Real-world clinical impact of first-line immune checkpoint inhibitor-based therapy in advanced esophageal squamous cell carcinoma

M. Tamba , K. Chin , H. Osumi , M. Ogura , S. Fukuoka , S. Udagawa , K. Shimozaki , K. Yoshino , T. Wakatsuki , E. Shinozaki , K. Yamaguchi , A. Ooki
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Abstract

Background

Chemotherapy (chemo) combined with an immune checkpoint inhibitor (ICI) or dual ICI therapy with nivolumab and ipilimumab (nivo + ipi) is the standard first-line treatment for patients with advanced esophageal squamous cell carcinoma (ESCC). In this study, we evaluated real-world clinical outcomes for first-line ICI-based therapy and explored its prognostic factors.

Patients and methods

This single-center retrospective study included patients with ESCC who received ICI-based therapy between January 2021 and July 2024.

Results

In total, 92 patients received either ICI + chemo (n = 60) or nivo + ipi (n = 32). The median progression-free survival and overall survival (OS) were 5.0 and 16.0 months for ICI + chemo and 3.5 and 16.9 months for nivo + ipi, respectively. Of the 70 patients with measurable lesions, early tumor shrinkage (ETS) was achieved in 37% for ICI + chemo and 33% for nivo + ipi. ETS was significantly associated with a lower performance status and neutrophil-to-lymphocyte ratios, but not with the treatment regimen or programmed death-ligand 1 (PD-L1) status. Patients who achieved ETS showed significant tumor reduction and a durable response. ETS was an independent predictor of favorable OS (hazard ratio 0.34, 95% confidence interval 0.11-0.88, P = 0.04), whereas neither the treatment regimen nor the PD-L1 status influenced OS. Immune-related adverse events of grade ≥3 occurred in 12% of patients.

Conclusions

First-line immunotherapy is effective and safe for the treatment of patients with ESCC. Rapid and deep tumor shrinkage may serve as an early predictive biomarker for longer survival.
一线免疫检查点抑制剂治疗晚期食管鳞状细胞癌的实际临床影响
化疗(chemo)联合免疫检查点抑制剂(ICI)或nivolumab和ipilimumab (nivo + ipi)的双重ICI治疗是晚期食管鳞状细胞癌(ESCC)患者的标准一线治疗。在这项研究中,我们评估了一线ci治疗的真实临床结果,并探讨了其预后因素。患者和方法本单中心回顾性研究纳入了2021年1月至2024年7月期间接受基于ici治疗的ESCC患者。结果共92例患者接受了ICI +化疗(60例)或nivo + ipi化疗(32例)。ICI +化疗的中位无进展生存期和总生存期(OS)分别为5.0和16.0个月,nivo + ipi化疗的中位无进展生存期和总生存期分别为3.5和16.9个月。在70例可测量病变的患者中,37%的ICI +化疗患者和33%的nivo + ipi患者实现了早期肿瘤缩小(ETS)。ETS与较低的表现状态和中性粒细胞与淋巴细胞比率显著相关,但与治疗方案或程序性死亡配体1 (PD-L1)状态无关。达到ETS的患者表现出显著的肿瘤缩小和持久的反应。ETS是有利OS的独立预测因子(风险比0.34,95%可信区间0.11-0.88,P = 0.04),而治疗方案和PD-L1状态均不影响OS。12%的患者发生≥3级免疫相关不良事件。结论一线免疫疗法治疗ESCC是安全有效的。快速和深度的肿瘤缩小可以作为延长生存期的早期预测性生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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