Camrelizumab (PD-1) + chemo delivers 33% pCR in resectable stage III NSCLC, with ctDNA flagging relapse early
- Trial ID
- NCT06241807 on ClinicalTrials.gov
- Cancer type
- Non-Small Cell Lung Cancer (NSCLC)
- Published in
- New in Oncology - Aug 6, 2026
Camrelizumab is an anti–PD-1 monoclonal antibody given here with platinum-based chemotherapy as 3-cycle neoadjuvant chemoimmunotherapy in a single-arm Phase II study of resectable stage IIIA–IIIB NSCLC (n=30; 27 resected; 73% squamous), with pCR as the primary endpoint. pCR was 33.3% and MPR 50.0%; at median 27.2 months’ follow-up, 2-year DFS was 77.4%, with grade≥3 TRAEs in 13.3%—numerically in the same ballpark as perioperative PD-(L)1 + chemo benchmarks like neoadjuvant nivolumab+chemo in CheckMate 816 (pCR 24% vs 2.2% with chemo) and perioperative pembrolizumab+chemo in KEYNOTE-671 (improved EFS/OS vs chemo). Biomarker work linked pCR/DFS to higher baseline CD8+ and CD8+ naïve-like T cells (including spatial proximity in tumor nests), higher baseline circulating CCL3, and ctDNA kinetics; post-neoadjuvant ctDNA positivity predicted shorter DFS, and serial ctDNA detected relapse up to 17.6 months before radiographic progression (trial: NCT06241807).
Take home
If these biomarker signals hold up in larger, controlled cohorts, ctDNA (post-neoadjuvant “MRD” status) plus a baseline immune-readiness signature (CD8+ naïve-like density/spatial positioning, CCL3) could help decide who needs intensified perioperative therapy versus who might avoid overtreatment—especially important now that PD-(L)1 + chemo is already a high-performing (and increasingly crowded) standard in resectable stage II–III NSCLC.
Source: Read the original publication
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