Pembrolizumab (PD-1) cuts MCC-specific relapse events in resected Merkel cell carcinoma, with signal for better distant control
- Trial ID
- NCT03712605 on ClinicalTrials.gov
- Cancer type
- Merkel Cell Carcinoma (skin)
- Published in
- New in Oncology - July 16, 2026
Pembrolizumab is an anti–PD-1 checkpoint inhibitor tested as adjuvant therapy in the randomized Phase III STAMP trial (EA6174; NCT03712605) after complete resection of stage I (no SLNB) to IIIB Merkel cell carcinoma: pembro 200 mg IV q3w ×17 (n=147) vs SOC (observation and/or protocol-directed RT as planned) (n=146; median follow-up 47 months, data cutoff 2/19/26). The co-primary RFS endpoint defined as recurrence or death from any cause (RFS_a) was numerically better but not statistically significant (one-sided p=0.10), while MCC-specific RFS (RFS_b) improved with HR 0.66 (90%CI 0.45–0.96; one-sided p=0.032) with 1-year/2-year RFS_b 84%/77% vs 73%/67% on SOC; DMFS also improved (one-sided p=0.05). By design, SOC in this setting is typically surveillance with selective adjuvant radiation rather than routine systemic therapy—RT improves local/regional control in historical series but does not reliably prevent distant relapse, which is where this pembro signal is most relevant.
Take home
If the field accepts MCC-specific RFS as the more “on-target” endpoint here, STAMP suggests adjuvant pembrolizumab may finally move the needle on distant relapse risk after surgery—especially when RT is delivered sequentially (not concurrently)—but the lack of a clear all-cause RFS win means OS/mature survival and a clean RT-timing story will matter for practice change.
Source: Read the original publication
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