Department of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital & Institute, Beijing, China.
Department of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital & Institute, Beijing, China.
Int Immunopharmacol. 2024 Aug 20;137:112364. doi: 10.1016/j.intimp.2024.112364. Epub 2024 Jun 11.
Despite the widespread use of immune checkpoint inhibitors (ICIs) in cancer treatment, disease progression remains common in the majority of patients and subsequent therapeutic options for this population are limited. ICI rechallenge has been validated favorably in terms of efficacy and safety in many cancer types, while data in esophageal squamous cell carcinoma (ESCC) are still lacking.
Clinical and pathological characteristics of advanced ESCC patients who received ICI rechallenge were collected retrospectively. The primary outcomes of interest were the disease control rate (DCR) and progression-free survival (PFS). Treatment-related adverse events were also recorded. We categorized patients into primary resistance and secondary resistance based on a 6-month disease control duration following the initial immunotherapy and further conducted exploratory analyses.
A retrospective cohort study spanning January 2018 and October 2023, at Peking University Cancer Hospital, scrutinized 45 advanced ESCC patients undergoing two lines of ICI-based therapies (ICI-1 and ICI-2). The initial therapeutic approach involved combining ICIs with chemotherapy, and the ICI rechallenge primarily comprised ICIs and angiogenesis inhibitors. The median PFS for ICI-1 was 6.7 months with a disease control rate of 88.9 %. Following the ICI rechallenge, the median PFS and disease control rate remained at 3.2 months and 73.3 %, respectively. It is noteworthy that patients with secondary resistance to ICI-1 exhibited a higher 6-month PFS rate (29.6 % v.s. 11.1 %) in the ICI-2 stage. Any grade of treatment-related adverse events was observed in 29 (64.4 %) and 18 (40.0 %) patients at ICI-1 and ICI-2. The incidence of treatment-related adverse events in grades 3-4 was 9.1 % at ICI-1 and 9.1 % at ICI-2.
ICI rechallenge may offer a potential survival benefit and a favorable safety profile for patients with ESCC who have progressed after initial immunotherapy. Patients exhibiting acquired resistance during initial immunotherapy are more likely to achieve prolonged disease control after undergoing rechallenge therapy. Prospective studies are required to further explore the optimal combined therapy and select targeted population.
尽管免疫检查点抑制剂 (ICI) 在癌症治疗中广泛应用,但大多数患者仍会出现疾病进展,且该人群的后续治疗选择有限。ICI 重挑战在许多癌症类型中已被证明在疗效和安全性方面具有优势,而在食管鳞状细胞癌 (ESCC) 中的数据仍缺乏。
回顾性收集接受 ICI 重挑战的晚期 ESCC 患者的临床和病理特征。主要观察终点为疾病控制率 (DCR) 和无进展生存期 (PFS)。还记录了与治疗相关的不良事件。我们根据初始免疫治疗后 6 个月的疾病控制持续时间将患者分为原发性耐药和继发性耐药,并进一步进行了探索性分析。
本回顾性队列研究于 2018 年 1 月至 2023 年 10 月在北京大学肿瘤医院进行,纳入 45 例接受二线 ICI 为基础的治疗 (ICI-1 和 ICI-2) 的晚期 ESCC 患者。初始治疗方法为联合 ICI 与化疗,ICI 重挑战主要包括 ICI 和血管生成抑制剂。ICI-1 的中位 PFS 为 6.7 个月,疾病控制率为 88.9%。ICI-1 重挑战后,中位 PFS 和疾病控制率分别为 3.2 个月和 73.3%。值得注意的是,ICI-1 继发性耐药的患者在 ICI-2 阶段 6 个月的 PFS 率更高(29.6%比 11.1%)。ICI-1 和 ICI-2 时,分别有 29 例(64.4%)和 18 例(40.0%)患者发生任何级别治疗相关不良事件。ICI-1 时 3-4 级治疗相关不良事件的发生率为 9.1%,ICI-2 时为 9.1%。
ICI 重挑战可能为初始免疫治疗后进展的 ESCC 患者提供潜在的生存获益和良好的安全性。在初始免疫治疗期间出现获得性耐药的患者在接受重挑战治疗后更有可能获得长期疾病控制。需要前瞻性研究进一步探索最佳联合治疗方法和选择靶向人群。