Abrupt Turnabout in PARP Inhibitors

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  • Member_of_the_Club
    Member_of_the_Club Member Posts: 3,646
    edited February 2011

    PLease keep in mind that PARP inhibitors have only been used in women with metastatic disease who are triple negative and have few options.  They gave women who had little hope, some hope and I'm sure the latest results are devastating.  I'm sorry, but your post seems to almost be gloating  about a treatment that has failed and therefore somehow supports your anti-chemo bias.  Fine to have that bias, but in this context it seems cruel.

  • mollyann
    mollyann Member Posts: 472
    edited February 2011

    Yazmin is posting a report that is in the news section of breastcancer.org How is that a bias? When are facts a bias? 

    Maybe you should contact breastcancer.org's news division and tell them to cover up the failures of PARP chemo?

  • Member_of_the_Club
    Member_of_the_Club Member Posts: 3,646
    edited February 2011

    More food for thought? In other words, another chemo failure.  There are very few women on the alt boards who have metastatic disease, so who is she posting this for?  Its on the home page, why else would she be posting.I remember on the stage IV boards when the trials for PARP inhibitors started and how incredibly hopeful those women are, how thrilled were the women who made it into those trials.  So when I saw the report all I could think was how heartbreaking this is going to be for those women, and for the other women with metastatic disease who hoped this treatment would save their lives.

    Its gloating and I'm sorry but its cruel. 

      

  • mollyann
    mollyann Member Posts: 472
    edited February 2011

    Member, I don't know why you would attribute such an unkind emotion as gloating to posting the PARP report.

    I'm saying this to you as I would a friend in the room with me. Everybody on this board wanted the PARP therapy to work for these women. We want everything everybody does to work for them. No one is gloating. We are not rivals, we're all in this together. I'm disappointed PARP didn't work. I'm truly sad. It brings tears to my eyes.

  • Member_of_the_Club
    Member_of_the_Club Member Posts: 3,646
    edited February 2011

    I believe you.  But what did she mean by more food for thought -- more -- if she wasn't referring back to prior posts against chemo.  There are no women on the alt boards in the PARP trial or considering PARP.  Perhaps gloating was too strong a word, but still.  The post really disturbed me.

  • luv_gardening
    luv_gardening Member Posts: 1,393
    edited February 2011

    Thanks Yasmin, I'd been avoiding clicking on the BCO link as I knew it would be upsetting to see a hopeful drug not coming up to expectations.  Who knows whether these drugs, if they worked, could be adapted to be used by all BC stages and varieties and could one day save or extend many lives.  We all have a stake in them working.

    Food for thought.  Some of my thoughts in no particular order:

    I wonder if the further ongoing studies will have a more favourable outcome?

    Was there some problem with the study to cause a disappointing result?

    The women still increased overall survival by almost 5 months so it's hard to understand why this is not statistically significant.  Does this mean they can go ahead and release the drug on the market or do they need better outcomes from the remaining studies?  I've seen many drug released that only increased OS by 2 or 3 months in other cancers.

    Maybe some tweaking of these drugs or how they are used will have the desired results and this will propel them to do that.

    The article says women can still enrol for ongoing clinical trials, but clearly they may not be able to get in one.  This is more than sad for those who were pinning their hopes on a successful outcome.

    The article is not really informative enough for those of us who don't understand the implications of these studies and the drug approval process.  I'd like to know a lot more.

  • elmcity69
    elmcity69 Member Posts: 998
    edited February 2011

    I agree with Member of the Club. it's hard to exactly enunciate why....it seems irrelevant, really, to post this, unless one is specifically affected by this issue (triple neg, metastatic disease).

     why is this tx failure food for thought, Yazmin? this isn't a sarcastic question, but an earnest one. Is it pointing at the various failures of Western medicine? or sympathetic to the patient population?

    i'm curious.

  • motherofpatient
    motherofpatient Member Posts: 240
    edited February 2011

    Check this out - PARP may still be a good option for some triple negatives and many other companies are partnering with Sanofi-Aventis on this.Seems they tried to cover too much ground in one study.

    http://www.genomeweb.com/dxpgx/missed-opportunity-would-pgx-have-helped-sanofi-aventis-avoid-phase-iii-failure

  • Member_of_the_Club
    Member_of_the_Club Member Posts: 3,646
    edited February 2011

    I know that there are some women in the stage IV section who have had a positive response, so I do hope they continue to pursue it. 

