do show evidence of response based on ultrasound and physical examination, whereas in the trial we are discussing, the patients were just selected based on having a lymph node that was identified at presentation, and then they had chemotherapy and surgery, and we did not exclude them if they still had evidence of disease based on ultrasound or other imaging techniques. The implications are that we can be less invasive with our surgical approaches, but we have to be careful in how we select our patients and how we perform the procedure, and that we are certain that we remove all of the sentinel nodes to be sure we are getting an accurate staging.
Cancer Network: Are there any studies that are following up on these results that you can highlight?
Dr. Hunt: There have been a couple recent studies showing that in women who present initially for breast surgery and have sentinel lymph node surgery and there is a positive sentinel node, if they are randomized to undergo axillary dissection versus axillary radiation, the axillary radiation appears to control any residual disease that might be there just as well as doing an axillary dissection. And it seems to have a lower rate of side effects, mainly lymphedema. One trial that we have that is now open, recently activated through the alliance for clinical trials in oncology, is a study in which we are assessing patients who present with node-positive disease, have chemotherapy, and then if after chemotherapy they had a good response in the lymph nodes, but we do a sentinel node biopsy and it still shows disease in the sentinel node, we are randomizing them to have axillary dissection versus radiation, because we think the radiation may have fewer side effects and will still be a good option for controlling any residual disease that might still be there.
Cancer Network: Thank you so much for joining us today, Dr. Hunt.
Dr. Hunt: Thank you.
- See more at: http://www.cancernetwork.com/podcasts/sentinel-lymph-node-surgery-breast-cancer?GUID=493C0B05-172C-4898-9E4B-DE045D6D2BF5&rememberme=1&ts=25102013#sthash.7lP63C47.dpuf
Cancer Network: Dr. Hunt, can you first describe the different surgery approaches currently used to detect cancer in lymph nodes for breast cancer patients?
Dr. Hunt: The standard approach for many, many years has been to perform an axillary lymph node dissection, where all of the lymph nodes are removed in the armpit area, and these are level 1 and 2 lymph nodes anatomically. For decades that has been used to, first of all, identify lymph nodes in the area, and second, submit them for pathological processing to determine if there is any metastasis. When sentinel lymph node surgery was developed in the 1990s, it was a method of identifying the lymph nodes that are directly connected to the primary tumor through lymphatic channels, so that those first important lymph nodes, the sentinel lymph nodes, can be removed to assess for any metastasis. This can replace the need to remove all of the lymph nodes in women who actually don’t have any disease in the lymph nodes.
Another tool that we use is ultrasound. This is something that has evolved over the last 10 to 20 years. Breast imaging specialists have been the main individuals using ultrasound to not only look at the tumor in the breast, but also at the lymph nodes, and by looking at anatomical variables, they know the normal architecture of the nodes. If they see changes in the anatomy and architecture of the nodes, that can be a sign that the cancer has spread to the nodes, and they can use fine-needle aspiration biopsy or core needle biopsy to sample that lymph node. So, that is a newer technique, and surgeons have also been gaining experience with that technique in addition to breast imaging specialists.
Cancer Network: What are the strengths and weaknesses of each of these surgical procedures? Do some patients receive one technique over another?
Dr. Hunt: The reason why sentinel lymph node surgery was developed was because we had improvement in screening, and with a lot more public awareness, cancers are detected earlier, when they are developing within the breast, so there is less likelihood that they will have spread to the regional nodes. Doing an axillary lymph node dissection for staging has really fallen out of favor because it is associated particularly with lymphedema. Lymphedema is when there is swelling in the arm that can progress from what looks like just a small amount of increase in the circumference of the arm to a very large, swollen extremity that is more susceptible to infection, and it is very challenging to treat for some women and is not a reversible condition. So, because we know that between 20% to 60% of women will develop lymphedema with axillary lymph node dissection, depending on how measurements are made and how frequently the patients are seen in follow-up, we want to avoid that at all costs. That is a really difficult thing for patients to recover from.
The sentinel lymph node surgery as a replacement for axillary lymph node dissection is associated with a much lower risk of lymphedema. Lymphedema is the one patients worry about the most, but there are other complications that occur, including seroma formation, which is the collection of fluid in the armpit area after axillary lymph node dissection, or infections due to the fluid that has developed there. Or patients develop problems with range of motion when they are trying to move the upper extremity and shoulder, because scar tissue that develops in the armpit area after the axillary nodes are removed can result in a lot of tightening of the tissue and scarring, which can limit the range of motion in the shoulder.
Finally, there are nerves that go through the axillary lymph node area that supply sensation to the upper arm, especially the back of the upper arm area, and so, in doing lymph node dissection those nerves are often disrupted, and women often have numbness or abnormal sensations of pain in the upper arm because of that lymph node surgery. There are a number of reasons why we would not want to do axillary lymph node dissection if we don’t need to because of the potential complications that women have to live with afterwards. But, of course, we want to be certain that we accurately stage the disease, and that we do remove any cancer that may be a source of future problems in terms of metastatic disease in other organs. So, there is definitely a balance between doing the surgery and making sure that we are accurately assessing the stage and disease process, but we do want to limit the amount of side effects for the patients.
Cancer Network: In the study that you and colleagues published recently, you find that the false negative rate of sentinel lymph node surgery is relatively high in patients who have node-positive breast cancer who had neoadjuvant chemotherapy. Can you describe this trial?
Dr. Hunt: The reason we were interested in doing this trial is because, as I said, sometimes we use ultrasound to assess women when they’re first diagnosed with breast cancer, and we identify lymph nodes in the axillary that look abnormal. We do a biopsy to prove that they are abnormal, and that can be an indication to do chemotherapy before any surgical intervention. What we found over the past 10 years of using chemotherapy before surgery is that about 40% of the time, women who had evidence of lymph node involvement based on the biopsy will no longer have any disease in the lymph nodes at surgery, because the chemotherapy can eradicate the disease not only in the breast but also in the lymph nodes and other parts of the body. Now that this neoadjuvant chemotherapy has become more common in women with earlier-stage breast cancer, and we find that we are eradicating the disease more frequently, we wanted to see if we can use a less invasive approach after chemotherapy to see if we had eradicated the disease in the lymph nodes, and therefore, didn’t need to do a full axillary lymph node dissection.
This trial was designed to have women who had evidence of disease in the lymph nodes confirmed by needle biopsy receive chemotherapy. After chemotherapy, they were scheduled to have sentinel lymph node surgery at the same time as the axillary lymph node dissection, and then pathologists would assess how accurate the sentinel lymph node surgery was in determining the status of those lymph nodes. So, what we found was that 91% of the time the sentinel lymph node did reflect the status of the axilla. In women where the sentinel node was negative, the axilla was negative, and when the sentinel node was positive, the axillary lymph nodes were positive; it was accurate. But we know that in some women, the sentinel node was negative for any cancer, but there were axillary lymph nodes that had disease in them, meaning that was a false negative result, and that the sentinel node did not accurately stage the axilla.
