San Diego Moores Cancer Center, University of California, San Diego, CA, USA.
Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada.
Lancet. 2019 Jan 12;393(10167):156-167. doi: 10.1016/S0140-6736(18)31999-8. Epub 2018 Nov 30.
BACKGROUND: There are few effective treatment options for patients with recurrent or metastatic head-and-neck squamous cell carcinoma. Pembrolizumab showed antitumour activity and manageable toxicity in early-phase trials. We aimed to compare the efficacy and safety of pembrolizumab versus standard-of-care therapy for the treatment of head-and-neck squamous cell carcinoma. METHODS: We did a randomised, open-label, phase 3 study at 97 medical centres in 20 countries. Patients with head-and-neck squamous cell carcinoma that progressed during or after platinum-containing treatment for recurrent or metastatic disease (or both), or whose disease recurred or progressed within 3-6 months of previous multimodal therapy containing platinum for locally advanced disease, were randomly assigned (1:1) in blocks of four per stratum with an interactive voice-response and integrated web-response system to receive pembrolizumab 200 mg every 3 weeks intravenously or investigator's choice of standard doses of methotrexate, docetaxel, or cetuximab intravenously (standard-of-care group). The primary endpoint was overall survival in the intention-to-treat population. Safety was analysed in the as-treated population. This trial is registered with ClinicalTrials.gov, number NCT02252042, and is no longer enrolling patients. FINDINGS: Between Dec 24, 2014, and May 13, 2016, 247 patients were randomly allocated to pembrolizumab and 248 were randomly allocated to standard of care. As of May 15, 2017, 181 (73%) of 247 patients in the pembrolizumab group and 207 (83%) of 248 patients in the standard-of-care group had died. Median overall survival in the intention-to-treat population was 8·4 months (95% CI 6·4-9·4) with pembrolizumab and 6·9 months (5·9-8·0) with standard of care (hazard ratio 0·80, 0·65-0·98; nominal p=0·0161). Fewer patients treated with pembrolizumab than with standard of care had grade 3 or worse treatment-related adverse events (33 [13%] of 246 vs 85 [36%] of 234). The most common treatment-related adverse event was hypothyroidism with pembrolizumab (in 33 [13%] patients) and fatigue with standard of care (in 43 [18%]). Treatment-related death occurred in four patients treated with pembrolizumab (unspecified cause, large intestine perforation, malignant neoplasm progression, and Stevens-Johnson syndrome) and two patients treated with standard of care (malignant neoplasm progression and pneumonia). INTERPRETATION: The clinically meaningful prolongation of overall survival and favourable safety profile of pembrolizumab in patients with recurrent or metastatic head and neck squamous cell carcinoma support the further evaluation of pembrolizumab as a monotherapy and as part of combination therapy in earlier stages of disease. FUNDING: Merck Sharp & Dohme, a subsidiary of Merck & Co.
背景:对于复发性或转移性头颈部鳞状细胞癌患者,目前有效的治疗选择有限。在早期试验中,派姆单抗显示出抗肿瘤活性和可管理的毒性。我们旨在比较派姆单抗与标准治疗对头颈部鳞状细胞癌的疗效和安全性。
方法:我们在 20 个国家的 97 个医学中心进行了一项随机、开放标签、3 期研究。患有复发性或转移性疾病(或两者兼有)期间或之后进展的头颈部鳞状细胞癌患者,或先前接受含铂的局部晚期疾病的多模式治疗后 3-6 个月内复发或进展的疾病患者,按每 4 个分层的块(1:1)随机分配,使用交互式语音应答和集成网络应答系统,每 3 周静脉注射 200 毫克派姆单抗或研究者选择的标准剂量甲氨蝶呤、多西他赛或西妥昔单抗静脉注射(标准治疗组)。主要终点是在意向治疗人群中的总生存期。安全性在治疗人群中进行分析。这项试验在 ClinicalTrials.gov 注册,编号为 NCT02252042,不再招募患者。
结果:2014 年 12 月 24 日至 2016 年 5 月 13 日,247 名患者被随机分配至派姆单抗组,248 名患者被随机分配至标准治疗组。截至 2017 年 5 月 15 日,派姆单抗组 247 名患者中有 181 名(73%)和标准治疗组 248 名患者中有 207 名(83%)死亡。意向治疗人群的中位总生存期为 8.4 个月(95%CI 6.4-9.4),派姆单抗组为 6.9 个月(5.9-8.0)(风险比 0.80,0.65-0.98;名义 p=0.0161)。接受派姆单抗治疗的患者中,3 级或更严重的治疗相关不良事件发生率低于接受标准治疗的患者(派姆单抗组 33 [13%],标准治疗组 85 [36%])。最常见的治疗相关不良事件是派姆单抗组的甲状腺功能减退症(33 例[13%])和标准治疗组的疲劳(43 例[18%])。派姆单抗治疗的 4 例患者(原因不明、大肠穿孔、恶性肿瘤进展和史蒂文斯-约翰逊综合征)和标准治疗的 2 例患者(恶性肿瘤进展和肺炎)发生了与治疗相关的死亡。
解释:派姆单抗在复发性或转移性头颈部鳞状细胞癌患者中的总生存期的显著延长和有利的安全性特征支持进一步评估派姆单抗作为单一疗法以及在疾病的早期阶段作为联合疗法的应用。
经费来源:默克公司的子公司默克 Sharp & Dohme。
J Cancer Res Clin Oncol. 2025-8-29
Curr Issues Mol Biol. 2025-8-1
MedComm (2020). 2025-8-10