  • MJLToday
    MJLToday Member Posts: 2,068
    edited February 2011

    Yes Motherofpatient, I believe the drug developer just got greedy with wanting to market this drug to too many people.  So, now, there is going to be a delay in FDA approval, and a probably people dying that could otherwise benefit from the approval of this drug.

    See this op-ed for a good perspective on this phenomenon:

    http://www.forbes.com/forbes/2011/0228/technology-adriana-jenkins-cancer-herceptin-dying-wish.html 

  • Yazmin
    Yazmin Member Posts: 840
    edited February 2011

    Yes, MJLT, I also believe that the drug developer just got greedy with wanting to market this drug to too many people.

    Just as I believe that drug developers got greedy wanting to market "automatic" chemotherapy to too many people. And wanting to market SERMs and AIs to too many people. Clearly, these drugs benefit some people (albeit not as much as we, cancer survivors, would like).

    In my case, I was given the TAC chemo, and around the end of it, was told (by outstanding mainstream oncologists) that it has now been firmly established that chemo does not benefit

    my tumor type (ER+, PR+, HER-). This happened in 2006: see the article below, from one of my local newspapers, and dated 2006.

    I know, I know: I can understand why such news can upset some people: it would be so much nicer if new and established treatments clearly benefitted us, cancer patients. These news are upsetting to me, as well, believe me...... 

     -----------------------------------------------------------------------------------------------------------------------------------------

    Shift in Treating Breast Cancer Is Under Debate

    ·   By GINA KOLATA

    Published: May 12, 2006

    Doctors who treat women with breast cancer are glimpsing the possibility of a vastly different future. After years of adding more and more to the regimen — more drugs, shorter intervals between chemotherapy sessions, higher doses, longer periods of a harsh therapy — they are now wondering whether many women could skip chemotherapy altogether.

    Michael Stravato for The New York Times

    Janice Baty, a mother of two children, was told by her doctor that she might not need chemotherapy. But she chose it anyway, feeling safer.

    E-mail Gina Kolata at: kolata@nytimes.com

    Related

    Studies Challenge Traditional Breast Cancer Treatments (April 12, 2006)

    Multimedia

    Video: New Ideas on ChemotherapyIf the new ideas, supported by a recent report, are validated by large studies like two that are just beginning, the treatment of breast cancer will markedly change.

    Today, national guidelines call for giving chemotherapy to almost all of the nearly 200,000 women a year whose illness is diagnosed as breast cancer. In the new approach, chemotherapy would be mostly for the 30 percent of women whose breast cancer is not fueled by estrogen.

    So far the data are tantalizing, but the evidence is very new and still in flux. And even if some women with hormone-dependent tumors can skip chemotherapy, no one can yet say for sure which women they might be. Some doctors have already cut back on chemotherapy, but the advice a woman gets often depends on which doctor she sees.

    It could be a decade before the new studies — one American, one European — provide any answers.

    "It's a slightly uncomfortable time," said Dr. Eric P. Winer, who directs the breast oncology center at the Dana-Farber Cancer Institute in Boston. "Some of us feel like we have enough information to start backing off on chemotherapy in selected patients, and others are less convinced."

    Among the less convinced is Dr. John H. Glick, director of the Abramson Cancer Center of the University of Pennsylvania. Dr. Glick tells his patients about the new data but does not suggest they skip chemotherapy. After all, he notes, the national guidelines were based on results from large randomized clinical trials. And the recent data indicating that some women can skip chemotherapy are based on an after-the-fact analysis of selected clinical trials.

    "We're in an era where evidence-based medicine should govern practice," Dr. Glick said.

    For women with breast cancer, of course, the uncertainty is excruciating. Faced with a disease that already causes indecision and anxiety, they are now confronted with incomplete data, differing opinions from different doctors and a choice that can seem almost impossible: Should they give up a taxing treatment when all the answers are not in and they have what may be a fatal disease?

    "If the medical profession is not even close to being of one mind, how is the woman to know?" said Donald A. Berry, a statistician at the University of Texas M. D. Anderson Cancer Center, the lead author of a recent paper questioning chemotherapy's benefits in many women.

    Barbara Brenner, who has had breast cancer and is executive director of the advocacy group Breast Cancer Action, said, "There's a real problem," and added, "We finally tell people at the end of the day: 'You're going to get a lot of information. Trust your gut. Nobody has the answers.' "

    "I'm really glad I was diagnosed 13 years ago," Ms. Brenner said, "when there were fewer choices."