The concern there, of course, is that you are leaving disease behind, if you did only the sentinel node surgery and the sentinel node was negative. This has always been a concern since this technique was developed—we knew that there was a chance of a false negative event. Several prospective trials have shown that if you pay attention to how the sentinel lymph node surgery is performed, you can reduce the chance that there will be a false negative result. That is why we had recommended that surgeons use both blue dye and radiolabeled colloid to perform the sentinel lymph node surgery, because we knew that reduces the false negative rate. We also knew that if you remove more than two sentinel nodes, it reduces the false negative rate. The reason for that is that most women do have more than one sentinel node. There are usually two or three, and most studies have shown that there are two or three, because the lymphatic drainage of the breast is quite complex. What we had recommended is that surgeons remove at least two sentinel nodes, not that they should randomly take additional nodes, but that they should really try to be very complete in the sentinel lymph node surgery before they went on to do the axillary lymph node dissection. Previous studies have shown that when surgeons are doing the sentinel node surgery at the same time as the axillary node dissection, oftentimes if they identify one central node, they will stop and then do the axillary node dissection, but we know that that will cause false negative events because the central node they recover may not have been the one that had metastatic disease at presentation, and they still may have disease on axillary lymph node dissection.
So, what we found is that the false negative rate was higher than what we had set as our predefined rate that we would accept, being 10%. We found a rate of 12.6%, but if we look at when the techniques were employed that we had recommended, namely dual agents for the mapping, and more than two sentinel nodes recovered, then the false negative rate falls below that preset endpoint.
Cancer Network: What are the implications of this study?
Dr. Hunt: I think the implications are that if the attention to the surgical procedure is carefully discerned by the surgeon, then we can use this technique for staging the axilla after chemotherapy. But the other thing that we found from this trial is that we need to select the patients very carefully. Just as we would select a patient for using chemotherapy or not, or using hormonal therapy or not, to treat their cancer, we need to select patients very carefully for this type of surgery as well. In other words, we would want to see that the patient had not only had the chemotherapy, but that the lymph nodes that were detected at that initial presentation do show evidence of response based on ultrasound and physical examination, whereas in the trial we are discussing, the patients were just selected based on having a lymph node that was identified at presentation, and then they had chemotherapy and surgery, and we did not exclude them if they still had evidence of disease based on ultrasound or other imaging techniques. The implications are that we can be less invasive with our surgical approaches, but we have to be careful in how we select our patients and how we perform the procedure, and that we are certain that we remove all of the sentinel nodes to be sure we are getting an accurate staging.
Cancer Network: Are there any studies that are following up on these results that you can highlight?
Dr. Hunt: There have been a couple recent studies showing that in women who present initially for breast surgery and have sentinel lymph node surgery and there is a positive sentinel node, if they are randomized to undergo axillary dissection versus axillary radiation, the axillary radiation appears to control any residual disease that might be there just as well as doing an axillary dissection. And it seems to have a lower rate of side effects, mainly lymphedema. One trial that we have that is now open, recently activated through the alliance for clinical trials in oncology, is a study in which we are assessing patients who present with node-positive disease, have chemotherapy, and then if after chemotherapy they had a good response in the lymph nodes, but we do a sentinel node biopsy and it still shows disease in the sentinel node, we are randomizing them to have axillary dissection versus radiation, because we think the radiation may have fewer side effects and will still be a good option for controlling any residual disease that might still be there.
Cancer Network: Thank you so much for joining us today, Dr. Hunt.
Dr. Hunt: Thank you.
- See more at: http://www.cancernetwork.com/podcasts/sentinel-lymph-node-surgery-breast-cancer?GUID=493C0B05-172C-4898-9E4B-DE045D6D2BF5&rememberme=1&ts=25102013#sthash.Wq91TFah.dpuf
Cancer Network: Dr. Hunt, can you first describe the different surgery approaches currently used to detect cancer in lymph nodes for breast cancer patients?
Dr. Hunt: The standard approach for many, many years has been to perform an axillary lymph node dissection, where all of the lymph nodes are removed in the armpit area, and these are level 1 and 2 lymph nodes anatomically. For decades that has been used to, first of all, identify lymph nodes in the area, and second, submit them for pathological processing to determine if there is any metastasis. When sentinel lymph node surgery was developed in the 1990s, it was a method of identifying the lymph nodes that are directly connected to the primary tumor through lymphatic channels, so that those first important lymph nodes, the sentinel lymph nodes, can be removed to assess for any metastasis. This can replace the need to remove all of the lymph nodes in women who actually don’t have any disease in the lymph nodes.
Another tool that we use is ultrasound. This is something that has evolved over the last 10 to 20 years. Breast imaging specialists have been the main individuals using ultrasound to not only look at the tumor in the breast, but also at the lymph nodes, and by looking at anatomical variables, they know the normal architecture of the nodes. If they see changes in the anatomy and architecture of the nodes, that can be a sign that the cancer has spread to the nodes, and they can use fine-needle aspiration biopsy or core needle biopsy to sample that lymph node. So, that is a newer technique, and surgeons have also been gaining experience with that technique in addition to breast imaging specialists.
Cancer Network: What are the strengths and weaknesses of each of these surgical procedures? Do some patients receive one technique over another?
Dr. Hunt: The reason why sentinel lymph node surgery was developed was because we had improvement in screening, and with a lot more public awareness, cancers are detected earlier, when they are developing within the breast, so there is less likelihood that they will have spread to the regional nodes. Doing an axillary lymph node dissection for staging has really fallen out of favor because it is associated particularly with lymphedema. Lymphedema is when there is swelling in the arm that can progress from what looks like just a small amount of increase in the circumference of the arm to a very large, swollen extremity that is more susceptible to infection, and it is very challenging to treat for some women and is not a reversible condition. So, because we know that between 20% to 60% of women will develop lymphedema with axillary lymph node dissection, depending on how measurements are made and how frequently the patients are seen in follow-up, we want to avoid that at all costs. That is a really difficult thing for patients to recover from.
The sentinel lymph node surgery as a replacement for axillary lymph node dissection is associated with a much lower risk of lymphedema. Lymphedema is the one patients worry about the most, but there are other complications that occur, including seroma formation, which is the collection of fluid in the armpit area after axillary lymph node dissection, or infections due to the fluid that has developed there. Or patients develop problems with range of motion when they are trying to move the upper extremity and shoulder, because scar tissue that develops in the armpit area after the axillary nodes are removed can result in a lot of tightening of the tissue and scarring, which can limit the range of motion in the shoulder.
Finally, there are nerves that go through the axillary lymph node area that supply sensation to the upper arm, especially the back of the upper arm area, and so, in doing lymph node dissection those nerves are often disrupted, and women often have numbness or abnormal sensations of pain in the upper arm because of that lymph node surgery. There are a number of reasons why we would not want to do axillary lymph node dissection if we don’t need to because of the potential complications that women have to live with afterwards. But, of course, we want to be certain that we accurately stage the disease, and that we do remove any cancer that may be a source of future problems in terms of metastatic disease in other organs. So, there is definitely a balance between doing the surgery and making sure that we are accurately assessing the stage and disease process, but we do want to limit the amount of side effects for the patients.
Cancer Network: In the study that you and colleagues published recently, you find that the false negative rate of sentinel lymph node surgery is relatively high in patients who have node-positive breast cancer who had neoadjuvant chemotherapy. Can you describe this trial?
