Pembrolizumab plus chemotherapy improved event-free survival in Japanese patients with untreated locally advanced triple-negative breast cancer
This phase 3 randomized controlled trial subgroup analysis evaluated the efficacy and safety of neoadjuvant pembrolizumab plus chemotherapy followed by adjuvant pembrolizumab in 76 Japanese participants aged ≥18 years with previously untreated locally advanced triple-negative breast cancer (stage T1c N1-2 or T2-4 N0-2). Participants were randomized to receive pembrolizumab 200 mg plus chemotherapy every 3 weeks for 8 cycles, followed by surgery and adjuvant pembrolizumab for up to 9 cycles, or placebo plus chemotherapy on the same schedule. The median follow-up was 76.3 months as of March 22, 2024.
The primary outcomes were pathologic complete response (pCR; ypT0/Tis ypN0) and event-free survival (EFS). The pCR rate was 24 of 45 (53%) in the pembrolizumab group versus 15 of 31 (48%) in the placebo group (difference 4.9%, 95% CI -17.6% to 27.1%). EFS at 60 months was 84% in the pembrolizumab arm versus 73% in the placebo arm (HR 0.54, 95% CI 0.20–1.50).
Grade 3 or 4 treatment-related adverse events occurred in 37 of 45 (82%) pembrolizumab-treated participants and 23 of 30 (77%) placebo-treated participants. No grade 5 treatment-related adverse events were reported. Safety was considered manageable. Limitations include small sample size and lack of reported data on discontinuations and absolute numbers for EFS. Findings support the use of pembrolizumab with chemotherapy in Japanese patients with high-risk early-stage TNBC, though results should be interpreted with caution due to wide confidence intervals.