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EU Approves T-DXd for Residual HER2-Positive Early Breast Cancer

Original: T-DXd Gains EU Approval in Residual HER2+ Early Breast Cancer

The European Union has approved trastuzumab deruxtecan (T-DXd) for patients with residual HER2-positive early breast cancer, expanding access to the antibody-drug conjugate beyond its existing metastatic indications. The decision follows positive trial results showing improved outcomes for patients with remaining disease after neoadjuvant therapy. Oncologists have welcomed the approval as a meaningful new treatment option in the curative-intent setting.

Why now: The EU's regulatory approval of a major oncology drug in a new early-stage setting is fresh news of direct relevance to cancer patients and clinicians.

T-DXdEuropean UnionDaiichi SankyoAstraZenecaHER2-positive breast cancer

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