Dr. Hunt: The reason we were interested in doing this trial is because, as I said, sometimes we use ultrasound to assess women when they’re first diagnosed with breast cancer, and we identify lymph nodes in the axillary that look abnormal. We do a biopsy to prove that they are abnormal, and that can be an indication to do chemotherapy before any surgical intervention. What we found over the past 10 years of using chemotherapy before surgery is that about 40% of the time, women who had evidence of lymph node involvement based on the biopsy will no longer have any disease in the lymph nodes at surgery, because the chemotherapy can eradicate the disease not only in the breast but also in the lymph nodes and other parts of the body. Now that this neoadjuvant chemotherapy has become more common in women with earlier-stage breast cancer, and we find that we are eradicating the disease more frequently, we wanted to see if we can use a less invasive approach after chemotherapy to see if we had eradicated the disease in the lymph nodes, and therefore, didn’t need to do a full axillary lymph node dissection.
This trial was designed to have women who had evidence of disease in the lymph nodes confirmed by needle biopsy receive chemotherapy. After chemotherapy, they were scheduled to have sentinel lymph node surgery at the same time as the axillary lymph node dissection, and then pathologists would assess how accurate the sentinel lymph node surgery was in determining the status of those lymph nodes. So, what we found was that 91% of the time the sentinel lymph node did reflect the status of the axilla. In women where the sentinel node was negative, the axilla was negative, and when the sentinel node was positive, the axillary lymph nodes were positive; it was accurate. But we know that in some women, the sentinel node was negative for any cancer, but there were axillary lymph nodes that had disease in them, meaning that was a false negative result, and that the sentinel node did not accurately stage the axilla.
The concern there, of course, is that you are leaving disease behind, if you did only the sentinel node surgery and the sentinel node was negative. This has always been a concern since this technique was developed—we knew that there was a chance of a false negative event. Several prospective trials have shown that if you pay attention to how the sentinel lymph node surgery is performed, you can reduce the chance that there will be a false negative result. That is why we had recommended that surgeons use both blue dye and radiolabeled colloid to perform the sentinel lymph node surgery, because we knew that reduces the false negative rate. We also knew that if you remove more than two sentinel nodes, it reduces the false negative rate. The reason for that is that most women do have more than one sentinel node. There are usually two or three, and most studies have shown that there are two or three, because the lymphatic drainage of the breast is quite complex. What we had recommended is that surgeons remove at least two sentinel nodes, not that they should randomly take additional nodes, but that they should really try to be very complete in the sentinel lymph node surgery before they went on to do the axillary lymph node dissection. Previous studies have shown that when surgeons are doing the sentinel node surgery at the same time as the axillary node dissection, oftentimes if they identify one central node, they will stop and then do the axillary node dissection, but we know that that will cause false negative events because the central node they recover may not have been the one that had metastatic disease at presentation, and they still may have disease on axillary lymph node dissection.
So, what we found is that the false negative rate was higher than what we had set as our predefined rate that we would accept, being 10%. We found a rate of 12.6%, but if we look at when the techniques were employed that we had recommended, namely dual agents for the mapping, and more than two sentinel nodes recovered, then the false negative rate falls below that preset endpoint.
Cancer Network: What are the implications of this study?
Dr. Hunt: I think the implications are that if the attention to the surgical procedure is carefully discerned by the surgeon, then we can use this technique for staging the axilla after chemotherapy. But the other thing that we found from this trial is that we need to select the patients very carefully. Just as we would select a patient for using chemotherapy or not, or using hormonal therapy or not, to treat their cancer, we need to select patients very carefully for this type of surgery as well. In other words, we would want to see that the patient had not only had the chemotherapy, but that the lymph nodes that were detected at that initial presentation do show evidence of response based on ultrasound and physical examination, whereas in the trial we are discussing, the patients were just selected based on having a lymph node that was identified at presentation, and then they had chemotherapy and surgery, and we did not exclude them if they still had evidence of disease based on ultrasound or other imaging techniques. The implications are that we can be less invasive with our surgical approaches, but we have to be careful in how we select our patients and how we perform the procedure, and that we are certain that we remove all of the sentinel nodes to be sure we are getting an accurate staging.
Cancer Network: Are there any studies that are following up on these results that you can highlight?
Dr. Hunt: There have been a couple recent studies showing that in women who present initially for breast surgery and have sentinel lymph node surgery and there is a positive sentinel node, if they are randomized to undergo axillary dissection versus axillary radiation, the axillary radiation appears to control any residual disease that might be there just as well as doing an axillary dissection. And it seems to have a lower rate of side effects, mainly lymphedema. One trial that we have that is now open, recently activated through the alliance for clinical trials in oncology, is a study in which we are assessing patients who present with node-positive disease, have chemotherapy, and then if after chemotherapy they had a good response in the lymph nodes, but we do a sentinel node biopsy and it still shows disease in the sentinel node, we are randomizing them to have axillary dissection versus radiation, because we think the radiation may have fewer side effects and will still be a good option for controlling any residual disease that might still be there.
Cancer Network: Thank you so much for joining us today, Dr. Hunt.
Dr. Hunt: Thank you.
- See more at: http://www.cancernetwork.com/podcasts/sentinel-lymph-node-surgery-breast-cancer?GUID=493C0B05-172C-4898-9E4B-DE045D6D2BF5&rememberme=1&ts=25102013#sthash.Wq91TFah.dpuf
Cancer Network: Dr. Hunt, can you first describe the different surgery approaches currently used to detect cancer in lymph nodes for breast cancer patients?
Dr. Hunt: The standard approach for many, many years has been to perform an axillary lymph node dissection, where all of the lymph nodes are removed in the armpit area, and these are level 1 and 2 lymph nodes anatomically. For decades that has been used to, first of all, identify lymph nodes in the area, and second, submit them for pathological processing to determine if there is any metastasis. When sentinel lymph node surgery was developed in the 1990s, it was a method of identifying the lymph nodes that are directly connected to the primary tumor through lymphatic channels, so that those first important lymph nodes, the sentinel lymph nodes, can be removed to assess for any metastasis. This can replace the need to remove all of the lymph nodes in women who actually don’t have any disease in the lymph nodes.
Another tool that we use is ultrasound. This is something that has evolved over the last 10 to 20 years. Breast imaging specialists have been the main individuals using ultrasound to not only look at the tumor in the breast, but also at the lymph nodes, and by looking at anatomical variables, they know the normal architecture of the nodes. If they see changes in the anatomy and architecture of the nodes, that can be a sign that the cancer has spread to the nodes, and they can use fine-needle aspiration biopsy or core needle biopsy to sample that lymph node. So, that is a newer technique, and surgeons have also been gaining experience with that technique in addition to breast imaging specialists.
Cancer Network: What are the strengths and weaknesses of each of these surgical procedures? Do some patients receive one technique over another?
Dr. Hunt: The reason why sentinel lymph node surgery was developed was because we had improvement in screening, and with a lot more public awareness, cancers are detected earlier, when they are developing within the breast, so there is less likelihood that they will have spread to the regional nodes. Doing an axillary lymph node dissection for staging has really fallen out of favor because it is associated particularly with lymphedema. Lymphedema is when there is swelling in the arm that can progress from what looks like just a small amount of increase in the circumference of the arm to a very large, swollen extremity that is more susceptible to infection, and it is very challenging to treat for some women and is not a reversible condition. So, because we know that between 20% to 60% of women will develop lymphedema with axillary lymph node dissection, depending on how measurements are made and how frequently the patients are seen in follow-up, we want to avoid that at all costs. That is a really difficult thing for patients to recover from.
