BC Drugs Urged for Healthy, High Risk Women - NYT
Yikes! Tamoxifen use can also make people triple neg. Very irresponsible of the task force, IMO. Again, prescribing one course of action for everyone in a subgroup when individuals in this subgroup may vary. No wonder we don't have a cure. Also, what part of the word "risk" do these people not understand? Risk is NOT certainty. There is no way to predict other risks.
This is fear-based medicine, IMO.
Now are at-risk woimen who refuse Tamoxifen going to be blamed if they get cancer? (With no individual science to back such a blame?)
Comments
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...and the risk assessment tool these bozos partly relied on was the same one that gave me a 0.8 percent chance of getting bc on the eve of my dx....
**head desk**
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Athena, I've already had ovarian cancer and a pulmonary embolism along with it. I have LCIS & lobular is notoriously hard to detect. I am upset that I CAN'T take Evista because of the clotting risk. As I am high risk I would welcome the educated decision to be able to take the preventative. It certainly wouldn't be a fear-based and knee-jerk decision on my part.
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Melissa - the point is not what it would do to you or another individual - the problem is telling millions of women the same thing, when only a few have the exact characteristics of the patient (such as yourself) that might benefit. So I appreciate that it would be good for you, but this is a nationwide recommendation.
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From the NYTimes article:
"The group estimated that among 1,000 women with an increased risk of breast cancer, there would be 23.5 cases of invasive breast cancer over five years. If the women took one of the drugs, 7 to 9 cases would be prevented over five years.
But an extra 4 to 7 women per 1,000 taking the drugs would develop blood clots during that time, and there would be 4 extra cases of uterine cancer per 1,000 women taking tamoxifen — an approximate doubling of both of those risks."
Okay, so let's do the math on this.
Without these drugs, 23.5 of the 1000 women will get breast cancer over 5 years. So this means that 976.5 women of the 1000 will not get breast cancer.
With these drugs, 7 - 9 cases of breast cancer will be prevented over 5 years. But this also means that 14.5 - 16.5 of the women will take these drugs and they will still develop breast cancer, plus they will have exposed themselves to additional serious health risks by taking these drugs and they will have experienced the quality of life side effects from taking these drugs. And the 976.5 women who never would have gotten BC anyway will also have exposed themselves to the risks and experienced the side effects.
Of the 1000 women who take these drugs, 4 to 7 women will develop blood clots and 4 will develop uterine cancer (women who would otherwise not have experienced these health issues). So this means that 8 to 11 women will experience these particular side effects...although I suppose it could be less if it happens to be some of the same women develop both of these conditions together.
To net it out:
* 1000 women take the drug.
* 991 - 993 of the women really didn't need to take the drug because they either weren't going to develop BC anyway or because they will develop BC whether they take the drug or not.
* 7 - 9 women avoid a diagnosis of breast cancer.
* 8 - 11 experience serious health side effects.
I have nothing against these drugs. If you've been diagnosed with BC and you have a high risk of recurrence - and particularly, a distant recurrence - these drugs can be life-saving. But the risk vs. benefit equation isn't quite a clear for those who have low risk diagnoses and those who have not been diagnosed but are high risk. It really depends on your recurrence risk level and/or your breast cancer risk level, as well as your risk level for these other conditions. "High risk" is a big tent, and having a small area of ADH (or even DCIS) or a 2nd degree relative with BC is a lot different than having a high risk diagnosis of LCIS or being BRCA positive. Unfortunately, it seems that there are too many oncologists who recommend these drugs without taking these important individual factors into consideration.
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I posted my opinion of the study in the comments section of the NYT. It said this (sorry - feeling too lazy to redo here):
I think the task force's recommendations are irresponsible. Let me count the ways....
--They are doing a count - a casino count, basically. Risk is NOT the same as certainty. It is well known that calculations based on retrospective data can yield wildly inaccurate results even in the best of hands because the data has not been "controlled" at all stages of the process.
--A high number of breast cancer cases are NOT hormone dependent.
--Many cancers treated with Tamoxifen may change receptor status - you see this in metastatic patients.
--The online tool, which the NCI itself cautions should not be used to determine individual cases, gave me a 0.8 percent chance of getting breast cancer - on the eve of my diagnosis.
--Women who may understandably be wary of taking these drugs, then develop breast cancer, may face blame for "not preventing" their cancer, when there is NO science to back such a supposition in individual cases.
Once again, a very diverse sub-group of patients is being treated with one broad brush stroke. Then we wonder why there isn't a cure for breast cancer more than 40 years after Nixon declared a War on Cancer.....Wonder no more. Numbers games don't work. Only pure science in the laboratory does. This is a step back for science and a lunge forward for guesswork. -
One thing to keep in mind, as well, is that - even without tamoxifen - breast cancer cells can- and do spontaneously change receptors. A friend of mine, who refused tamoxifen the first time for her hormone positive breast cancer, developed a recurrence three years later in the mastectomy scar that was hormone negative. It can happen. So, we need to know 1) how often this happens spontaneously vs 2) how often it happens as a result of tamoxifen and is the difference statistically significant.
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