Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.
Department of Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Esophagus. 2022 Jan;19(1):137-145. doi: 10.1007/s10388-021-00877-3. Epub 2021 Sep 30.
Safe and effective treatments for advanced esophageal cancer are an unmet need in Japan. We report results of a subgroup analysis of Japanese patients enrolled in KEYNOTE-181, a randomized, open-label, phase 3 study of pembrolizumab versus chemotherapy as second-line therapy for patients with advanced or metastatic esophageal cancer whose disease progressed after standard first-line therapy.
Patients were randomly assigned 1:1 to receive pembrolizumab 200 mg every 3 weeks or investigator's choice of paclitaxel, docetaxel, or irinotecan. Efficacy was evaluated in all Japanese patients and in those with programmed death ligand 1 combined positive score ≥ 10.
Of the 152 Japanese patients enrolled (pembrolizumab, n = 77; chemotherapy, n = 75), 150 (98.7%) had squamous cell carcinoma and 79 (52.0%) had combined positive score ≥ 10. At the final analysis, median overall survival was improved among all patients (12.4 vs 8.2 months with pembrolizumab and chemotherapy, respectively; hazard ratio, 0.68; 95% CI 0.48-0.97) and patients with combined positive score ≥ 10 (12.6 vs 8.4 months; hazard ratio, 0.68; 95% CI 0.42-1.10). Fewer patients had any-grade (74.0% vs 95.9%) or grade 3-5 (16.9 vs 50.0%) treatment-related adverse events with pembrolizumab than with chemotherapy.
Consistent with the global trial results, second-line pembrolizumab therapy showed a survival benefit and a favorable safety profile compared with chemotherapy in Japanese patients with advanced esophageal cancer.
安全有效的治疗方法是晚期食管癌患者的未满足需求。我们报告了 KEYNOTE-181 研究中日本患者亚组分析的结果,该研究是一项随机、开放标签、三期研究,评估了帕博利珠单抗与化疗二线治疗局部晚期或转移性食管癌患者的疗效,这些患者在标准一线治疗后疾病进展。
患者以 1:1 的比例随机分配接受帕博利珠单抗 200mg 每 3 周一次或研究者选择紫杉醇、多西他赛或伊立替康。在所有日本患者和程序性死亡配体 1 联合阳性评分≥10 的患者中评估了疗效。
152 名日本患者入组(帕博利珠单抗组 n=77;化疗组 n=75),150 名(98.7%)患者为鳞状细胞癌,79 名(52.0%)患者为联合阳性评分≥10。最终分析时,所有患者的中位总生存期均得到改善(帕博利珠单抗组和化疗组分别为 12.4 个月和 8.2 个月;风险比,0.68;95%置信区间,0.48-0.97),联合阳性评分≥10 的患者也得到改善(12.6 个月和 8.4 个月;风险比,0.68;95%置信区间,0.42-1.10)。帕博利珠单抗治疗组患者发生任何等级(74.0% vs 95.9%)或 3-5 级(16.9% vs 50.0%)治疗相关不良事件的人数少于化疗组。
与全球试验结果一致,二线帕博利珠单抗治疗与化疗相比,为日本晚期食管癌患者带来了生存获益和良好的安全性。