Phase II Study of Pembrolizumab As First-Line, Single-Drug Therapy for Patients With Unresectable Cutaneous Squamous Cell Carcinomas

E. Maubec(Université Sorbonne Paris Nord), Marouane Boubaya(Assistance Publique – Hôpitaux de Paris), Peter Petrow(Institut Curie), M. Beylot‐Barry(Centre Hospitalier Universitaire de Bordeaux), Nicole Basset‐Séguin(Assistance Publique – Hôpitaux de Paris), Lydia Deschamps(Assistance Publique – Hôpitaux de Paris), Jean‐Jacques Grob(Hôpital de la Timone), Brigitte Dréno(Centre Hospitalier Universitaire de Nantes), Isabelle Scheer-Senyarich(Assistance Publique – Hôpitaux de Paris), Coralie Bloch‐Queyrat(Assistance Publique – Hôpitaux de Paris), M.‐T. Leccia(Centre Hospitalier Universitaire de Grenoble), Andreea Stefan(Centre Hospitalier Universitaire de Caen Normandie), Philippe Saïag(Assistance Publique – Hôpitaux de Paris), Florent Grange(Centre Hospitalier Universitaire de Reims), Nicolás Meyer(Centre Hospitalier Universitaire de Toulouse), Julie De Quatrebarbes(Centre Hospitalier Annecy Genevois), Monica Dinulescu(Centre Eugène Marquis), Délphine Legoupil(Centre Hospitalier Régional Universitaire de Brest), L. Machet(Centre Hospitalier Universitaire de Tours), O. Dereure(Université de Montpellier), O. Zehou(Assistance Publique – Hôpitaux de Paris), Henri Montaudié(Centre Hospitalier Universitaire de Nice), E. Wierzbicka-Hainaut(Centre Hospitalier Universitaire de Poitiers), Yannick Le Corre(Centre Hospitalier Universitaire d'Angers), Sandrine Mansard(Centre Hospitalier Universitaire de Clermont-Ferrand), Sarah Guégan(Hôpital Cochin), Jean‐Philippe Arnault(Centre Hospitalier Universitaire Amiens-Picardie), S. Dalac(CHU Dijon Bourgogne), F. Aubin(Centre Hospitalier Universitaire de Besançon), Céline Alloux(Assistance Publique – Hôpitaux de Paris), Isabelle Lopez, Soufian Cherbal(Assistance Publique – Hôpitaux de Paris), Annick Tibi(Assistance Publique – Hôpitaux de Paris), Vincent Lévy(Université Sorbonne Paris Nord), on behalf of Groupe de Cancérologie Cutanée
Journal of Clinical Oncology
July 30, 2020
Cited by 173

Abstract

PURPOSE To evaluate first-line pembrolizumab monotherapy efficacy and safety in patients with unresectable cutaneous squamous cell carcinomas (CSCCs). PATIENTS AND METHODS Patients, predominantly men, with their CSSCs’ immunohistochemically determined programmed cell death-ligand 1 (PD-L1) status determined (tumor proportion score threshold, 1%), received pembrolizumab (200 mg every 3 weeks). The primary endpoint was the 39-patient primary cohort’s objective response rate at week 15 (ORR W15 ). Secondary objectives were best ORR, overall survival (OS), progression-free survival (PFS), duration of response (DOR), safety, ORR according to PD-L1 status and health-related quality of life using Functional Assessment of Cancer Therapy–General (FACT-G) score. An 18-patient expansion cohort, recruited to power the study to evaluate the ORR W15 difference between PD-L1+ and PD-L1– patients, was assessed for ORR, disease control rate, and safety, but not survival. RESULTS Median age of all patients was 79 years. The primary cohort’s ORR W15 was 41% (95% CI, 26% to 58%), including 13 partial and 3 complete responses. Best responses were 8 partial and 8 complete responses. At a median follow-up of 22.4 months, respective median PFS, DOR, and OS were 6.7 months, not reached, and 25.3 months, respectively. Pembrolizumab-related adverse events affected 71% of the patients, and 4 (7%) were grade ≥ 3. One death was related to rapid CSCC progression; another resulted from a fatal second aggressive head and neck squamous cell carcinoma diagnosed 15 weeks postinclusion. ORR W15 for the entire population was 42%; it was significantly higher for PD-L1+ patients (55%) versus PD-L1– patients (17%; P = .02). Responders’ W15 total FACT-G score had improved ( P = .025) compared with nonresponders. CONCLUSION First-line pembrolizumab monotherapy exhibited promising anti-CSCC activity, with durable responses and manageable safety. PD-L1 positivity appears to be predictive of pembrolizumab efficacy.


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