Effectiveness and safety of cemiplimab in locally advanced and metastatic cutaneous squamous cell carcinoma.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
83 patients with lacSCC (n = 53) and mcSCC (n = 30).
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Head&neck tumor site was associated with a longer OS after first progression (OS2, HR 0.29, 95% CI 0.09-0.89). This study supports the safe and effective use of cemiplimab in real life clinical practice yet highlights the need for further identification of new predictors of clinical response.
Cutaneous squamous cell carcinoma (cSCC) is a common skin cancer with increasing incidence.
- 표본수 (n) 53
- p-value p = 0.002
- p-value p = 0.003
- 95% CI 9-55
APA
Roccuzzo G, Bongiovanni E, et al. (2026). Effectiveness and safety of cemiplimab in locally advanced and metastatic cutaneous squamous cell carcinoma.. Frontiers in pharmacology, 17, 1601650. https://doi.org/10.3389/fphar.2026.1601650
MLA
Roccuzzo G, et al.. "Effectiveness and safety of cemiplimab in locally advanced and metastatic cutaneous squamous cell carcinoma.." Frontiers in pharmacology, vol. 17, 2026, pp. 1601650.
PMID
41868132 ↗
Abstract 한글 요약
Cutaneous squamous cell carcinoma (cSCC) is a common skin cancer with increasing incidence. The anti-PD-1 therapy cemiplimab has shown its antitumor activity in locally advanced (lacSCC) and metastatic cSCC (mcSCC). This retrospective study assessed the real-life effectiveness and safety of cemiplimab in 83 patients with lacSCC (n = 53) and mcSCC (n = 30). The objective response rate (ORR) was 49.4%, with a complete response (CR) in 15.7% and a partial response (PR) in 33.7%. The median progression-free survival (PFS) was 14 months (95% CI 9-55) and the median overall survival (OS) 19 months (95% CI 10-39). Half of patients (50.6%) experienced adverse events (AE) of any grade, with 8.4% discontinuing therapy due to the severe AEs. The subset of patients who experienced progression during therapy displayed younger age (p = 0.002), a higher disease stage at baseline (p = 0.003), and a nodal disease (p = 0.041). No differences in survival outcome emerged between patients with nodal vs. distant metastases, previous radiotherapy recipient vs. radiotherapy-naïve, and immunosuppressed vs. immunocompetent patients. Head&neck tumor site was associated with a longer OS after first progression (OS2, HR 0.29, 95% CI 0.09-0.89). This study supports the safe and effective use of cemiplimab in real life clinical practice yet highlights the need for further identification of new predictors of clinical response.
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