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

Authors :
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
Tsui-Mai 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
Source :
Liver Cancer (2024)
Publication Year :
2024
Publisher :
Karger Publishers, 2024.

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

Details

Language :
English
ISSN :
16645553
Database :
Directory of Open Access Journals
Journal :
Liver Cancer
Publication Type :
Academic Journal
Accession number :
edsdoj.982567d91e37462383001cc9dc3d4719
Document Type :
article
Full Text :
https://doi.org/10.1159/000536549