Question about Oncotype Test
So, i got my ocnotype test score of 10. i'm happy with it. but then i got to looking at the ACTUAL test, and the score is based on taking tamoxifen for 5 years. well, i'm "over the hill" and in menopause, so im NOT doing tamoxifen, i'll be doing one of the other AI's.
does the result of the test translate the same? i didn't see that part before i left the mo's office, so didn't have a chance to ask him. i also think i peeved him off a bit when he told me i'd be cured. i muttered to him that 10% chance of recurrence wasn't a cure. it seemed like he took that personally. oh well, he didn't just loose his boob, and i did.
anyhoo- does anyone know about this? and if not, whom might i ask that won't tell me to just "can" it, and stop worrying......
Comments
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I believe AIs are even more more effective than Tamoxifen regarding reducing recurrence risk.
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Someone can correct me if I'm wrong but I think the statistics would be the same for AI use.
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^ where's the "like" button?
thanks, MelissaDallas!
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I asked my MO this exact question as I opted to go with ovarian suppression and AI as opposed to Tamoxifen due to slightly better track record and he said the Oncotype score good with any anti hormonal. I took his word for it. 15 days on AI and so far so good.
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I saw one preliminary study that showed a marked decrease almost halfing the risk score in the group where er+ and pr-, or luminal b when AI used instead of tamoxifen.
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Hi Dodes:
The Oncotype Reports currently feature the results of early validation studies in which patients were assigned to receive either: (a) 5 years of Tamoxifen Alone; OR (b) Chemotherapy plus 5 years of Tamoxifen. Therefore, the information about recurrence risk in the current Reports reflects risk with a specific endocrine therapy (Tamoxifen). However, in light of other clinical evidence, in practice, patients receiving the test will receive a case-specific recommendation for endocrine therapy that is appropriate to their particular situation (e.g., Tamoxifen, an Aromatase Inhibitor).
Here is an example of a later Oncotype validation study conducted in patients who had received 5-years of the aromatase inhibitor Anastrozole. This study used samples and 9-yr recurrence rates from the tamoxifen arm and the anastrozole arms of the ATAC trial, in node-negative and node-positive postmenopausal women with localized breast cancer.
>> "Prediction of Risk of Distant Recurrence Using the 21-Gene Recurrence Score in Node-Negative and Node-Positive Postmenopausal Patients With Breast Cancer Treated With Anastrozole or Tamoxifen: A TransATAC Study"
>> Dowsett (2010): http://jco.ascopubs.org/content/28/11/1829.full.pdf
Those who are node-negative ("pN0") with a Recurrence Score of 0 to 10 may also be interested in the results of the prospective TAILORx trial. This trial was conducted in patients with node-negative (N0), hormone receptor-positive, HER2-negative disease and (consistent with current clinical practice) permits a variety of endocrine therapies. The 5-year results for those with Recurrence Scores of 0 to 10 assigned to receive endocrine therapy alone were reported here:
>> "Prospective Validation of a 21-Gene Expression Assay in Breast Cancer"
>> Sparano (2015): http://www.nejm.org/doi/full/10.1056/NEJMoa1510764#t=article
>>QUOTE: "In the low-risk cohort of 1626 patients [with Recurrence Scores of 0 to 10], endocrine therapy included an aromatase inhibitor in 963 patients (59%), tamoxifen in 560 (34%), sequential tamoxifen followed by aromatase-inhibitor therapy in 13 (1%), ovarian-function suppression in 44 (3%), or other or unknown therapy in 46 (3%)."
BarredOwl
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Dodes,
Do that happy dance
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