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用于评估接受阿替利珠单抗联合贝伐单抗治疗的肝细胞癌患者治疗反应和生存结果的RECIST 1.1、mRECIST和Choi标准。

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

作者信息

Kim Dong Hwan, Min Eun Jeong, Kim Bohyun, Choi Jong Young, Jang Jeong Won, Sung Pil Soo, Han Ji Won, Kim Hokun, Choi Joon-Il

机构信息

Department of Radiology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.

Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.

出版信息

Eur Radiol. 2025 Feb;35(2):684-694. doi: 10.1007/s00330-024-10986-z. Epub 2024 Jul 30.

Abstract

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.

摘要

目的

我们旨在比较使用实体瘤疗效评价标准(RECIST)1.1、改良RECIST(mRECIST)和Choi标准评估的接受阿替利珠单抗-贝伐珠单抗(阿替利珠单抗-贝伐单抗)治疗的晚期肝癌患者的早期缓解率(定义为完全或部分缓解者),并将其与无进展生存期(PFS)和总生存期(OS)相关联。

方法

这项回顾性研究纳入了接受≥3个周期阿替利珠单抗-贝伐单抗治疗的晚期肝癌患者。两名评估者在首次随访影像检查时使用RECIST 1.1、mRECIST和Choi标准评估疗效。采用对数秩检验的Kaplan-Meier曲线评估和比较PFS和OS。Cox比例风险模型确定生存结果预测因素。Kappa统计量评估评估者间的一致性。

结果

我们评估了77例患者(65例男性;平均年龄62.8±12.3岁)。Choi标准显示出最高的早期缓解率(53.2%),超过mRECIST(32.5%-33.8%)和RECIST 1.1(24.7%-26.0%),所有标准的一致性都很好(κ,0.85-0.95)。在所有标准中,进展的患者数量一致(23-26例),且与显著较差的OS相关(P≤0.049)。任何标准下的缓解者均显示出更长的PFS(P≤0.009)和1年OS(P≤0.01)。Choi标准与无时间节点的显著更好的OS相关(P=0.003),缓解者的1年OS率为76.9%,未缓解者为38.1%。Cox分析确定Choi标准下的缓解者是OS的显著预测因素。

结论

与RECIST 1.1和mRECIST相比,Choi标准识别出更多的早期缓解者,与改善的OS显著相关。Choi标准可被视为新兴的阿替利珠单抗-贝伐单抗全身治疗的正式疗效评估标准。

临床相关性声明

对于阿替利珠单抗-贝伐单抗治疗晚期肝癌,更全面的疗效标准,如Choi标准,与RECIST 1.1和mRECIST一样,在识别早期缓解者和预测生存结果方面可能是有效的。

关键点

与阿替利珠单抗-贝伐单抗治疗后的mRECIST和RECIST1.1相比,Choi标准识别出更高比例的早期缓解者。所有标准下的缓解者均有更长的PFS和1年OS,只有Choi标准下的缓解者在无时间节点时经历了更长的OS。Choi标准与RECIST 1.1和mRECIST一样,是阿替利珠单抗-贝伐单抗治疗的有效疗效评估工具。

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