RECIST 1.1、mRECIST 和 Choi 标准,用于评估接受阿特珠单抗联合贝伐单抗治疗的肝细胞癌患者的治疗反应和生存结果。

IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
European Radiology Pub Date : 2025-02-01 Epub Date: 2024-07-30 DOI:10.1007/s00330-024-10986-z
Dong Hwan Kim, Eun Jeong Min, Bohyun Kim, Jong Young Choi, Jeong Won Jang, Pil Soo Sung, Ji Won Han, Hokun Kim, Joon-Il Choi
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引用次数: 0

摘要

研究目的我们旨在比较使用阿特珠单抗-贝伐单抗(atezo-bev)治疗的晚期HCC患者中,使用实体瘤反应评价标准(RECIST)1.1、改良RECIST(mRECIST)和Choi标准的早期反应者(定义为完全或部分反应者)率,并将其与无进展生存期(PFS)和总生存期(OS)相关联:这项回顾性研究纳入了接受atezo-bev治疗≥3个周期的晚期HCC患者。两名审查员在第一次随访成像时使用 RECIST 1.1、mRECIST 和 Choi 标准评估反应。卡普兰-梅耶曲线和对数秩检验评估并比较了PFS和OS。Cox 比例危险模型确定了生存结果预测因子。Kappa统计评估了读片者之间的一致性:我们评估了 77 名患者(65 名男性;平均年龄为 62.8 ± 12.3 岁)。崔氏标准显示的早期反应率最高(53.2%),超过了 mRECIST(32.5%-33.8%)和 RECIST 1.1(24.7%-26.0%),所有标准的一致性都非常好(κ,0.85-0.95)。在所有标准中,进展的患者人数一致(23-26 人),且与明显较差的 OS 相关(ps ≤ 0.049)。任何标准的应答者都显示较长的 PFS(ps ≤ 0.009)和 1 年 OS(ps ≤ 0.01)。Choi标准与明显更好的无地标OS相关(P = 0.003),应答者的1年OS率为76.9%,非应答者为38.1%。Cox分析发现,Choi标准的应答者是预测OS的重要指标:结论:与 RECIST 1.1 和 mRECIST 相比,Choi 标准能识别出更多的早期应答者,与改善的 OS 显著相关。结论:Choi标准比RECIST 1.1和mRECIST识别出更多的早期反应者,这与OS的改善有明显相关性。Choi标准可被视为新兴的阿特佐-贝夫系统治疗的正式反应评估标准:对于阿特佐-贝伐治疗晚期 HCC,更全面的反应标准(如 Choi 标准)可有效识别早期反应者,并与 RECIST 1.1 和 mRECIST 一起预测生存结果:要点:与mRECIST和RECIST1.1相比,Choi标准能在阿特佐-贝夫治疗后识别出更高比例的早期反应者。所有标准的应答者都有较长的 PFS 和 1 年 OS,只有 Choi 标准的应答者有较长的 OS,且没有地标时间。Choi标准以及RECIST1.1和mRECIST是阿特佐-贝夫治疗的有效反应评估工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

RECIST 1.1, mRECIST, and Choi criteria for evaluating treatment response and survival outcomes in hepatocellular carcinoma patients treated with atezolizumab plus bevacizumab.

RECIST 1.1, mRECIST, and Choi criteria for evaluating treatment response and survival outcomes in hepatocellular carcinoma patients treated with atezolizumab plus bevacizumab.

Objectives: We aimed to compare the early responder rates, defined as complete or partial responders, using response evaluation criteria in solid tumors (RECIST) 1.1, modified RECIST (mRECIST), and Choi criteria in advanced HCC patients treated with atezolizumab-bevacizumab (atezo-bev), and to correlate them with progression-free survival (PFS) and overall survival (OS).

Methods: This retrospective study included advanced HCC patients treated with ≥ 3 cycles of atezo-bev. Two reviewers assessed responses using RECIST 1.1, mRECIST, and Choi criteria at 1st follow-up imaging. Kaplan-Meier curves with log-rank tests evaluated and compared PFS and OS. Cox proportional hazard models identified survival outcome predictors. Kappa statistics assessed inter-reader agreement.

Results: We evaluated 77 patients (65 men; mean age, 62.8 ± 12.3 years). Choi's criteria revealed the highest early responders rate (53.2%), exceeding mRECIST (32.5-33.8%) and RECIST 1.1 (24.7-26.0%), with an excellent agreement in all criteria (κ, 0.85-0.95). Across criteria, a consistent number of patients progressed (23-26) and was associated with significantly poor OS (ps ≤ 0.049). Responders by any criteria showed longer PFS (ps ≤ 0.009), and 1-year OS (ps ≤ 0.01). Choi criteria linked to significantly better OS without landmark (p = 0.003), with 1-year OS rates at 76.9% for responders vs 38.1% for non-responders. Cox analysis identified responders by Choi criteria as a significant OS predictor.

Conclusion: Choi criteria identified more early responders than RECIST 1.1 and mRECIST, significantly correlating with improved OS. Choi criteria could be considered as a formal response assessment criterion for the emerging atezo-bev systemic treatment.

Clinical relevance statement: For atezo-bev treatment of advanced HCC, more comprehensive response criteria, such as Choi criteria, could be effective in identifying early responders and predicting survival outcomes along with RECIST 1.1 and mRECIST.

Key points: Choi criteria identified a higher rate of early responders compared to mRECIST and RECIST1.1 following atezo-bev treatment. Responders by all criteria had longer PFS and 1-year OS, and only those by Choi criteria experienced longer OS without landmark time. Choi criteria, with RECIST 1.1 and mRECIST, is an effective response assessment tool for atezo-bev treatment.

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来源期刊
European Radiology
European Radiology 医学-核医学
CiteScore
11.60
自引率
8.50%
发文量
874
审稿时长
2-4 weeks
期刊介绍: European Radiology (ER) continuously updates scientific knowledge in radiology by publication of strong original articles and state-of-the-art reviews written by leading radiologists. A well balanced combination of review articles, original papers, short communications from European radiological congresses and information on society matters makes ER an indispensable source for current information in this field. This is the Journal of the European Society of Radiology, and the official journal of a number of societies. From 2004-2008 supplements to European Radiology were published under its companion, European Radiology Supplements, ISSN 1613-3749.
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