Aromasin for LCIS
I have been diagnosed with LCIS. Thank God it is not more serious. I realize in the scheme of things this in the least of everyone's concerns, but I just would like to know if anyone has been put directly on Aromasin after being told you have LCIS? I an post menopausal 52 yrs old, and my doctor wants to put me on this for five years. (I have not taken Tamoxifen since I was diagonosed after menopause, they are prescribing Aromasin.) There is not much out there just one clinical trial. The results seem encouraging. Does anyone have any experiance with using this drug in this way?
Thanks for any info you can provide.
Comments
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I read the study and the results do look encouraging ( I think it said 65% reduction with aromasin versus 50% with tamoxifen and 38% with evista--correct me if I'm wrong). However, I already took the tamox for the full 5 years and now have been on evista for over 2.5 years (was diagnosed with LCIS 8 years ago). I'm wondering if my new oncologist will bring up aromasin at my Dec. visit. Fortunately, I've been able to tolerate both meds well with minimal SEs, so at this point, I really don't want to start a new medication with other possible SEs. Are you going to be having close monitoring as well? I continue with alternating mammos and MRIs every 6 months with breast exams on the opposite 6 months. Let us know how it goes.
Anne
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Thank you such a quick response. Yes I will have close monitoring. I am not looking forward to the SE put they will pass. I guess I have decided to take the aromasin. Did your treatment work for you? Seven and a half years is a long time to have to take meds. I hope your oncologist appointment goes well for you.
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I will probably be on meds indefinitely, as the risk will LCIS does NOT go down over time. Fortunately, evista is probably something I can take for the long haul, as it is actually an osteoporosis medication. (no time limit as far as I know, like there is with tamox or AIs) I have been doing very well for 8 years with no further bisopsies needed. (they are not necessarily a "given" just because one gets a diagnosis of LCIS; although some do end up having repeated biopsies for various issues), If I was to need more biopsies, I might seriously consider PBMs, but not interested in that route at this point.
Anne
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What kind of SE's does this drug have compared to tamoxifen & evista?
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Here's a link to the Aromasin package insert. See the 1st page upper right corner. Table 2 has side effects in early breast cancer vs. tamoxifen. http://labeling.pfizer.com/showlabeling.aspx?id=523
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I've been offered Aromasin and am still thinking about it. Can't have Tamox or Evista because of the clotting risk since I had a pulmonary embolism.
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I'm still confused about LCIS being called breast cancer. I was told by two surgeons that it is a marker for possible future cancer, not cancer. One oncologist I saw said it was cancer, one said it was not cancer. It seems still that doctors just can't seem to agree on what this is.
Has anyone been sent for pet scans, or other types of scans after their LCIS diagnosis? I have a 6 month left breast only mammo coming up, and honestly, I feel like I just don't want to do this.
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No, it is not cancer. Many places are now calling it a neoplasm of the breast instead of LCIS because the term is misleading.
Pet scans are for metastatic disease and LCIS is in situ, not invasive, so no, you would not get anything more than an MRI.
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Thanks Melissa.
I will not have an MRI again due to my COPD. I did it one time, but will not do it again, couldn't breath, it was extremely difficult.
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Those tables & the bar between your breasts are really rough.
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I totally agree with MelissaDallas. Almost everything about LCIS (including the name) is controversial.
Some oncologists consider LCIS as 'cancer', but probably most don't. That's because its hard to define cancer. Artists can draw pictures of cells that are clearly normal, and other pictures of cells that are clearly cancerous, but then there is this 'inbetween'. Many people in the public consider cancer as the ability to metastasize. LCIS and DCIS alone cannot metastasize. Both can probably, under certain circumstances, develop into an invasive cancer that can metastasize, or someone may have an invasive cancer at the same time as LCIS and/or DCIS which can metastasize. There isn't a sharp line between normal and cancerous. Cancer is usually called 'uncontrolled growth', but we can't study live LCIS under the microscope; we can only look at dead LCIS cells under the microscope.
LCIS is a strange disease, because its almost always an incidental finding. That means that its usually found when they find something suspicious in a mammogram (probably most commonly suspicious calcifications), and its suspicious enough to do a biopsy. They often call these suspicious areas things like 'lesions'. LCIS is often found not at these lesions, but adjacent to those lesions.
If an LCIS patient goes on and does get worse breast cancer (i.e. DCIS-which more people consider cancer than they do LCIS - or invasive breast cancer), the DCIS or invasive cancer is often at an area that previously looked totally normal.
So they don't know how all LCIS progresses. They do think that a) some LCIS does eventually become breast cancer (in other words, the LCIS is genetically related to the invasive breast cancer), b) most LCIS just stays in the breast and never becomes anything worse, and c) in other women who have LCIS and later get invasive breast cancer, thebbreast cancer is totally unrelated genetically to their LCIS.
I know there are several women here who have had immense trouble trying to stay perfectly still in very uncomfortable positions when they are getting imaging done. I'm so sorry you have had a rough time too.
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Thats the reason I opted for the excisional biopsy because I knew I couldn't lay on my stomach for an extended period of time for the stereotactic biopsy.
When I went to register for the stereotactic biopsy, they showed me exactly what I would have to do, and then asked me if I would be able to stay perfectly still and I said no, because I cough sometimes due to the COPD. She said she would not recommend this biopsy for me. I went back to the surgeon who did the lumpectomy instead.
When I went for the MRI, I told the tech I wasn't sure I would be able to complete the test. They gave me a panic button to use if I couldn't continue. I came very close to pushing that button...
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