The sentinel lymph node surgery as a replacement for axillary lymph node dissection is associated with a much lower risk of lymphedema. Lymphedema is the one patients worry about the most, but there are other complications that occur, including seroma formation, which is the collection of fluid in the armpit area after axillary lymph node dissection, or infections due to the fluid that has developed there. Or patients develop problems with range of motion when they are trying to move the upper extremity and shoulder, because scar tissue that develops in the armpit area after the axillary nodes are removed can result in a lot of tightening of the tissue and scarring, which can limit the range of motion in the shoulder.
Finally, there are nerves that go through the axillary lymph node area that supply sensation to the upper arm, especially the back of the upper arm area, and so, in doing lymph node dissection those nerves are often disrupted, and women often have numbness or abnormal sensations of pain in the upper arm because of that lymph node surgery. There are a number of reasons why we would not want to do axillary lymph node dissection if we don’t need to because of the potential complications that women have to live with afterwards. But, of course, we want to be certain that we accurately stage the disease, and that we do remove any cancer that may be a source of future problems in terms of metastatic disease in other organs. So, there is definitely a balance between doing the surgery and making sure that we are accurately assessing the stage and disease process, but we do want to limit the amount of side effects for the patients.
Cancer Network: In the study that you and colleagues published recently, you find that the false negative rate of sentinel lymph node surgery is relatively high in patients who have node-positive breast cancer who had neoadjuvant chemotherapy. Can you describe this trial?
Dr. Hunt: The reason we were interested in doing this trial is because, as I said, sometimes we use ultrasound to assess women when they’re first diagnosed with breast cancer, and we identify lymph nodes in the axillary that look abnormal. We do a biopsy to prove that they are abnormal, and that can be an indication to do chemotherapy before any surgical intervention. What we found over the past 10 years of using chemotherapy before surgery is that about 40% of the time, women who had evidence of lymph node involvement based on the biopsy will no longer have any disease in the lymph nodes at surgery, because the chemotherapy can eradicate the disease not only in the breast but also in the lymph nodes and other parts of the body. Now that this neoadjuvant chemotherapy has become more common in women with earlier-stage breast cancer, and we find that we are eradicating the disease more frequently, we wanted to see if we can use a less invasive approach after chemotherapy to see if we had eradicated the disease in the lymph nodes, and therefore, didn’t need to do a full axillary lymph node dissection.
This trial was designed to have women who had evidence of disease in the lymph nodes confirmed by needle biopsy receive chemotherapy. After chemotherapy, they were scheduled to have sentinel lymph node surgery at the same time as the axillary lymph node dissection, and then pathologists would assess how accurate the sentinel lymph node surgery was in determining the status of those lymph nodes. So, what we found was that 91% of the time the sentinel lymph node did reflect the status of the axilla. In women where the sentinel node was negative, the axilla was negative, and when the sentinel node was positive, the axillary lymph nodes were positive; it was accurate. But we know that in some women, the sentinel node was negative for any cancer, but there were axillary lymph nodes that had disease in them, meaning that was a false negative result, and that the sentinel node did not accurately stage the axilla.
The concern there, of course, is that you are leaving disease behind, if you did only the sentinel node surgery and the sentinel node was negative. This has always been a concern since this technique was developed—we knew that there was a chance of a false negative event. Several prospective trials have shown that if you pay attention to how the sentinel lymph node surgery is performed, you can reduce the chance that there will be a false negative result. That is why we had recommended that surgeons use both blue dye and radiolabeled colloid to perform the sentinel lymph node surgery, because we knew that reduces the false negative rate. We also knew that if you remove more than two sentinel nodes, it reduces the false negative rate. The reason for that is that most women do have more than one sentinel node. There are usually two or three, and most studies have shown that there are two or three, because the lymphatic drainage of the breast is quite complex. What we had recommended is that surgeons remove at least two sentinel nodes, not that they should randomly take additional nodes, but that they should really try to be very complete in the sentinel lymph node surgery before they went on to do the axillary lymph node dissection. Previous studies have shown that when surgeons are doing the sentinel node surgery at the same time as the axillary node dissection, oftentimes if they identify one central node, they will stop and then do the axillary node dissection, but we know that that will cause false negative events because the central node they recover may not have been the one that had metastatic disease at presentation, and they still may have disease on axillary lymph node dissection.
So, what we found is that the false negative rate was higher than what we had set as our predefined rate that we would accept, being 10%. We found a rate of 12.6%, but if we look at when the techniques were employed that we had recommended, namely dual agents for the mapping, and more than two sentinel nodes recovered, then the false negative rate falls below that preset endpoint.
Cancer Network: What are the implications of this study?
Dr. Hunt: I think the implications are that if the attention to the surgical procedure is carefully discerned by the surgeon, then we can use this technique for staging the axilla after chemotherapy. But the other thing that we found from this trial is that we need to select the patients very carefully. Just as we would select a patient for using chemotherapy or not, or using hormonal therapy or not, to treat their cancer, we need to select patients very carefully for this type of surgery as well. In other words, we would want to see that the patient had not only had the chemotherapy, but that the lymph nodes that were detected at that initial presentation do show evidence of response based on ultrasound and physical examination, whereas in the trial we are discussing, the patients were just selected based on having a lymph node that was identified at presentation, and then they had chemotherapy and surgery, and we did not exclude them if they still had evidence of disease based on ultrasound or other imaging techniques. The implications are that we can be less invasive with our surgical approaches, but we have to be careful in how we select our patients and how we perform the procedure, and that we are certain that we remove all of the sentinel nodes to be sure we are getting an accurate staging.
Cancer Network: Are there any studies that are following up on these results that you can highlight?
Dr. Hunt: There have been a couple recent studies showing that in women who present initially for breast surgery and have sentinel lymph node surgery and there is a positive sentinel node, if they are randomized to undergo axillary dissection versus axillary radiation, the axillary radiation appears to control any residual disease that might be there just as well as doing an axillary dissection. And it seems to have a lower rate of side effects, mainly lymphedema. One trial that we have that is now open, recently activated through the alliance for clinical trials in oncology, is a study in which we are assessing patients who present with node-positive disease, have chemotherapy, and then if after chemotherapy they had a good response in the lymph nodes, but we do a sentinel node biopsy and it still shows disease in the sentinel node, we are randomizing them to have axillary dissection versus radiation, because we think the radiation may have fewer side effects and will still be a good option for controlling any residual disease that might still be there.
Cancer Network: Thank you so much for joining us today, Dr. Hunt.
Dr. Hunt: Thank you.
- See more at: http://www.cancernetwork.com/podcasts/sentinel-lymph-node-surgery-breast-cancer?GUID=493C0B05-172C-4898-9E4B-DE045D6D2BF5&rememberme=1&ts=25102013#sthash.Wq91TFah.dpuf

