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Radiologic Response Assessment With RECIST 1.1 and mRECIST in Patients With Hepatocellular Carcinoma Treated With Atezolizumab Plus Bevacizumab

Authors
 Jeong, Boryeong  ;  Park, Hyo Jung  ;  Choi, Won-Mook  ;  Choi, Sang Hyun  ;  Kim, Kyung Won  ;  Kim, So Yeon  ;  Lee, Seung Soo 
Citation
 KOREAN JOURNAL OF RADIOLOGY, Vol.27(5) : 428-439, 2026-05 
Journal Title
KOREAN JOURNAL OF RADIOLOGY
ISSN
 1229-6929 
Issue Date
2026-05
MeSH
Antibodies, Monoclonal, Humanized ; Antineoplastic Combined Chemotherapy Protocols* / therapeutic use ; Bevacizumab* / administration & dosage ; Bevacizumab* / therapeutic use ; Carcinoma, Hepatocellular* / diagnostic imaging ; Carcinoma, Hepatocellular* / drug therapy ; Carcinoma, Hepatocellular* / mortality ; Female ; Humans ; Liver Neoplasms / diagnostic imaging ; Liver Neoplasms / drug therapy ; Male ; Response Evaluation Criteria in Solid Tumors ; Retrospective Studies ; Treatment Outcome
Keywords
Response evaluation criteria in solid tumors ; Carcinoma ; Hepatocellular ; Atezolizumab ; Bevacizumab ; Survival
Abstract
Objective: Evidence remains limited regarding whether Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) or modified RECIST (mRECIST) more reliably assesses treatment response in patients with hepatocellular carcinoma (HCC) receiving atezolizumab plus bevacizumab (Atezo/Bev). This study aimed to evaluate response patterns based on RECIST 1.1 and mRECIST, analyze inter-reader agreement, and assess their prognostic value for overall survival (OS) in patients with HCC receiving first-line Atezo/Bev. Materials and Methods: This retrospective study included patients with HCC treated with first-line Atezo/Bev between June 2020 and December 2022 at a tertiary center. Patients with at least one hypervascular hepatic target lesion were eligible. Two radiologists independently assessed treatment responses using RECIST 1.1 and mRECIST. Inter-reader agreement was evaluated using Cohen's kappa coefficient. Time-dependent Cox regression analysis was performed, with radiologic response and progression treated as time-varying covariates. Prognostic discrimination was evaluated using Harrell's concordance index (C-index). Results: A total of 207 patients were included (171 men; median age, 63 years; median follow-up, 10.7 months [range, 0.8- 46.4 months]; median OS, 10.7 months [95% confidence interval, 9.2-12.8 months]). mRECIST identified more responders than RECIST 1.1 (54.6% vs. 16.9%). RECIST 1.1 demonstrated excellent inter-reader agreement, whereas mRECIST showed substantial agreement (weighted kappa, 0.89 vs. 0.79). A significantly higher rate of dissociated responses was observed with mRECIST than with RECIST 1.1 (14.0% vs. 4.3%, P < 0.001). Both RECIST 1.1- and mRECIST-based responses and progression were independently associated with OS. Models incorporating RECIST 1.1 demonstrated slightly higher C-index values than those incorporating mRECIST (RECIST 1.1: 0.68 for response and 0.75 for progression; mRECIST: 0.65 and 0.70, respectively). Conclusion: RECIST 1.1 is more reproducible and prognostically valuable for guiding treatment decisions in patients with HCC receiving first-line Atezo/Bev. However, this does not invalidate the use of mRECIST as a biological tumor response marker.
Files in This Item:
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DOI
10.3348/kjr.2025.1849
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers
Yonsei Authors
Jeong, Boryeong(정보령)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/212487
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