Durvalumab with or without tremelimumab versus the EXTREME regimen as first-line treatment for recurrent or metastatic squamous cell carcinoma of the head and neck: KESTREL, a randomized, open-label, phase III study

银耳霉素 杜瓦卢马布 医学 养生 头颈部鳞状细胞癌 内科学 危险系数 肿瘤科 西妥昔单抗 置信区间 头颈部癌 癌症 免疫疗法 易普利姆玛 无容量 结直肠癌
作者
Amanda Psyrri,Jérôme Fayette,Kevin J. Harrington,Maura L. Gillison,M-J. Ahn,Shunji Takahashi,Jared Weiss,J-P Machiels,Shrujal S. Baxi,Alexander Vasilyev,Andrey Karpenko,Mikhail Dvorkin,Ching-Yun Hsieh,Satheesh Chiradoni Thungappa,Pedro Pérez Segura,Ihor Vynnychenko,Robert I. Haddad,Stefan Kasper,Paul-Stefan Mauz,V Baker,Philip He,Brent Evans,Sophie Wildsmith,Rolf Olsson,Alejandro Yovine,John F. Kurland,Nassim Morsli,Tanguy Y. Seiwert
出处
期刊:Annals of Oncology [Elsevier]
卷期号:34 (3): 262-274 被引量:39
标识
DOI:10.1016/j.annonc.2022.12.008
摘要

Patients with recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC) have a poor prognosis. The phase III KESTREL study evaluated the efficacy of durvalumab [programmed death-ligand 1 (PD-L1) antibody] with or without tremelimumab [cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) antibody], versus the EXTREME regimen in patients with R/M HNSCC.Patients with HNSCC who had not received prior systemic treatment for R/M disease were randomized (2 : 1 : 1) to receive durvalumab 1500 mg every 4 weeks (Q4W) plus tremelimumab 75 mg Q4W (up to four doses), durvalumab monotherapy 1500 mg Q4W, or the EXTREME regimen (platinum, 5-fluorouracil, and cetuximab) until disease progression. Durvalumab efficacy, with or without tremelimumab, versus the EXTREME regimen in patients with PD-L1-high tumors and in all randomized patients was assessed. Safety was also assessed.Durvalumab and durvalumab plus tremelimumab were not superior to EXTREME for overall survival (OS) in patients with PD-L1-high expression [median, 10.9 and 11.2 versus 10.9 months, respectively; hazard ratio (HR) = 0.96; 95% confidence interval (CI) 0.69-1.32; P = 0.787 and HR = 1.05; 95% CI 0.80-1.39, respectively]. Durvalumab and durvalumab plus tremelimumab prolonged duration of response versus EXTREME (49.3% and 48.1% versus 9.8% of patients remaining in response at 12 months), correlating with long-term OS for responding patients; however, median progression-free survival was longer with EXTREME (2.8 and 2.8 versus 5.4 months). Exploratory analyses suggested that subsequent immunotherapy use by 24.3% of patients in the EXTREME regimen arm contributed to the similar OS outcomes between arms. Grade 3/4 treatment-related adverse events (TRAEs) for durvalumab, durvalumab plus tremelimumab, and EXTREME were 8.9%, 19.1%, and 53.1%, respectively.In patients with PD-L1-high expression, OS was comparable between durvalumab and the EXTREME regimen. Durvalumab alone, and with tremelimumab, demonstrated durable responses and reduced TRAEs versus the EXTREME regimen in R/M HNSCC.
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