Outcomes of post-immunotherapy durable responders of advanced hepatocellular carcinoma - with emphasis on locoregional therapy for oligoprogression

Liver Cancer Pub Date : 2024-02-01 DOI:10.1159/000536549
Tsung-Hao Liu, San-Chi Chen, Kun-Ming Rau, Li‐Chun Lu, Po-Ting Lin, Yung-Yeh Su, Wei Teng, Shiue-Wei Lai, Ren-Hua Yeh, T. Kao, Pei‐Chang Lee, Chi-Jung Wu, Chien-Hung Chen, Chih-Hung Hsu, Shi-Ming Lin, Yi-Hsiang Huang, Li-Tzong Chen, Ann-Lii Cheng, Ying-Chun Shen
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Abstract

Introduction The progression patterns, dispositions, and outcomes of patients with advanced hepatocellular carcinoma (HCC) who achieved durable responses with immunotherapy remain poorly characterized. Methods Patients with advanced HCC who received immune checkpoint inhibitor (ICI)-based immunotherapy and achieved durable responses were retrospectively included. A durable response was defined as partial response (PR) or stable disease (SD) per RECIST 1.1 for more than 8 months after initiation of immunotherapy. Oligoprogression and polyprogression were defined as progression at ≤ 3 and > 3 lesions, respectively. Results A total of 91 durable responders (63 PR and 28 SD) were identified. The majority had chronic viral hepatitis (n=69, 75.8%). Forty-seven (51.6%) and 44 (48.4%) patients received the index immunotherapy as first-line and second or beyond-line therapy, respectively. Fifty-four (59.3%) patients subsequently developed progression, with a predominant pattern of oligoprogression (66.7%). The median overall survival (OS) was 46.2 months (95% CI: 34.1–58.3). For patients with subsequent progression, employment of locoregional therapy (LRT) for progression was associated with prolonged OS (univariate analysis: hazard ratio [HR] 0.397, p=0.009; multivariate analysis: HR 0.363, p=0.050). Patients with oligoprogression who received LRT showed longer median OS than those who did not (48.4 vs. 20.5 months, p<0.001). In contrast, the median OS of patients with polyprogression who received LRT was not different from those without LRT (27.7 vs. 25.5 months, p=0.794). Conclusion Approximately 60% of the post-immunotherapy durable responders of HCC subsequently develop progression. Proactive LRT may further rescue patients who develop subsequent oligoprogression. Prospective studies are mandatory to clarify the proper management of durable responders with subsequent progression.
晚期肝细胞癌免疫治疗后持久应答者的疗效--重点是寡进展的局部治疗
简介:接受免疫疗法并获得持久应答的晚期肝细胞癌(HCC)患者的进展模式、处置和预后特征仍然不甚明了。方法回顾性纳入接受基于免疫检查点抑制剂(ICI)的免疫疗法并获得持久应答的晚期HCC患者。根据RECIST 1.1标准,持久应答的定义为免疫治疗开始后8个月以上的部分应答(PR)或疾病稳定(SD)。寡病变进展和多病变进展的定义分别为≤3个和>3个病变的进展。结果 共发现 91 例持久应答者(63 例 PR 和 28 例 SD)。大多数患者患有慢性病毒性肝炎(69 人,75.8%)。47例(51.6%)和44例(48.4%)患者分别将指标免疫疗法作为一线疗法和二线或二线以上疗法。54例(59.3%)患者随后出现了病情进展,其中以少进展为主(66.7%)。中位总生存期(OS)为 46.2 个月(95% CI:34.1-58.3)。对于随后出现进展的患者,采用局部区域疗法(LRT)治疗进展与OS延长相关(单变量分析:危险比[HR] 0.397,P=0.009;多变量分析:HR 0.363,P=0.050)。与未接受 LRT 治疗的患者相比,接受 LRT 治疗的寡进展患者的中位生存期更长(48.4 个月对 20.5 个月,P<0.001)。相比之下,接受LRT治疗的多发性进展患者的中位OS与未接受LRT治疗的患者没有差异(27.7个月 vs. 25.5个月,p=0.794)。积极的 LRT 可进一步挽救随后出现寡进展的患者。必须开展前瞻性研究,以明确如何妥善处理后续进展的持久应答者。
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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