Anyone who was Stage 1 Grade 2 who did not do chemo?
Comments
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@dtad - That is interesting. Do you have links to any of the articles?
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yesterday, the physician / researchers released a prospective study with respect to the OncotypeDX test! It is called TailorX....
What it confirmed was it is an excellent determinant as to whether or not chemo is necessary BASED ON GENETIC MAKE/UP. While we are waiting for additional results from the study, probably in late 2017.... In the meantime we have an accurate test for a subgroup of patients that trumps traditional pathology examination
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dyad and 39andhip: I've read that as well. It was awhile back and I'm not sure if I still have the articles bookmarked, but I'll take a look.
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I've read that as well. It was something about the mitotic index- that is, if the other two categories (tubules and nuclear) are 3s and mitotitic index is 1 for a total of 7, that could be a lab error- something to do with formalin fixation time- and the tumor is more likely to be a grade 3, not a grade 2.
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This whole journey with breast cancer has been tough. Now to hear that there is no Grade 2....just Grade 1 and 3....makes it really hard to handle for me, because it means that my cancer is no longer considered moderate....now it's Grade 3 which makes it aggressive.
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I am post four weeks with mastectomy. I am stage one with no node involvement. I'm waiting for my onco results. I am on arimidex and will undergo radiation in about a week. The radiation is my choice. It is hard for anyone to tell you what to do. I've chosen not to do chemo. Good luc
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I am three years out, stage 1C tumor, grade 2, oncotype 19, IDC in R breast and DCIS in L. Only able to tolerate Tamoxifen for 10 months, no chemo. Still NDE.
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I am two years from Mx, also stage 1C tumor, grade 2, Oncotype 11. No chemo was recommended. I started on Arimidex and had side effects and MO switched me to Tamoxifen after 1 year (which I have been on for a year now with fewer side effects.)
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gammyyet.
Just curious. If you choose not to have chemo why get oncotype?
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My doctor ordered my oncodx my insurance paid, but I knew I would not do chemo based off the statistics too many variables.
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i refused six months fec chemo had three weeks radiotherapy then on arimidex then exemerstane then letrozole i was told the chemo was a kind of insurance policy and advised strongly to take it however i decided against it i went through hell on the tablets hence the three different ones ive now been discharged and put on another five years of tamoxifen ten days ago im having strange heads still in pain and taking deep breaths like panic attacks if these don't subside in back to see my gp next week it was Sept 2010 when I had my op lumpectomy and sentinel nodes two were attacked so a month later had full node clearance still in pain from tablets and trigger finger from letrozole but keep plodding through im now 72 years old i love gardening so this keeps me going l. regards Sandy
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I was recommended to do chemo by my MO, however (everyone has their own unique situation to guide them) I am considering opting out because the potential risks in my particular case (I have other health issues) don't seem worth the benefits. That being said, my BS wants to talk to me tomorrow about it. I would love to hear from other folks who decided to opt out and why
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I was stage 1 grade 2, ER/PR+, Her2+. Oncotype score was 19, so I was on the very grey border but chose chemo just so I could have peace of mind that I did everything I could. It was 4 rounds of TC. Ovaries were removed September 2015, and I had had a hysterectomy 7 or 8 years ago due to a large fibroid.
Was only able to make it through 2 rounds of chemo due to whole body hives and almost daily migraines, but the onco thought I did get some benefit from it and was OK with me stopping.
Now I just take Arimidex. NED yet, and although it's only been a year, I expect it to stay that way since I had a double mx. -
I am Stage 1, Grade 2, with an Oncotype score of 27.
I refused chemo. My MO suggested chemo based on my age, (41), but could not tell me if the benefits to chemo outweigh the risks. I am node negative and received clean margins during my lumpectomy. I just couldn't put my body through chemo without knowing for sure, that I would receive some benefit of it.
I now have 3 more radiation treatments left and then will go back to see my MO, to get on Tamoxifen.
While I'll always be nervous about a recurrence, I feel like I made the best decision for me. I know of women who had a recurrence after doing chemo and I know of women who had a recurrence without doing chemo. I truly believe that so much of this is a total crap shoot.
I will do everything that I can to be and stay healthy.....eat well, exercise daily, enjoy life, etc. If the cancer comes back, it comes back. Honestly, there is not much I can do about that except to deal with it if it happens. (Easier said than done sometimes!) -
My MO and NP told me that grading a tumor was subjective and decided on by the pathologist looking at the slide. As an example, on biopsy I was a grade 3 but after lumpectomy, another pathologist deemed me grade 2. I would go more on the oncotype score, although I wasn't given the test because I was Her2+++ so it was pointless.
So my message is, don't read too much into the grading system and trust your MO.
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I couldn't do the chemo either, my oncodx was 34. I was 53 at dx and so far so good. We shouldn't have to make hard health choices. I know some people sail thru chemo with no permanent side effects, but I just didn't think it was best for me.
After 4 years I think I am done with AIs.
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My ultrasound-guided biopsy said 7-9mm, IDC grade 2, ER+/PR+/HER2- Surgeon preliminarily staged me IA, pending nodes & margins, of course. I asked her NP at the pre-op teaching session about OncotypeDX, but she said they could only do it on surgically excised, not core-biopsy, tumor tissue; that most women clearly won't need it (because they obviously will or won’t be chemo candidates)--so because of the expense they save it for only those in the “gray area." (Wouldn't elaborate as to what constitutes “gray area").
