Efficacy, safety, and biomarker analysis of neoadjuvant camrelizumab plus apatinib as a chemotherapy-free strategy for early-stage triple-negative breast cancer: a phase II study.

Breast Cancer Res TreatAug 31, 2026 (epub)
Clinical ResearchOncology (Medical)Open access

Zhenluan Tian, Hengyu Li, Yuxin Deng et al.

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In 30 seconds

This phase II clinical trial evaluated the efficacy and safety of neoadjuvant camrelizumab plus apatinib in patients with early-stage triple-negative breast cancer (TNBC) and high tumor-infiltrating lymphocytes (TILs). Among 11 patients who underwent surgery, the pathological complete response (pCR) rate was 27.3%, and the objective response rate (ORR) was 46.2%.

Key findings

  • The pathological complete response (pCR) rate was 27.3% (3/11) among patients who underwent surgery.
  • The objective response rate (ORR) was 46.2% (6/13) in evaluable patients.
  • The 24-month disease-free survival (DFS) rate was 90.9%.
  • Treatment-related adverse events (TRAEs) were mostly grade 1-2, with 28.6% experiencing grade ≥3 events.

Why it matters

This study presents a potential chemotherapy-free treatment option for early-stage TNBC, which may reduce toxicity while maintaining efficacy. Understanding the role of immune checkpoint inhibitors and anti-angiogenic agents could influence future treatment strategies.

Source

Published in Breast Cancer Res Treat. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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