Morita Ryuichi, Ishikawa Takeshi, Doi Toshifumi, Itani Junichiro, Sone Daiki, Iwai Naoto, Inoue Ken, Konishi Hirotaka, Dohi Osamu, Yoshida Naohisa, Shiozaki Atsushi, Uchiyama Kazuhiko, Takagi Tomohisa, Fujiwara Hitoshi, Konishi Hideyuki, Itoh Yoshito
Department of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto, Kyoto 602-8566, Japan.
Oncology Unit, University Hospital of Kyoto Prefectural University of Medicine, Kyoto, Kyoto 602-8566, Japan.
Oncol Lett. 2025 Jan 17;29(3):145. doi: 10.3892/ol.2025.14891. eCollection 2025 Mar.
Nivolumab has been approved for unresectable recurrent advanced esophageal cancer. The present study aimed to provide real-world data on diverse patient profiles, including the elderly and those with poor performance status, while exploring therapeutic efficacy biomarkers. This retrospective study included 42 patients with esophageal cancer who received nivolumab after second- or later-line treatment at Kyoto Prefectural University of Medicine (Kyoto, Japan) from February 2020 to December 2021. The study evaluated real-world patient data for the outcomes, safety and clinical characteristics impacting efficacy. The median patient age was 70 years (range, 52-80), and 36 patients (85%) were male. A total of 22 patients (52%) were ≥70 years of age, and three (7%) had an Eastern Clinical Oncology Group Performance Status of 2, which was not included in the clinical trial. The response and disease control rates were 26 and 78%, respectively. With a median follow-up period of 7.9 months, the median progression-free survival and overall survival were 3.5 (95% CI, 2.0-6.0) and 19 (95% CI, 6.4-not reached) months, respectively. Patients with liver metastases had significantly worse progression-free survival and overall survival, while lung and lymph node metastases did not clearly impact nivolumab efficacy. Multivariate analysis revealed that liver metastases may predict both worse progression-free survival [hazard ratio (HR) 2.37; 95% CI, 1.07-5.24; P=0.03) and overall survival (HR, 2.75; 95% CI, 1.00-7.53; P=0.04). This study provided real-world evidence of nivolumab's favorable efficacy across diverse profiles, including the elderly and those with impaired performance status. No serious immune-related adverse events occurred and liver metastasis emerged as a predictive biomarker for nivolumab efficacy in esophageal squamous cell cancer.
纳武利尤单抗已被批准用于不可切除的复发性晚期食管癌。本研究旨在提供关于不同患者特征(包括老年人和身体状况较差者)的真实世界数据,同时探索治疗疗效生物标志物。这项回顾性研究纳入了42例食管癌患者,这些患者于2020年2月至2021年12月在日本京都府立医科大学接受二线或后续治疗后使用了纳武利尤单抗。该研究评估了影响疗效的真实世界患者数据,包括结局、安全性和临床特征。患者的中位年龄为70岁(范围52 - 80岁),36例(85%)为男性。共有22例(52%)患者年龄≥70岁,3例(7%)东部肿瘤协作组体能状态为2,这在临床试验中未纳入。缓解率和疾病控制率分别为26%和78%。中位随访期为7.9个月,中位无进展生存期和总生存期分别为3.5(95%CI,2.0 - 6.0)个月和19(95%CI,6.4 - 未达到)个月。肝转移患者的无进展生存期和总生存期显著更差,而肺和淋巴结转移对纳武利尤单抗疗效无明显影响。多因素分析显示,肝转移可能预示无进展生存期更差[风险比(HR)2.37;95%CI,1.07 - 5.24;P = 0.03]和总生存期更差(HR,2.75;95%CI,1.00 - 7.53;P = 0.04)。本研究提供了纳武利尤单抗在包括老年人和身体状况受损者在内的不同患者特征中疗效良好的真实世界证据。未发生严重的免疫相关不良事件,肝转移成为食管鳞状细胞癌中纳武利尤单抗疗效的预测生物标志物。