    Doctors worry, too. It took two years before the National Cancer Institute and its researchers could even agree on a design for the large new American study that will test the idea that many women might safely forgo chemotherapy.

    The study, which starts enrolling patients at the end of this month, will involve women whose cancers are fueled by estrogen and have not spread beyond the breast. They will be randomly assigned to have the standard treatment — chemotherapy followed by a drug like tamoxifen that starves tumors of estrogen — or to skip chemotherapy and have treatment only with a drug like tamoxifen.

    Unlike the American study, the one now planned in Europe will also include women whose cancer has spread beyond their breasts into nearby lymph nodes. The American study may eventually add such women, said Sheila E. Taube, who directs the cancer diagnosis program at the National Cancer Institute.

    Dr. Taube said the debate reminded her of one a few decades ago, when the question was whether all women with cancer needed mastectomies or whether many could have a lumpectomy instead. "To me, the situations are analogous," she said.

    The chemotherapy question starts with American and European guidelines that say almost every woman with breast cancer that has gone beyond its earliest stages, when it is confined to the milk duct, should have the treatment. And for good reason, many cancer researchers say: a series of large studies has shown that chemotherapy saves lives and that newer and more aggressive regimens are improvements over older ones.

    That has led doctors to feel most at ease giving very aggressive treatments to almost everyone.


    Shift in Treating Breast Cancer Is Under Debate

    ·   

    PPublished: May 12, 2006

    (Page 2 of 2)

    "Part of it is that this area of medicine we're practicing in is kind of a high wire act," said Dr. Michael Lee, an oncologist in private practice in Norfolk, Va. "It is more comfortable to adopt things that are aggressive."

    Skip to next paragraph

    E-mail Gina Kolata at: kolata@nytimes.com

    Related

    Studies Challenge Traditional Breast Cancer Treatments (April 12, 2006)

    Multimedia

    Video: New Ideas on Chemotherapy

    But most of those studies were done at a time when doctors did not distinguish between the 70 percent of women with breast cancers fueled by estrogen and the 30 percent whose cancers were not.

    Now Dr. Berry, the M. D. Anderson statistician, and a group of leading cancer researchers have found that the chemotherapy benefits in those clinical trials were concentrated almost exclusively in women whose cancers were impervious to estrogen. For the others, with estrogen-sensitive tumors, the lifesaving benefit came from hormonal therapy. The results of the analysis, published recently in The Journal of the American Medical Association, were the same even if the cancer had spread to the lymph nodes.

    The drawback of that study, Dr. Glick notes, is that it was not a large prospective randomized clinical trial, the gold standard in medicine.

    There is also another issue. What if some women with estrogen-fed tumors do benefit from chemotherapy? How can they be identified?

    One possibility is new genetic tests, which are part of the two studies that are about to begin. The cancer institute is using the Oncotype DX test, which includes genes associated with response to chemotherapy, among them genes involved with a cell's response to estrogen.

    The study is ethical, said Dr. Larry Norton of Memorial Sloan-Kettering Cancer Center in New York, because the only women whose treatment will be decided at random are those in a kind of gray area, not women for whom chemotherapy would be a clear benefit or clearly unnecessary.

    "I think the clinical trial is really a superb one," Dr. Norton said. "I would like to see it go so we have definitive data."

    In the meantime, some physicians, like Dr. Winer, are taking their own best shot at figuring out who really benefits from chemotherapy. He asks how sensitive the tumor is to estrogen, how aggressive a pathologist believes it is, how big it is, how much has spread to the lymph nodes and whether its surface has a type of protein, HER2, that is associated with a better response to chemotherapy. After talking through the decision with his patients, he says, he is comfortable omitting chemotherapy in some who would have had it not long ago.

    Others, like Dr. Francisco J. Esteva of M. D. Anderson, use a computer program to calculate a woman's risks of recurrence and give the option of no chemotherapy only to women with low-risk cancers confined to their breasts.

    Still others, like Dr. Glick, are starting to tell women with estrogen-fed cancers that although they still need chemotherapy, they may not need the most intense treatment.

    And while some, including Dr. Winer, predict that the use of chemotherapy will almost certainly decline in the years ahead, for now most doctors are sticking with the current guidelines, waiting for expert advice from national panels on what to do.

