Department of Thoracic-Head & Neck Med Onc, Division of Cancer Medicine, MD Anderson Cancer Center, Houston, TX, USA.
Radiation Oncology Department, Centre Leon Berard, Lyon, France.
Oncologist. 2022 Mar 4;27(2):e194-e198. doi: 10.1093/oncolo/oyab036.
In the randomized, phase 3 CheckMate 141 trial, nivolumab significantly improved overall survival (OS) versus investigator's choice (IC) of chemotherapy at primary analysis among 361 patients with recurrent or metastatic squamous cell carcinoma of the head and neck (R/M SCCHN) post-platinum therapy. Nivolumab versus IC as first-line treatment also improved OS among patients with R/M SCCHN who progressed on platinum therapy for locally advanced disease in the adjuvant or primary setting at 1-year follow-up. In the present long-term follow-up analysis of patients receiving first-line treatment, OS benefit with nivolumab (n = 50) versus IC (n = 26) was maintained (median: 7.7 months versus 3.3 months; hazard ratio: 0.56; 95% confidence interval, 0.34-0.94) at 2 years. No new safety signals were identified. In summary, this long-term 2-year analysis of CheckMate 141 supports the use of nivolumab as a first-line treatment for patients with platinum-refractory R/M SCCHN.
在随机、3 期 CheckMate 141 试验中,nivolumab 与研究者选择的化疗(IC)相比,在铂类治疗后复发或转移性头颈部鳞状细胞癌(R/M SCCHN)的 361 例患者中,在主要分析时显著改善了总生存期(OS)。在铂类治疗进展的局部晚期疾病辅助或新辅助治疗中,nivolumab 作为一线治疗也改善了 R/M SCCHN 患者的 OS,在 1 年随访时,OS 获益在 1 年随访时维持(中位:7.7 个月 vs. 3.3 个月;风险比:0.56;95%置信区间,0.34-0.94)。未发现新的安全性信号。总之,CheckMate 141 的这项 2 年长期随访分析支持 nivolumab 作为铂类难治性 R/M SCCHN 患者的一线治疗。