Another Oncotype question
Comments
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Thanks to everyone again for your informative posts!
Txmomof 2: not sure if you're asking the range for Ki67 or if you meant oncotype.....I'm sure you'll get a quick answer if you clarify.
anndh: I'm sorry your score came back so high! Good luck with your chemo.
Quite frankly, I see more of a parallel between a low PR+ and the higher score......JMO
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mary71, I agree that a low PR+ will likely tip the scales to a higher oncotype score. I've understood that the degree of staining is of some importance and have wondered if it is taken into consideration on the oncotype. My ER and PR are lower than anndh's and Ki 67 higher, yet she had an oncotype score 4 pts higher than mine. My ER/PR were highly stained. I've not found this issue addressed in research papers trying to find a cheap way to approximate the oncotype score, probably because it is too difficult to get the data and very subjective.
Anyone else want to weigh in one this you your stats?
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mary71 - I was wondering if there was a low, mid and high range for ki67 numbers like there is for the oncotype score. I can't find anything about it.
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According to my pathology report, the range is as follows:
</10%: Low proliferation rate
>10% to </=20%: Moderate proliferation rate
>20%: High proliferation rate
Hope that answers your question :0)
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Thanks!
I always thought it was crazy that for the oncotype scale from 0-100, 0-18 is low etc. You would think 0-33 is low, 33-66 mid and 66-100 high. I guess it's the same thing for the ki67 scale.
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Otter - you're the only one who's ever been able to crack the code on what gene expressions they look at to compile the Oncotype score. I'm actually not surprised
I really liked your explanantion though. Much better than any I got.
Mary71, it's always a good idea to get input from here...as you said, they know what the real deal is. My own ER was 80% PR 95% onco was 50... but I was also HER+++ and my understanding is that usually equates to a higher score. I've also had one other cancer myself, and a family history of Liver cancer, so my score wasn't a surprise to me. I was glad to have it, as they initially wanted to only do hormonal treatment since I had a bmx. I didn't necessarily WANT to do chemo, but I'd hate to have needed it and not got it.
Best wishes on settling on a treatment plan, follow your gut, sometimes it's your best guide.
Navy
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My PR results via IHC staining were negative...0%. However, Oncotype came back as highly PR+. (I was highly ER+ on both tests.) Overall Oncotype score of 16, with 4 MOs saying that I could *not* do chemo!
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So my oncotype score is in.....16. Don't know if my high ER + had anything to do with it being low but no chemo for me. I'll see my MO on Tuesday for all the details of my oncotype dx.
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Navygirl, you seem to be the only one I see with a oncotype score as high as me; 51. I am ER+/PR+ but don't know the numbers on how high those were and I need to ask about the Ki test everyone here is mentioning. After an initial diagnosis of DCIS (cancer "lite") and having a lumpectomy, the bottom fell out. The BS surgeon found 2 tumors that had not shown up on any mammo; both were IDC with positive margins. Going back for a mastectomy on the 9th and they will do sentinal lymph nodes at that surgery. (nothing to indicate a need the first go round) I will be having chemo; the onco is waiting till lymph node info before deciding on what and how long, but she did say it will be a long round (due to the high oncotype)
Hope I'm making sense. You all are SO much more knowledgable than I am. I appreciate all the info I get here. Thank you all.
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Vicki - You're Her2+ and that is probably why your oncotype is so high.....that makes sense. I'm surprised they even ordered an oncotype?
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wildrumara, my test results have everyone scratching their heads, so I think my onco was just wanting to verify and have as much info as possible. One of the tumors was HER2+ and the other was HER2-. Combined with positive margins But well-differentiated margins, my onco, BS and the pathologist are all scratching their heads.
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I guess this thread is in a resting phase? Too bad, I was hoping someone would be able to translate my oncotype of 51 into a percent? I see many of you giving a score then corrosponding percent and I have no idea how to get that. Have an appt with my Med Onco on Monday to discuss the still puzzling results of my path report from the mastectomy. In most other situations, I would find it funny that I have doc's scratching their heads, but in this case, not so much.
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vickilind61--When you meet with your MO, they will go over the oncotype score with you. Included in your report is a graph reflecting your % chance of distant recurrance based on chemo or no chemo. Hope this helps.
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I had higher PR than ER. but ER was still moderate...it is actually GOOD news to have a higher PR because I read in some pubmed publications, there's a lower mets with that. But with cancer, there are NO 100% anything. Just stats and probabilities. Each one of carries our own monster as latest research says there's 40 genes involved in initating breast cancer!!!!
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Thank you Mary; I know I came in at about 38% chance of recurrance, which my MO said will be cut by about 1/3 with my treatments. Pretty high but still, it is what it is.
