Risk Assessment: Shouldn't ALL Tissues Count?
In risk assessment, we generally use wide excision tumor size and grade as primary metrics, correct?
Comments
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The final path report should incorporate results of all prior biopsies and breast surgeries for the final grade and size. Sometimes it is not possible to get a precise and accurate total size because they cannot reconstruct exactly how the tumor segments fit together, especially if the first surgical procedure was not expected to find cancer.
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I agree with redsox. One's final diagnosis should be based on a combination of what was found in all of the biopsies and surgeries.
A microinvasion of IDC was found in the pathology from my excisional biopsy. My final and more significant surgery, my MX, found only DCIS. However my final diagnosis was Stage I DCIS-Mi, thanks to that microinvasion that was found in the biospy.
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Just to agree with Beesie - I'm also Stage 1A due to the microinvasion that was found along with the small area of DCIS on my stereotactic biopsy, even though the lumpectomy found nothing (it was all removed by the biopsy).
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Thanks, ladies. How was it that you learned all this?
Is it standard pathology procedure to take into account a patient's previous paths, and render a report based on all info? -
There are standards for what should be included in the path report and how the specimen should be prepared. The standards depend on the diagnosis or expected diagnosis so they differ for a cancer diagnosis vs. an expected benign result. For cancer the final path report should incorporate all earlier findings.
I had a big head start when I was diagnosed because I have worked in cancer research for a long time. Some things I knew -- like the answer to your question because I knew we always look for the final path report. If it is done right that is the only one you need. -
Interesting. So, Redsox, how would you interpret final path on the following:
Biopsy: 5mm grade 2
Surgery: 6mm grade 1
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That looks like a report of each sample separately the biopsy info included in the final path report. Different sections of the tumor can have different grades so you have a combination of grade 1 and 2.
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I see. -And the size? 11 mm?
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The maximum tumor size would be 11 mm and that is how most doctors would describe it. It might be less depending on the relative orientation of the two specimens.
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Interesting. -Not sure that's how mine was done. I'll have to ask. I did make contact with Genomic Health, who did my oncotyping. For their purposes, they ask for one sample that is most representative of tumor genetics, as selected by one's local pathologist. In my case it was the surgery sample. I can't help but wonder if the biopsy sample wasn't more representative, especially if it was indeed of a slightly higher grade.
On second thought, why fuss with what was done in the past - my onc is not very available anyway. I've contacted Dr Lagios for his opinon. According to his literature, all samples are considered in his final path report. (A phone call confirms this.) He is directly available to patients and very affordable, in my opinion, for the quality of care. I'd like to see if he agress that the first sample is grade 2, then get his expert take on my omitting radiotherapy for now. -A little extra assurance can't hurt. (In case you'd like to know my story, here it is.)
Thank you, ladies (in particular Redsox) for your help. A great weekend to all! -
Update: Dr Lagios did downgrade my biopsy sample to low grade also, based on the absence of necrosis. He absolutely agrees that I should wait on radiotherapy, and advises that I omit Tamoxifen and other such drugs. After our 45-minute phone consult, I couldn't be more happy that I used his services, and couldn't recommend him more. If it is all right to post a link to his page, here it is. Thanks again for all your help, ladies.
Blessings and health to you,
Kay
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