    "I don't know that many doctors who are comfortable giving women an option about chemotherapy," said Fran Visco, president of the National Breast Cancer Coalition, an advocacy group. "A lot of physicians talk about the data, but then they say, 'But, to be on the safe side. ...' "

    Still, doctors say it is not simply that they are urging more and more chemotherapy on patients. In many cases, it is patients who want the most aggressive treatment.

    "A cancer diagnosis is earth-shattering," said Dr. Lee, who has had cancer himself. "You stay up at night. You wonder. Even when you're doing well, you don't know whether to trust it."

    And so, he said, "a lot of people will take a treatment even if there is a very low statistical chance that they will benefit."

    That was what happened a few months ago, when Dr. Esteva told Janice Baty of Sulphur, La., a 40-year-old mother of two, that she might not need chemotherapy. After a long discussion with Ms. Baty and her husband, Dr. Esteva left them so they could decide what to do.

    "My husband said, 'Look, we have two little kids,' " Ms. Baty recalled. "I called the doctor back in and said, 'We're doing the chemo.' "

    Women who say they want the most aggressive treatment may not fully realize what they are asking for, said Mary Peelen, 45, of San Francisco. Ms. Peelen learned in January 2005 that she had cancer. It was small, was fed by estrogen and had spread to just two of her lymph nodes. Her oncologist was adamant: chemotherapy was her only option.

    "I felt frightened and very coerced," she said. She had an aggressive regimen, suffered terribly and was left with painful nerve damage in her arms and hands that prevents movements like opening jars or using scissors and frequently makes her drop things.

    Ms. Peelen feels that in a way, she just missed the revolution, perhaps one of the last women with her type of cancer who will have to suffer so much.

    For now, the answers as to who should have chemotherapy are far from clear.

    "I think practice should change, but it's very dicey," said Dr. Berry, of M. D. Anderson.

    His colleague Dr. Esteva says it is one thing for a statistician like Dr. Berry to look at retrospective data, and another for a physician, like himself, to sit down with a patient who has to make what may be a life-or-death decision.

    "It's not a perfect science," Dr. Esteva said. "A statistically small reduction in risk may be very important to some women, while for others chemotherapy is not worth it."

    And so, Dr. Esteva said, he is left asking many women with early-stage breast cancer to decide what can seem like the undecidable: whether they want "to take something potentially toxic when you have a 90 percent chance of being cured without it."

    "My experience ," he said, "is that more want to get chemo than not 

  • Member_of_the_Club
    Member_of_the_Club Member Posts: 3,646
    edited February 2011

    It has not been "firmly established" that chemotherapy does not work on er/pr+ tumors, only that it is over prescribed, which we knew.  There will always be women who have chemo who would have survived without it and its terrific that they are getting better and better at determining who those women are.  But I don't think hormone status is enough to make that call.  There are hormone positive tumors that are more aggressive.

     I had a tumor marker test that was done while I was in chemo and it was quite elevated.  This caused me a great deal of anxiety as you can imagine, until after chemo when it went back down to the normal range.  What I learned is that markers can be elevated by the cancer cells dying off, which is why it can be elevated during chemo.  I believe this was a sign of the chemo working for me.  This is obviously not proof -- maybe it was elevated for some other reason (but it was over 70, so quite elevated).  But it seemed like a pretty strong indication to me.

    They just do not know with any specificity what benefits whom, so we go by numbers and stats and we make our personal decisions accordingly.  I am willing to live with the risk associated with a small benefit because of my children.  And as I said, i believe in my case the benefit was actually substantial. 

  • luv_gardening
    luv_gardening Member Posts: 1,393
    edited February 2011

    The way I see it, (purely conjecture from a lot of reading), after surgery there are at least four possibilities but limited means of knowing which applies.

    1- Clear - the cancer has not spread beyond the removed tissue, no stem cells have escaped or other means of spread, therefore chemotherapy would be pointless.

    2- Seeded- cancer has seeded beyond the excised tissue and is either waiting in the bone marrow or wherever it hides, out of reach of chemotherapy and blood tests, but no mets have started to form yet.

    3- Metastasis- mets have begun and may be well developed or microscopic. Those metastasis may be shrunk by chemo but some stem cells will remain to start growing again. This group will progress sooner without chemo but as current chemotherapy cannot cure mets, they will eventually succumb if they don't die from something else first.

    4- Early Cells - the tumours have all been surgically removed but some cells have entered the blood stream either from the surgery, biopsy or independently from any procedures. These are the ones that chemo can obliterate and a cure happen if the right chemo is used at the right time as these cells start to divide. Even with chemo, some may not be successful as we are really using hit or miss tactics with the choice of chemo till better tools are found to select the best drugs for each individual.