Thursday 24 October 2013

Welcome to Linda Ikeji's Blog: Ex-PMAN president Mustapha Amego dies after battle with cancer

Welcome to Linda Ikeji's Blog: Ex-PMAN president Mustapha Amego dies after battle with cancer

ORANGE PEEL'S HEALTH BENEFIT TO CANCER TREATMENT


Orange peels are the thick finely-textured and orange coloured skin of oranges. Since ancient times, orange peels have been valued for their curative properties.
Many of us normally throw out the peels when it comes to oranges-whether we’re making fresh orange juice, snacking on whole oranges or making a yummy citrus salsa. But this is one big mistake as many of the highly nutritious compounds of oranges are found in the peels!

                                                  As an anti-cancer
Where there are antioxidants,there is the potential for a cancer fighting food. So peels recommended for those at high risk since the peel has a high conger bone concentration of antioxidants and flavonoids which have been shown to reduce cancer risk as well as be instrumental in the cure for the disease. It also cure some diseases like improvement on digestions,Cold,Anti-inflammatory,stronger bone,bad Breath e.t.c

                                                           Cautions 

Please ensure you purchase pesticides-free, organically grown oranges if you’re planning to consume orange peels. Many oranges today are grown chemically using pesticides or insecticides to thwart insects and other pests. These chemicals penetrate deep into the peels and are NOT good for you.

