Ronot Maxime, Bouattour Mohamed, Wassermann Johanna, Bruno Onorina, Dreyer Chantal, Larroque Béatrice, Castera Laurent, Vilgrain Valérie, Belghiti Jacques, Raymond Eric, Faivre Sandrine
Departments of Radiology, Hepatology, Medical Oncology, Biostatistics, and Hepatobiliary and Pancreatic Surgery, Beaujon University Hospital, Assistance Publique Hopitaux de Paris, Clichy, France.
Oncologist. 2014 Apr;19(4):394-402. doi: 10.1634/theoncologist.2013-0114. Epub 2014 Mar 20.
Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1), may underestimate activity and does not predict survival in patients with hepatocellular carcinoma (HCC) treated with sorafenib. This study assessed the value of alternative radiological criteria to evaluate response in HCC patients treated with sorafenib.
A retrospective blinded central analysis was performed of computed tomography (CT) scans from baseline and the first tumor evaluation in consecutive patients treated with sorafenib over a 2-year period in a single institution. Four different evaluation criteria were used: Choi, European Association for the Study of the Liver (EASL), modified RECIST (mRECIST), and RECIST 1.1.
Among 82 HCC patients, 64 with Barcelona Clinic Liver Cancer stage B-C were evaluable with a median follow-up of 22 months. Median duration of sorafenib treatment was 5.7 months, and median overall survival was 12.8 months. At the time of the first CT scan, performed after a median of 2.1 months, Choi, EASL, mRECIST, and RECIST 1.1 identified 51%, 28%, 28%, and 3% objective responses, respectively. Responders by all criteria showed consistent overall survival >20 months. Among patients with stable disease according to RECIST 1.1, those identified as responders by Choi had significantly better overall survival than Choi nonresponders (22.4 vs. 10.6 months; hazard ratio: 0.43, 95% confidence interval: 0.15-0.86, p = .0097).
Choi, EASL, and mRECIST criteria appear more appropriate than RECIST 1.1 to identify responders with long survival among advanced HCC patients benefiting from sorafenib.
实体瘤疗效评价标准1.1版(RECIST 1.1)可能会低估索拉非尼治疗的肝细胞癌(HCC)患者的活性,且无法预测其生存情况。本研究评估了其他影像学标准在评价索拉非尼治疗的HCC患者疗效方面的价值。
对某单一机构在2年期间连续接受索拉非尼治疗患者的基线及首次肿瘤评估时的计算机断层扫描(CT)进行回顾性盲法中心分析。使用了四种不同的评估标准:Choi标准、欧洲肝脏研究协会(EASL)标准、改良RECIST(mRECIST)标准和RECIST 1.1标准。
在82例HCC患者中,64例巴塞罗那临床肝癌分期为B - C期的患者可进行评估,中位随访时间为22个月。索拉非尼治疗的中位持续时间为5.7个月,中位总生存期为12.8个月。在中位2.1个月后进行的首次CT扫描时,Choi标准、EASL标准、mRECIST标准和RECIST 1.1标准分别识别出51%、28%、28%和3%的客观缓解。所有标准的缓解者总生存期均一致>20个月。在根据RECIST 1.1标准判定为疾病稳定的患者中,被Choi标准判定为缓解者的总生存期显著优于Choi标准判定为未缓解者(22.4 vs. 10.6个月;风险比:0.43,95%置信区间:0.15 - 0.86,p = .0097)。
Choi标准、EASL标准和mRECIST标准在识别从索拉非尼治疗中获益的晚期HCC患者中长生存期缓解者方面似乎比RECIST 1.1标准更合适。