    5- IBC  Edited to agree with Black Cat that in the case of IBC and possibly other variants, (possibly hormone negative), there is no doubt that chemo saves lives and is urgently required before all other treatments for IBC.

    So in my opinion the third group will have some benefit by delaying the inevitable, and the question is, can this be achieved some other way to save people from the side effects and very real dangers of chemotherapy.

    The urgency is to find out which group each cancer falls into by developing a blood, bone marrow or other test that is reliable. Without sophisticated tests we are really working in the dark, not knowing which chemo if any, is needed, whether it is helping or to what extent.  For those in the second group (Seeded) we need to find a way to kill off stem cells to effect a cure or long term treatment by stopping mets from ever developing.

    Dormancy- I am also intrigued by the fact some cancers can seem to remain dormant for decades. I realise that they may just be slow growing, but I feel there must be some way we can delay the onset of new growth. We should be able to keep the stem cells or whatever means they use to seed themselves in a dormant phase so we can remain free of mets.

    Meanwhile, as MotC said so well, we go by stats as it's the best we have though I believe it's a massively clumsy tool at the moment and these new studies should make a big difference to the data.

    I must stress again that the above is purely conjecture from the reading I have done and I am not in any way trained in science or critical thinking and welcome any informed discussion or respectful disagreement. 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited February 2011

    Chemotherapy saved my life.  Not too long ago the protocal for inflammatory breast cancer was surgery first. The fatality rate was 100%. This is due to IBC being a very agressive cancer that grows in sheets and spreads to the skin.  Now the protocol is chemo first to shrink the cancer and get it out of the skin.  I am ER+ /PR+/ HER2- and chemo not only erradicated the cancer from my skin but shrunk a 7 cm tumor down to 3 cm.   The ACT chemo protocal worked for me.  It was no walk in the park but it was well worth it.

  • luv_gardening
    luv_gardening Member Posts: 1,393
    edited February 2011

    Yazmin,  thanks so much for posting those articles.  I wish I had read them long ago and am still trying to read them a bit at a time as it's a lot to take in and my head's spinning.

    Those studies to test if chemo is really making any difference are long overdue but wonderful news and also confirm that I have had good reason to doubt the use of chemo (except for IBC where it is essential).  I read quite a bit on the subject when various family members had cancer and was against chemo as I felt it was a long shot whether it worked and no proof either way.  I'm afraid  I just don't trust the adjuvant statistics as I feel they may be built on inadequate data and biased studies but I understand the intent of the studies and our specialists is all good and deeply respect those who are willing to brave chemo. 

    When I was faced with cancer myself with 9 nodes involved I had to make the scary decision about chemo and spent 7 days crying, the only time I broke down in the entire diagnosis and treatment time.  I ended up having the first two infusions of FEC but then opted out of any more as my instincts were screaming at me to stop.  So this whole subject is very close to my heart after the dire warnings from all my health providers at the time.  They are all very respectful and encouraging now and I thank them for that.  There are no rights or wrongs with primary chemo for many cancers as it's all still a mystery.

    I also believe the 4th group above,  Early Cells, is the understanding of oncologists and I doubt there are more than a tiny minority that will fall into this curable group, but I hope I am wrong.  I wish chemo was the cure and we could enter into it knowing we could be cured and free from the fear of progression.

    The third group, metastasis, I think will return either sooner or later depending on how large or aggressive the tumours are.  The research so far seems to show that the larger the tumour and the higher the grade, the more stem cells will be left to reseed new tumours so the chemo seems to me to only have limited effect.

    I look forward to refining my understanding of this subject and would love any links to studies that confirm, add to or subtract from my understanding.

    Black cat, I just saw your post after hitting "preview".  I should add IBC as a separate category as it clearly has it's own path.  Yes, chemo all the way for IBC.  Thank goodness it has such an important role for our IBC sisters and saved your life.  Fantastic. I will edit my above post.

  • Lynn18
    Lynn18 Member Posts: 416
    edited February 2011

    I agree with Member's comments; I don't understand the meaning behind this post.  Specifically, what does the poster mean by "more food for thought".  It it turns out the PARP does not work as well as we had hoped, it would indeed be a tragedy, especially for those of us who are triple negative.  So you are using this tragedy to make your point?  Is the point that chemo does not work?   -- Just trying to understand.

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