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Bluepearl - my UCLA MO said that a high PR was a good thing to have as it indicated a less aggressive cancer. So, it seems like what we want for a low Oncotype score is ER and PR as high as possible and KI67 and grade as low as possible. My MO claims to be able to predict Oncotype scores (low, intermediate or high at least) with just these four factors. I would think HER2+ would automatically give a higher score but we didn't discuss that since I'm HER2-.
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I was not really expecting chemo, since I had a dmx, one little 8mm tumor, no nodes. But i was grade 3, maybe 30% ER pos (Will check!) and oncotype 38. KI67 43. So I am about to have #3 of my TC4. I so wish I could have just recovered from surgery and had that be it plus maybe aromatase or whatever. Sigh.
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Not sure what the test is and what it shows. I was not given it for some reason---
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lisa - my oncotype score is close to yours, 39, Ki67 60%. I am ER (9.0, 90%) PR(5.7,5%) Her2 neg...first score from onco, second from initial path. They definitely threw the chemo book at me.
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Dogsandjogs: I don't think they automatically give the oncotype if the Mo and you agree on the treatment plan. My first MO said no chemo or Herceptin due to the small size and wouldn't order an oncotype because I am HER2+!
This didn't sit well with me so I have a new oncologist who agreed that an oncotype would be called for. I get to review it with some other test results tomorrow. Even if the treatment plan is the same....I feel more confident in getting as much info as possible. And all the ladies on this site have encouraged me to be more assertive in my care plan! Thank you ladies! -
Yeah. My MO asked if I had made up my mind that I "wanted to throw everything at this" by having chemo, or if I was dead set against it. He said in either of those cases it made no sense to do the test. If I was willing to consider all my options we'd do the test. So we did, and I came back with a 9, so no chemo.
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Here's a head scratcher: my ER was around 30%, my PR neg
( don't know %, will ask Weds) . However, on my oncotype it said ER neg. now, the onco is really only for ER pos, right? My dOc said he'd never seen that discrepancy before. Could be diff cutoffs but weird. The chemo was what he thought was best anyway but want to understand more about this. -
Chachamon: When I got my diagnosis after the core biopsy, the onc told me no chemo would be necessary. He didn't bring up oncotype and I never knew the word until I saw it on this web site. I couldn't continue with the original onc because he didn't accept United Healthcare so I had to go to another onc for the follow up after surgery. Again, the name: oncotype was never mentioned. Odd, isn't it?
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Not so strange Dogs&j, I suspect that many of them don't suggest the test if they feel certain of the direction they want to go. It's a very expensive test, in the neighborhood of $4500. In my case the pathology of the tumor seemed to say chemo wasn't warranted, but the size of the primary tumor, and the fact that it had a couple of evil little friends meant that MO would have recommended chemo out of an abundance of caution (pre OncDx) so after agreeing that I didn't have strong feelings one way or the other (who me? I was so confused I wanted someone to give me THE answer) we went for the test. Test was done in March and I believe my insurance is still denying and being appealed for payment.
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Dogsandjogs: I agree that it is " odd" from a patient's perspective....but as Cindy said....it is a very expensive test. I was prepared to get a third opinion outside Kaiser, thinking it was perhaps an insurance cost issue, but my 2nd MO (the only woman oncologist in my network) didn't hesitate to have it ordered.
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I had to ask for it 3 times. MO said it wouldn't change his mind. Oh.....I thought I was the one to decide chemo or not. It came back 4, so I decided against chemo. I would have done chemo for an intermediate or high score. My MO thought I should decide just on the reoccurence pecentages from Adjuvant online he gave me. He said I needed to decide which risk to take, chemo or no chemo.
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Mary, you might want to look at a couple of the other threads regarding the OncotypeDX score on the Stage l and ll forum. Look especially for otter's contributions. Also read the OncotypeDX pages on this site for more information.
The OncotypeDX is a 21 gene test, which explains, at least to me, a non-scientist, why there seems to be no relationship between ER, PR, and HER2/neu status, .
I'm also waiting for the results of the test, due back June 7 to 11, I judge, because of the holiday.
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HealingDreams--Thank you for that. I received my oncotype score and based on that and many other things, I decided to begin chemo. Personally, I would rather be overtreated than undertreated. Good luck to you :0)
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Hi, ladies! My MO told me today that my score was 20 "low to intermediate" and that chemo posed more risk than benefit in my case....so I'm not doing the chemo and will be on Tamoxifen for 1 1/2 years and then switch to an aromatase for the last 3 1/2 years. Fingers crossed!
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Chachamom, that is great! Enjoy the no chemo, but you might want to check out the bottle of tamoxifan thread; lots of great info there.
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