Saturday 19 October 2013

berries-foods-fight-cancerTo reduce your risk of cancer, look no further than your fridge. "All the studies on cancer and nutrition point to eating plant-based foods for their phytonutrients and other special compounds," says Richard Béliveau, PhD, chair in the prevention and treatment of cancer at the University of Québec at Montreal and author of Foods to Fight Cancer.

Aim for five to nine daily servings of all kinds of fruits and vegetables—especially these six superstars.

 broccoli-fights-cancer

Broccoli

All cruciferous veggies (think cauliflower, cabbage, kale) contain cancer-fighting properties, but broccoli is the only one with a sizable amount of sulforaphane, a particularly potent compound that boosts the body's protective enzymes and flushes out cancer-causing chemicals, says Jed Fahey, ScD. A recent University of Michigan study on mice found that sulforaphane also targets cancer stem cells—those that aid in tumor growth.

Helps fight: breast, liver, lung, prostate, skin, stomach, and bladder cancers

Your Rx: The more broccoli, the better, research suggests—so add it wherever you can, from salads to omelets to the top of your pizza.

  berries-phytonutrients-fight-cancer

Berries

All berries are packed with cancer-fighting phytonutrients. But black raspberries, in particular, contain very high concentrations of phytochemicals called anthocyanins, which slow down the growth of premalignant cells and keep new blood vessels from forming (and potentially feeding a cancerous tumor), according to Gary D. Stoner, PhD, a professor of internal medicine at The Ohio State University College of Medicine.

Helps fight: colon, esophageal, oral, and skin cancers

Your Rx: Stoner uses a concentrated berry powder in his studies but says a half-cup serving of berries a day may help your health too.

. tomatoes-lycopene-cancer

Tomatoes

This juicy fruit is the best dietary source of lycopene, a carotenoid that gives tomatoes their red hue, Béliveau says. And that's good news, because lycopene was found to stop endometrial cancer cell growth in a study in Nutrition and Cancer. Endometrial cancer causes nearly 8,000 deaths a year.

Helps fight: endometrial, lung, prostate, and stomach cancers

Your Rx: The biggest benefits come from cooked tomatoes (think pasta sauce!), since the heating process increases the amount of lycopene your body is able to absorb.
 walnuts-fight-cancer

Walnuts

Walnuts Their phytosterols (cholesterol-like molecules found in plants) have been shown to block estrogen receptors in breast cancer cells, possibly slowing the cells' growth, says Elaine Hardman, PhD, associate professor at Marshall University School of Medicine in Huntington, West Virginia.

Helps fight: breast and prostate cancers

Your Rx: Munching on an ounce of walnuts a day may yield the best benefits, Hardman's research found.

 garlic-fight-cancer

Garlic

Phytochemicals in garlic have been found to halt the formation of nitrosamines, carcinogens formed in the stomach (and in the intestines, in certain conditions) when you consume nitrates, a common food preservative, Béliveau says. In fact, the Iowa Women's Health Study found that women with the highest amounts of garlic in their diets had a 50 percent lower risk of certain colon cancers than women who ate the least.

Helps fight: breast, colon, esophageal, and stomach cancers

Your Rx: Chop a clove of fresh, crushed garlic (crushing helps release beneficial enzymes), and sprinkle it into that lycopene-rich tomato sauce while it simmers.

 black-navy-beans-fight-cancer

Beans

A study out of Michigan State University found that black and navy beans significantly reduced colon cancer incidence in rats, in part because a diet rich in the legumes increased levels of the fatty acid butyrate, which in high concentrations has protective effects against cancer growth. Another study, in the journal Crop Science, found dried beans particularly effective in preventing breast cancer in rats.

Helps fight: breast and colon cancers

Your Rx: Add a serving—a half-cup—of legumes a few times a week (either from a can or dry beans that've been soaked and cooked) to your usual rotation of greens or other veggies.
 meat-cheese-obesity-cancer

What not to eat: Animal fats

While researchers are still trying to determine which foods have the most cancer- preventing benefits, we do know what not to eat if you want to protect yourself, says Cheryl Forberg, RD, author of Positively Ageless:

Animal fats: Meat, cheese, and butter can be rich in saturated fat, which has been linked to obesity—a big cancer predictor. Opt for leaner protein sources, such as fish, low-fat dairy, and those good-for-you beans.

processed-foods-cancer-risk

What not to eat: Processed meats

A ballpark hot dog or a few slices of bacon once in a while won't kill you, but don't make them a staple of your diet. Some cured meats tend to be high in nitrites and nitrates, preservatives that can, in large amounts, potentially increase your risk of stomach and other cancers.

excessive-drinking-cancer-risk

What not to drink: Excessive alcohol

Stop after one drink! Too much tippling is associated with an increased risk of cancers of the mouth, esophagus, and breast.




Guyabano and cancer treatment through fruit like it....



guyabano(Natural News) The guyabano, or otherwise known as the custard apple or sour sop fruit, is deemed as one of the miracle cures for cancer. There have been various websites and claims that say that guyabano, from the tree, to its leaves, bark, and fruit, is capable of killing cancer cells naturally. A research that was conducted back in 1976 says that one chemical found in guyabano is about 10,000 times more powerful and potent than a drug used for chemotherapy called Adriamycin. This is why the Department of Science and Technology of the Philippines developed a supplement that is made from the guyabano fruit. Read on to find out more about this plant called guyabano.

What is the guyabano?

The guyabano (Anona muricata) is a tree that grows about five to seven meters high. It bears a pear-shaped fruit that is green in color and has soft spines. This tree is native to the Caribbean, Central America, South America, and African countries in the sub-Saharan area. The tree is also able to adapt to the tropical climate and could be found in most countries in Southeast Asia.

The matured fruit usually weighs about two to five kilograms and is ovoid in shape. The skin is thin and it has a whitish pulp that is soft, fleshy, and fibrous. The taste is distinct, with a tangy citrus taste. The fruits are harvested when they are mature, when the skin of the fruit is yellowish or shiny green in color.

