What is high risk ??

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netrajkr
netrajkr Member Posts: 45

I'm 44 had a masectomy with 3 nodes removed the result was DCIS with 5 cm mass on June 24th..I had no family history of cancer .. I'm perfectly healthy neither over weight ..I have extremely dense breast and I never had children ?. My genetic tests were negative..My oncologist in its final note wrote that I'm at high risk ..

Am I ?? What should I do ?? I

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  • leaf
    leaf Member Posts: 8,188
    edited December 2015

    HIgh risk for invasive cancer? High risk for death from breast cancer?

    I think that the words 'high risk' are in the eyes of the beholder. Even assuming that you can accurately evaluate your risk (which I don't think you can very well- at least for you as an individual), how high is high?

    I've quoted this paper many time before. http://jnci.oxfordjournals.org/content/98/23/1673.... Its about the modified Gail model, which automatically excludes both you and me. Its meant to predict the average breast cancer risk of a group of women (without breast cancer) with certain risk factors. Unfortunately, its a really poor model for predicting the risk of any certain individual.

    I figure that if they know this little about predicting risk for an 'average' group of women without breast cancer, just think how well they know the risk of a person who has some risk factors?

    I know they know practically zip about LCIS, but I have seen or gotten lifetime risk predictions for breast cancer that range from 10% to 90% (the 90% in a non-peer reviewed calculator.) That's a pretty wide range. In ONE paper, in different places they described LCIS as a 'high risk' and a 'moderate risk' condition.

    I would imagine that having a mastectomy greatly reduces your risk, but there are always some breast cells left.

    Some doctors say things in notes in order to get insurance to pay for them. I have LCIS and sometimes my gyn described me as having breast cancer, even though almost no oncologists would (or should). (I was having a D+C for uterine polyps when I was taking tamoxifen.) Sometimes the people who are reviewing surgeries and treatments do not know all that much. I certainly remember an infectious disease specialist (MD of course), and he was challenged by the insurance company about an antibiotic treatment he recommended. The insurance company suggested a cheaper antibiotic. He pointed out that the antibiotic the insurance company was suggesting did not cover that particular bacteria!

    All this is very anxiety provoking, especially when you are newly diagnosed. But as you learn more, eventually most people come more to terms with their situation.

  • 614
    614 Member Posts: 851
    edited December 2015

    I would say that you may want to ask your MO questions until you are satisfied with the answers.  I am assuming that you have an MO.  If you do not,  then I would recommend finding one.  Your MO will monitor you on an ongoing basis which hopefully, will give you peace of mind. 

    I think that once anyone is diagnosed with bc that one is considered to be high risk, but again, this may be for insurance purposes as Leaf stated.

    Good luck.

  • inks
    inks Member Posts: 746
    edited December 2015

    Perhaps the oncologist considers you high risk because of ER/PR- and HER+ and your age? Or maybe he mentioned that because you will need ultrasounds on the remaining breast because of dense tissue? All you can do is to be vigilant about your follow ups and keep up your healthy lifestyle.

  • msphil
    msphil Member Posts: 1,536
    edited December 2015

    hello i had no family history of breast cancer was first in family was inly 42 yrs old healthy. So i dont believe they really know.msphil(idc stage2 0\3 nodes Lmast chemo before n after surgery rads 5yrs on tamoxifen)

  • msphil
    msphil Member Posts: 1,536
    edited December 2015

    oh n Praise God 21yr Survivor. msphil

  • LM070917
    LM070917 Member Posts: 323
    edited December 2015

    i would say that oncologists refine high risk (as in how advanced it is, how aggressive it is and how likely it is to recur) based on staging (how big the tumour is/was, whether nodes were involved and the chance of it spreading), the grade and whether is has any hormone receptors or not. I'm considered high risk purely because of my age (34yrs), tumour size, stage and grade, but we have the best treatment out there, then we have ever had, so don't get bogged down. I try to ignore the stats and get on with my second chance of life. Positive thinking is so important.

  • netrajkr
    netrajkr Member Posts: 45
    edited January 2016

    Thanks everyone ..It does calm my mind .reading all these thoughts ..

  • BLinthedesert
    BLinthedesert Member Posts: 678
    edited January 2016

    High risk of diagnosis typically refers to those who have not been diagnosed with a malignancy - and the risk that is being defined is "risk of being diagnosed with malignancy". That said, it can also be attributed to people who have been diagnosed, and treated, for breast cancer in the past, and in this case the risk is "risk of new breast cancer"

    Once you *have* been diagnosed with cancer, there is also the additional risk of "risk of recurrence, either advanced or local" that is directly attributable to prior diagnosis (typically a new lesion in the same breast or somehow attributable to prior diagnosis).

    It is typically assumed that all women with prior diagnosis of breast cancer are "high risk" irrespective of stage, grade, and other risk factors (such as those described in the Gail model). The Gail model is not used for women with prior breast cancer diagnoses for this very reason.


  • leaf
    leaf Member Posts: 8,188
    edited January 2016

    I think its very important to understand not only when a doc gives you a certain risk, but how well they know it. In the case of breast cancer, its NOT MUCH.

    But the Gail model has some limitations. It has predictive value only for women over age 35 who have not previously been diagnosed with breast cancer,67 and it does not incorporate specific genetic risk factors. Although it is highly accurate at predicting the aggregate number of women within various age or other risk groups who will develop breast cancer within 5 years, its ability to predict which individual women will develop breast cancer is only slightly better than chance.60 It is, nonetheless, used to assist in determining whether individual women should engage in cancer prevention measures, because there are no better models that have been validated for individual risk prediction. (emphasis mine). http://www.ncbi.nlm.nih.gov/books/NBK22312/

    Even different breast cancer risk model differ. In this paper, of 3 breast cancer risk models, Our analyses found that of the 5,894 women in this study, 342 (5.8%) were eligible for MRI by at least one of the models. There were large differences in the number of eligible women by each model. Most notably, the Tyrer-Cuzick model identified 330 (5.6%) of the study population to be eligible, whereas the BRCAPRO and Claus models identified many fewer eligible women (25, 0.4% and 54, 0.9%, respectively; Fig. 1). Surprisingly, only 13 women (0.2%) were identified to be eligible by all 3 risk models. When the BRCAPRO model results were adjusted to approximate the additional risk of DCIS, we found that these results changed slightly (Fig. 2). This adjustment identified more than twice as many women (61 women, 1% of the study population). Yet, the overlap between the models changed very little with only 18 individuals (0.3%) identified by all 3 models. (emphasis mine) http://cebp.aacrjournals.org/content/22/1/146.lo

    If they have this much trouble predicting the risk of women in the general population, just imagine the trouble they have in ONE woman who have some type/risk factor not included in the model.

    Even if you define 'high risk' as >X%, they sure don't know the value of X very much at all for any individual person.

    So if someone gives you figures about your risk of breast cancer, they sure don't know that number very well AT ALL.


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