Exciting breast cancer news More women can safely forgo chemotherapy
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Data from a 2018 study have confirmed the standard of care for many women with early-stage breast cancer: chemotherapy isn’t always necessary, and actually is unlikely to be effective in certain women This is incredible news because more women potentially can avoid the toxicity of chemotherapy as well as the financial and time burden of chemotherapy treatments.

The new study published in The New England Journal of Medicine, revealed that a majority of women over 50 who have estrogen receptor-positive and lymph-node negative breast cancer don’t benefit from chemotherapy. This is the largest prospective study ever conducted in terms of breast cancer treatment, and the findings have the potential to impact treatment decisions of up to 70,000 patients a year in the United States.

The results validate the standard of care for breast cancer patients that we have provided at MedStar Washington Hospital Center for over a decade. All our patients receive personalized care, including the use of genomic tests such as was done in this study to make recommendations on whether individual women might benefit from chemotherapy. The study focused on cases in which chemotherapy’s value to women with breast cancer was already in doubt as a standard of care, including cancers that are:

  • Hormone receptor-positive, or grow due to estrogen or progesterone
  • In the early-stage and have not spread to lymph nodes
  • Not the type that the requires use of targeted drugs such as Herceptin
A study from @NEJM suggests that chemotherapy is not always necessary for women with intermediate-risk, early-stage breast cancer. bit.ly/2MjqfPr via @MedStarWHC
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What the data say

Researchers in the study examined the results of more than 10,000 women with breast cancer who had a test called Oncotype DX. The test is performed on their tumor to estimate the risk of recurrence through measuring the activity of several cancer genes involved in cell growth and their response to hormone therapy (a cancer treatment that limits the growth of cancer causing hormones) and chemotherapy. Women were only included in the study that had estrogen receptor positive (ER+) tumors, tumors that were negative for human epidermal growth factor receptor (HER2) over expression, and had negative lymph nodes.

Approximately 17 percent of women who met criteria for this study had high-risk scores and were advised to undergo chemotherapy. Approximately 16 percent of women had low-risk scores and were recommended to only receive hormonal therapy.

The results focused on the remaining 67 percent of women who were considered at intermediate risk. All these women had breast cancer surgery and hormone therapy, and half also got chemotherapy. After nine years, 94 percent of the patients from both groups were still alive, and about 84 percent of the survivors had no signs of cancer, which suggests that chemotherapy made no difference in their types of cancer.

What’s next for chemotherapy?

Even before this study, breast cancer treatment standards had been moving away from chemotherapy for select patients. As more advanced and personalized treatment options have become available, chemotherapy recommendations are made less often. Moreover, I expect as more targeted therapies and immunotherapies are scientifically studied and become available, less chemotherapy (and associated toxicity) will be needed.

At MedStar Washington Hospital Center, we routinely use genomic tests such as Oncotype Dx to identify patients who are at low or intermediate risk of breast cancer recurrence and are not likely to benefit from chemotherapy. However, we know that women at high-risk of breast cancer recurrence who have breast cancer that is triple-negative, HER2-positive, or lymph-node positive can benefit from chemotherapy.

This research will help validate treatment decisions for more women and their doctors. The next step in research will be extended, longer-term follow-up of breast cancer patients. Taking it a step further, we may improve genomic assays to determine whether there is a better line in the sand at which we can feel 100 percent confident that a woman doesn’t need chemotherapy. I don’t know when we’ll ever get there, but I do think there will be improvements in the near future. In the short-term, I believe we’ll see women with breast cancer and their doctors feel more comfortable using genomic tests to make decisions about chemotherapy.

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