Surgical path report confirmed IDC grade 2 (nuclear 2, tubule 3, mitotic rate 1), highly ER/PR+ and HER2- (+1, which was considered “negative" rather than “equivocal"). Clean margins, 4 nodes (2 sentinel, 2 hitchhikers) removed, all negative. BUT the tumor size was 1.3mm. Still Stage IA, but tumor size was now t1c. Hello, “gray area." Told my MO I didn't want chemo because of other comorbidities, and she said she'd be very surprised if the OncotypeDX came back high enough to recommend it. Score came back 16, at the higher end of “low"--and she showed me the graphs that indicated that at almost age 65, my chance of 10-yr recurrence was 8% on an AI+radiation alone, but adding chemo would bring it down to only 7%--the risks of chemo outweighed any potential benefit in my case. Acc. to the AdjuvantOnline tool, chemo would give me only an extra year of life....with no guarantee as to the quality of that extra year.
Mind you, had I been 44 or even 54 when diagnosed, I might have considered chemo. But bearing in mind that chemo kills only rapidly-dividing cells (malignant or normal), and my cancer, a Luminal A type, was slower-growing and probably wouldn't really respond to chemo, I might have been persuaded even then to have forgone it.
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Chisandy, also those numbers are with tamoxifen they are finding AIS are even more effective. I think you made the right decision I had the same break out as you on the grade.
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Hello,
I am curious about the same thing as I am leaning towards NO CHEMO as well. I am a Stage 1 but not sure of my Grade. Have you had many responses? I am new to the site and I'm learning how to navigate it but I have not yet figured out how to see responses to posts.
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Hi, KPittman! I'm sorry for the duplicate response here (I also posted this elsewhere on the site): I am also stage 1 (grade 3), however, after the MammaPrint result came in, two MOs and my BS suggested I do 12 weeks of chemo. I opted not to do it because of negative nodes and other health issues. For me, it wasn't worth the potential risks involved. If you are unsure what to do, don't hesitate to seek out another opinion. Also, you may want to request a copy of your pathology report and copies of your various scans. Your tumor grade should appear on your pathology report.
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stage 1, grade 2, oncotype 19 and chemo was not recommended
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What's the cut off for "young?" I don't consider myself that young, but then not old either ;-). I was 50 at diagnosis, 51 at surgery (day after my birthday). Tumor was 1.5mm, mitotic rate 1, ki-67 4%, nuclear grade 3, tubular grade 2, overall grade 2 (read on another thread that grade 2's should really be classified as grade 3?!). Oncotype 17. Three doctors said no chemo, just Tamoxifen for a few years, then switch to AIs when confirmed post-menopausal.
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I read generally that between Grades 2 & 3, the most important factor is degree of differentiation from surrounding normal cells, followed by mitotic rate. Tubule score was not as important. Mine was tubule score 3 (the higher the proportion of tubules to overall tumor cells, the
lowerthe tubule score and thus the better), mitotic rate 1 (slowest-dividing) and “moderately differentiated” (i.e., moderately different-looking from surrounding normal cells), adding up to Grade 2. Grade 1 is “well-differentiated” (very different-looking from and fewer than surrounding normal cells) and Grade 3 “poorly differentiated” (nearly identical to surrounding cells which are also not “normal” looking). So I don’t see how Grade 2 should be relabeled Grade 3--there really is a middle ground. Most Luminal A tumors are Grades 1 or 2. -
Hi KPittman.
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Best of luck,-----hope the above is clearer than it looks on re-reading it!!!!!!
GP
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ChiSandy - you seem to know so very much about the details of BC - your posts are extremely helpful. Perhaps you can answer a questions for me. In post-menopausal women, it a high ER% better in terms of anti-hormone treatment? My initial biopsy showed 100% ER+ with strong staining which indicated to me that my ILC was VERY driven by Estrogen. Does it stand to reason, then, that any remaining cells will be VERY responsive to AI (or Tamoxifen)?
Your thoughts?
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my score was 25, I opted for Chemo. .. I am taking the hormone blockers for 10 years. I am in a group and see lots of METS. Since you can't go back I would make sure I took the hormone blocker for 10 years or what ever your doctor advises. but i would not do any less since that is the only line of defense you have at this point
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I had colliad Mucous carcinoma only 5% present of women have this it is rare. I was stage 1 grade2, no lymph node involvement , no chemo, had radiation thru a Savi, all clear margins after lumpectomy after everything was over I was put on Hormone Receptor. This was in Aug. 2015, 8 months later came back in same breast on the opposite side, going back in for surgery 5/25 this year, This time it is under a vessel my biopsy is undertermin they don't know what it is just stated it should be removed.
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Dear Margiep, Welcome to the community. We are sorry about your diagnoses but glad that you reached out here. Stay connected. Keep us posted and let us know if we can help you navigate the boards. The Mods
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I was stage IB, grade 2
I was diagnosed at 27, in 1999 and they didn't have the Oncotype scoring then.
I didn't do chemo (my oncologist and 'tumor board' didn't feel I needed it) just lumpectomy, node dissection, radiation, and 2.5 years of Tamoxifen.
I'm 16 years out
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Tmh0921 - ALWAYS good to hear from someone as far post-BC as you (16 years). Thanks for chiming in and letting us know - inspiring for all us newbies.
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