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New Drugs Are Replacing Chemo for Aggressive Breast Cancer
The FDA has approved Trodelvy and Datroway as first-line treatments for triple-negative breast cancer. These antibody-drug conjugates target specific proteins to deliver chemotherapy directly to tumor cells. Both drugs reduced the risk of disease progression by about 40% compared to standard chemotherapy.
What changed
Gilead's Trodelvy received FDA approval for first-line triple-negative breast cancer treatment.
Live updates
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FDA Approves New Targeted Therapies for Aggressive Breast Cancer
confidence 100%The FDA has approved Trodelvy and Datroway as first-line treatments for triple-negative breast cancer. These antibody-drug conjugates target specific proteins to deliver chemotherapy directly to tumor cells. Both drugs reduced the risk of disease progression by about 40% compared to standard chemotherapy.
What's confirmed:
- The FDA approved Trodelvy for first-line triple-negative breast cancer.
- Trodelvy can be used alone or in combination with Keytruda for first-line triple-negative breast cancer.
- Datroway, developed by AstraZeneca and Daiichi Sankyo, was approved for a similar group of patients in May.
- Trodelvy and Datroway reduced the risk of disease progression by about 40% compared with standard chemotherapy.
- Both Trodelvy and Datroway are antibody-drug conjugates that target proteins on triple-negative tumor cells.
- The FDA approved IBRANCE in combination with trastuzumab, with or without pertuzumab, and endocrine therapy for maintenance treatment of adult patients with HR+ and HER2+ locally advanced or metastatic breast cancer.
Still unconfirmed:
- European regulators are expected to provide a verdict on Trodelvy's new indication later this year.
- Upward of 48,000 Americans were diagnosed with triple-negative breast cancer last year.