The benefits of taking guyabano

The guyabano has been found to possess a lot of medicinal properties that a lot of people would definitely benefit from.

One article from 2008 in the African Journal of Traditional Complementary and Alternative Medicine reported that a study done on diabetes-mellitus afflicted rats that were fed with guyabano actually showed a significant lowering of their blood sugar levels. Separate studies conducted also showed the ability of guyabano in reducing alleviation, fever, asthma, arthritis, and skin infections. There are also studies that claim guyabano to be good for those who are suffering from herpes simplex infections, liver problems, and even hypertension.

Guyabano and cancer

There have also been studies that showed that those who took guyabano extract had better immune systems. The extract was shown to be helpful in targeting and killing cancer cells in about 12 types of cancer, including prostate, colon, pancreatic, breast, and lung cancer. The compounds in the extract have been proven to help in slowing down the growth of malignant cells, even better than the strong and commonly used chemotherapeutic agent, Adriamycin.

When people undergo chemotherapy, all the body systems suffer alongside the malignant cells. The guyabano extract's compound will selectively track and kill only the cancerous cells. The healthy cells are left alone. There have been studies conducted since 1976 that indicate guyabano is indeed a very good killer of cancer cells.

The claims still need to be backed by more studies, according to a lot of experts. There are a lot of people claiming that they have benefited from the extract, but there are still no recorded therapeutic claims from the use of guyabano extract.

Sunday 6 October 2013

Lung Cancer Therapy

ASCO: Treating Lung Cancer After Targeted Therapy–Resistance

By Howard West, MD1 | June 11, 2013
1Medical Oncologist, Swedish Cancer Institute, Seattle
Interviewed by Anna Azvolinsky, PhD


Howard West, MD Howard West, MD
AUDIO:
Download podcast (mp3)
Subscribe in iTunes
Today at the annual meeting of the American Society of Clinical Oncology, we are discussing targeted therapy strategies for lung cancer and dividing lung cancer patients into molecular subgroups with Dr. Howard West, a medical oncologist specializing in lung cancer at the Swedish Cancer Institute in Seattle, and founder and CEO of Global Resource for Advancing Cancer Education, or GRACE, a nonprofit that is providing up-to-date, high-quality information from cancer experts to patients and their caretakers. Dr. West is involved in both early- and late-stage clinical trials. At the ASCO meeting, he discussed how to manage advanced lung cancer patients after they stop responding to a targeted therapy.
Cancer Network: Dr. West, non–small-cell lung cancer is becoming increasingly defined by molecular subtypes. Could you go over what the established subtypes are and the available agents that target these?
(MORE: ASCO: Heat Shock Protein 90 Inhibitor Shows Promise in NSCLC)

