Pembrolizumab With or Without Chemotherapy in Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma: Updated Results of the Phase III KEYNOTE-048 Study

Kevin J. Harrington(Royal Marsden NHS Foundation Trust), Barbara Burtness(Yale Cancer Center), Richard Greil(Paracelsus Medical University), Denis Soulières(Centre Hospitalier de l’Université de Montréal), Makoto Tahara(National Cancer Center Hospital East), Gilberto de Castro(Instituto do Câncer do Estado de São Paulo), Amanda Psyrri(National and Kapodistrian University of Athens), Irene Braña(Vall d'Hebron Hospital Universitari), Neus Basté(Vall d'Hebron Hospital Universitari), Prakash Neupane(University of Kansas Medical Center), Åse Bratland(Oslo University Hospital), Thorsten Fuereder(Medical University of Vienna), Brett Hughes(The University of Queensland), Ricard Mesı́a, Nuttapong Ngamphaiboon(Mahidol University), Tamara Rordorf(University Hospital of Zurich), Wan Zamaniah Wan Ishak(University of Malaya), Jianxin Lin(Merck & Co., Inc., Rahway, NJ, USA (United States)), Burak Gümüşçü(Merck & Co., Inc., Rahway, NJ, USA (United States)), Ramona F. Swaby(Merck & Co., Inc., Rahway, NJ, USA (United States)), Danny Rischin(The University of Melbourne)
Journal of Clinical Oncology
October 11, 2022
Cited by 480Open Access
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Abstract

PURPOSE: Pembrolizumab and pembrolizumab-chemotherapy demonstrated efficacy in recurrent/metastatic head and neck squamous cell carcinoma in KEYNOTE-048. Post hoc analysis of long-term efficacy and progression-free survival on next-line therapy (PFS2) is presented. METHODS: Patients were randomly assigned (1:1:1) to pembrolizumab, pembrolizumab-chemotherapy, or cetuximab-chemotherapy. Efficacy was evaluated in programmed death ligand 1 (PD-L1) combined positive score (CPS) ≥ 20, CPS ≥ 1, and total populations, with no multiplicity or alpha adjustment. RESULTS: The median study follow-up was 45.0 months (interquartile range, 41.0-49.2; n = 882). At data cutoff (February 18, 2020), overall survival improved with pembrolizumab in the PD-L1 CPS ≥ 20 (hazard ratio [HR], 0.61; 95% CI, 0.46 to 0.81) and CPS ≥ 1 populations (HR, 0.74; 95% CI, 0.61 to 0.89) and was noninferior in the total population (HR, 0.81; 95% CI, 0.68 to 0.97). Overall survival improved with pembrolizumab-chemotherapy in the PD-L1 CPS ≥ 20 (HR, 0.62; 95% CI, 0.46 to 0.84), CPS ≥ 1 (HR, 0.64; 95% CI, 0.53 to 0.78), and total (HR, 0.71; 95% CI, 0.59 to 0.85) populations. The objective response rate on second-course pembrolizumab was 27.3% (3 of 11). PFS2 improved with pembrolizumab in the PD-L1 CPS ≥ 20 (HR, 0.64; 95% CI, 0.48 to 0.84) and CPS ≥ 1 (HR, 0.79; 95% CI, 0.66 to 0.95) populations and with pembrolizumab-chemotherapy in the PD-L1 CPS ≥ 20 (HR, 0.64; 95% CI, 0.48 to 0.86), CPS ≥ 1 (HR, 0.66; 95% CI, 0.55 to 0.81), and total (HR, 0.73; 95% CI, 0.61 to 0.88) populations. PFS2 was similar after pembrolizumab and longer after pembrolizumab-chemotherapy on next-line taxanes and shorter after pembrolizumab and similar after pembrolizumab-chemotherapy on next-line nontaxanes. CONCLUSION: With a 4-year follow-up, first-line pembrolizumab and pembrolizumab-chemotherapy continued to demonstrate survival benefit versus cetuximab-chemotherapy in recurrent/metastatic head and neck squamous cell carcinoma. Patients responded well to subsequent treatment after pembrolizumab-based therapy.


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