Treatment for Early Stage Triple-Negative Breast Cancer

Different chemotherapy drugs are used to treat triple-negative breast cancer and they are often used in combination with one another. "Patients may see names like ACT, TC or CMF, but those just stand for the regimens that we use," says Dr. Comen.

For example, a CMF regimen is an abbreviation for the combination of chemotherapy drugs cyclophosphamide, methotrexate, and fluorouracil. AC stands for doxorubicin (Adriamycin) with cyclophosphamide, and ACT just indicates that a taxane drug is added to the regimen. Likewise, TC is an abbreviation for a regimen consisting of Taxotere and cyclophosphamide.

Be sure to talk to your doctor, assess where you are in your diagnosis, and work through what the best options are for you.

Immunotherapy Recently Approved

In 2021, the FDA approved the immunotherapy drug pembrolizumab for the treatment of early-stage triple-negative breast cancer (TNBC). Pembrolizumab (Keytruda) is already used to treat other cancers, including melanoma and non-small cell lung cancer. Doctors heralded the FDA's approval of pembrolizumab as a potentially paradigm-shifting advancement in breast cancer treatment.

For patients with stage 2 or 3 TNBC, adding the immune-boosting medication pembrolizumab to combination chemotherapy before surgery, increases chances of living free of breast cancer, explains oncologist Dr. Sylvia Adams, director of the Breast Cancer Center at NYU Langone's Perlmutter Cancer Center. She was one of several researchers involved with the pembrolizumab trials. "It changes the standard of care and should be discussed with all patients who are diagnosed with stage 2-3 TNBC," she adds. "Yes, it's a game-changer, though there is much more to be learned."

In the phase III trial that preceded the FDA's approval, a regimen of pembrolizumab with neoadjuvant (before surgery) platinum-based chemotherapy and then pembrolizumab alone extended event-free survival in patients with early-stage TNBC. The trial included 1,174, with 784 receiving 200 mg of pembrolizumab every three weeks in addition to neoadjuvant chemotherapyfour cycles of paclitaxel and carboplatin and then four cycles of doxorubicin or epirubicin plus cyclophosphamide. The other 390 study participants received chemotherapy plus placebo.

At the median follow-up of 39 months, pembrolizumab showed a significant event-free survival benefit compared with chemotherapy alone. All patients underwent surgery and received radiation therapy as indicated. Adjuvant treatment (after surgery) included up to nine cycles of pembrolizumab or placebo, depending on which randomized group the patient belonged. The number of cycles varied depending on factors such as disease recurrence or unacceptable toxicity. Pembrolizumab is an anti-PD-1 monoclonal antibody administered intravenously.

 

 

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