Dr. West: Well, we are increasingly doing molecular testing on the vast majority of patients with non–small-cell lung cancer. When we talk about molecular testing, we are really focusing this point on patients with non–small-cell lung cancer subtypes, so the approximately 87% or 88% of lung cancer that is non–small-cell. Then, within that group, adenocarcinoma comprises about 60% or so of the patients in the United States, and most of our patients who have an actionable target have an adenocarcinoma, but there are some patients who have the squamous subtype, which is about 20% to 25% of non–small-cell, and they are less commonly found to have an actionable mutation and are a subgroup of patients that we don’t routinely send for molecular testing. There is another small group of patients who don’t fit into the adeno or squamous non–small-cell, and they have a variable probability of having mutations so we still test them. Specifically, the mutations we are looking for are EGFR, or the epidermal growth factor receptor, which is seen in about 10% to 15% of patients in North America and more like 25% to 30% of those in Asia—also ALK rearrangements, which occur in about 4% of patients with non–small-cell and predominantly those with adenocarcinoma. Both of these mutations are more commonly seen in patients with no smoking or minimal smoking history. Finally, there is a mutation called the ROS1 rearrangement that is less common, only about 1% of patients, and these patients seem to respond to the ALK inhibitor drug crizotinib that was approved for patients with the more common ALK rearrangement. So, this testing for ROS1 is not as prevalent yet, not as widely available but is increasingly being tested for, at least by many lung cancer specialists who have found patients who can benefit greatly from these treatments. Because when you do have a driver mutation and the right target, we see a probability of response and depth of response that we just don’t see with chemotherapy.
Cancer Network: So, what is the best time for patients to receive the targeted therapies you mentioned, the EGFR inhibitors and the ALK inhibitors?
Dr. West: In general, there is a consensus that we should be giving these therapies as early as possible, as soon as you know a patient has a mutation that could have a high association with a good response. The treatments that we are talking about in the United States, erlotinib for patients with EGFR mutations or crizotinib for patients with an ALK rearrangement, are oral therapies that are typically better tolerated than chemotherapy, or at least generally very well tolerated. They certainly lend themselves to longitudinal administration because they tend to not have many cumulative side effects. They give a high probability of response in the range of 60% to 75% and a degree of response that we just don’t see with standard chemotherapy. We do tend to favor these being the first therapy that you give if you find that a patient has one of these driver mutations before you start them on systemic therapy. We don’t have complete proof that it is better in terms of overall survival to give these therapies first rather than a maintenance therapy or second-line or later. I think many patients will do just as well if they end up getting these very effective drugs as second-line or later therapy. But, unfortunately, some patients do have unforeseen and catastrophic complications—perhaps leptomeningeal disease, which is involvement of the brain with the cancer that can lead to a rapid decline. Patients can miss that opportunity for treatment that can produce rapid and long-lasting responses, and that is exactly what we want to avoid. So, in general, just about everybody is inclined to give the drugs early on.
Cancer Network: How long do patients generally respond to EGFR inhibitors or crizotinib, and is there a way to predict response length?
Dr. West: There is not a good way to predict this in both EGFR mutation patients and those with an ALK rearrangement. The median duration of response before patients progress is in the range of 8 to 12 months, varying from one patient to another. Typically within a year, but there are a minority of patients who continue to do well for several years at a time, even a few beyond 3 or 4 years. There is a little bit of evidence that is not as consistently reported that patients with a particular mutation in EGFR, called exon 19, have the greatest probability of prolonged response compared with those with another activating mutation on exon 21. But, that is about the only predictive marker we have and even that is not that consistent, so we really can’t say whether someone is likely to respond for a few months or several years to these agents. That said, the degree of response that we see in a patient tends to be correlated with how well they do, so the patients who immediately feel better and whose imaging shows a dramatic response are also often the patients who have the longest responses.
Cancer Network: Most patients’ tumors eventually acquire resistance to the targeted therapies you mentioned. How is resistance typically detected and defined, and what are the issues with defining resistance in the clinic?
Dr. West: Resistance is typically detected by routine imaging. When we are following someone with lung cancer and we do chest CT scans or sometimes PET-CT every few months, we will generally see a new lesion in the liver, the lungs, or the bone, or a growing lesion that we have been following for a while. If the changes are significant enough, that will be considered progressing disease; it has to do with the dimensions of the tumor. It is important to recognize that small subtle changes, or even a new lesion or two, don’t necessarily lead most experts to want to make a change in therapy. We can see very slow, indolent, and not clinically significant progression of disease long before a patient actually needs to make any change at all. Many patients will go 3 months, 6 months, even a year or longer before they have enough change that the treating physician with a lot of experience concludes that there is an incentive to make a change in treatment—whether that is discontinuing the targeted therapy and making a switch to chemotherapy, or adding chemotherapy and continuing the targeted therapy. There are also some patients who will have new symptoms related to their cancer, whether an area of pain from a bone lesion or new headaches, vision changes that lead to a head MRI and show that someone has a new brain metastases, that are of course clinically significant. But with regards to brain lesions in particular, many experts are really not inclined to discontinue the targeted therapy because brain lesions that arise in this setting don’t necessarily represent resistance to the drug as much as the drug just not being able to get into the central nervous system. Many of these patients can be treated for their brain metastases, with radiation for instance, and continue to do extremely well for months or even years on the ongoing targeted therapy.
Cancer Network: What are the current treatment options for patients who do become resistant to targeted agents? Is it mostly chemotherapy?
Dr. West: Well, there are a growing number of clinical trials, sometimes with novel agents, and certainly these are very appealing options when they are available. Outside of that, we do generally favor chemotherapy. If patients have received first-line targeted therapy, then we generally try to approach treatment with the same chemotherapy options as for someone who is being treated in the first-line setting and who doesn’t have a mutation. Typically, this would be a platinum-based doublet, potentially with bevacizumab(Drug information on bevacizumab), the antiangiogenic agent. Some experts favor continuing the EGFR or ALK inhibitor, and some favor discontinuing it and even potentially restarting it later because we sometimes do see responses or at least prolonged stable disease after rechallenging the patient, even with a drug that they had progressed on earlier because sometimes patients’ tumors can become resensitized to that targeted therapy after a period off of these drugs.
Cancer Network: Lastly, are there any issues with developing resistance to targeted therapies and treatment of patients that we haven’t touched upon yet?
Dr. West: I would say that there is a lot of controversy about whether repeat biopsies should be done in all patients, whether this is a desirable option or whether this should really be bothered with at all. We will sometimes see a change in the histology of the cancer from non–small-cell lung cancer to small-cell lung cancer in somewhere between 3% to 14% of patients who develop resistance. This was actually a very hard to believe finding when it was first reported several years ago, but it has been confirmed by several different studies. You can sometimes see small-cell lung cancer lesions that developed while the patient was on an EGFR inhibitor for months or years, and these patients even have EGFR mutations in non–small-cell lung cancer, so it seems to be an actual transformation. Many of these patients can respond very well to the chemotherapy approaches used routinely for small-cell lung cancer, which is typically a platinum drug with etoposide(Drug information on etoposide) in North America. So, that is one incentive to potentially do a biopsy on a progressing lesion. But, that is also a minority of patients. Outside of that, we really don’t have examples of an actionable result that will lead to a change in treatment based on a biopsy. I don’t consider this a standard of care. That said, I do favor getting tissue whenever possible because this has been the way the field has moved forward to understand the molecular mechanisms underpinning acquired resistance. There have been a growing number of clinical trials with targeted therapies that require tissue. I would say that our biggest advances that we have made in the field in non–small-cell lung cancer have been based on molecular oncology, so the limitation of not having enough tissue is going to limit our understanding and the availability of new therapies. The best thing we can do, even if it is not yet the standard of care, is to get more tissue to try to understand things better.
Cancer Network: Thank you so much for joining us today, Dr. West.
Dr. West: Take care.

Asymptomatic Navel Lump

A 74-Year-Old Caucasian Man Presents With Asymptomatic Navel “Lump”

Professor of Dermatology at Baylor College of Medicine; Chief of Dermatology at Michael E. DeBakey VA Medical Center



A 74-year-old, previously healthy, nonsmoking Caucasian male presented with a 4-month history of an asymptomatic “lump” in the navel. Review of systems revealed an involuntary 17-pound weight loss during the previous 6 months and intermittent localized abdominal pain of mild to moderate severity. Recent routine laboratory values and chest radiograph were within normal limits. A carcinoembryonic antigen (CEA) level was 55 ng/mL (severely elevated). A fecal occult blood test was positive. Physical examination disclosed a firm 3.5 cm × 3 cm violaceous nodule occupying the central umbilicus, surrounded by a narrow rim of similarly colored, indurated periumbilical skin. Biopsy of the umbilical nodule revealed adenocarcinoma.

Comprehensive Ways to Heal Cancer

    An understanding and very open ways of healing cancer goes on these eight factors:
  • A positive attitude
  • Detoxification
  • Immune Building
  • Life time changes
  • Natural Chemotherapy
  • Oxygen Therapy
  • Proper Nutrition and Clean Water
      With these ailment to cancer may be reduce in the system of human body if persist on these routine....