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CRAFITY评分与甲胎蛋白反应相结合可预测阿替利珠单抗联合贝伐单抗治疗不可切除肝细胞癌的良好预后。

Combination of CRAFITY score with Alpha-fetoprotein response predicts a favorable outcome of atezolizumab plus bevacizumab for unresectable hepatocellular carcinoma.

作者信息

Teng Wei, Lin Chen-Chun, Su Chung-Wei, Lin Po-Ting, Hsieh Yi-Chung, Chen Wei-Ting, Ho Ming-Mo, Wang Ching-Ting, Chai Pei-Mei, Hsieh Jason Chia-Hsun, Lin Chun-Yen, Lin Shi-Ming

机构信息

Department of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Linkou Medical Center Taiwan.

College of Medicine, Chang Gung University Taiwan.

出版信息

Am J Cancer Res. 2022 Apr 15;12(4):1899-1911. eCollection 2022.

Abstract

Immune checkpoint inhibitors (ICIs) with atezolizumab plus bevacizumab are promising agents for unresectable hepatocellular carcinoma (HCC). We tried to guide the treatment based on recent developed CRAFITY score combining with on-treatment AFP response. Eighty-nine patients who received atezolizumab plus bevacizumab regardless of as a first-line therapy or not for unresectable HCC were enrolled for analyses. Radiologic evaluation was based on modified Response Evaluation Criteria in Solid Tumors (mRECIST). The objective response rate (ORR) and disease control rate (DCR) were 25.0% and 65.5%, respectively. Multivariate analysis showed that low CRAFITY score (AFP<100 ng/ml or CRP<10 mg/l) and satisfactory AFP response at 6 weeks (≥75% decrease or ≤10% increase from baseline) were independent factors determining good overall survival (OS) (hazard ratio [HR]=0.143, P=0.002 & HR=0.337, P=0.031), progression-free survival (PFS) (HR=0.419, P=0.022 & HR=0.429, P=0.025) and good responder (odds ratio [OR]=1.763, P=0.044 & OR=3.881, P=0.011). Patients were further divided into three classes by combination of CRAFITY score and AFP response at 6 weeks [The CAR (CRAFITY score and AFP-Response) classification)]: low CRAFITY score with satisfactory AFP response at 6 weeks (class I), either high CRAFITY score or unsatisfactory AFP response at 6 weeks (class II) and high CRAFITY score together with unsatisfactory AFP response at 6 weeks (class III). ORR was 35.0%, 18.2%, and 0% in class I, II and III patients, respectively (overall P=0.034). Patients in the class I had the best OS and PFS, followed by class II and class III (median OS: not reached vs. 11.1 vs. 4.3 months, log-rank P<0.001; median PFS: 7.9 vs. 6.6 vs. 2.6 months, log-rank P=0.001). Combination CRAFITY score and AFP response at 6 weeks with AUROC predicts OS and tumor response to be 0.809 and 0.798, respectively, better than either CRAFITY score (0.771 & 0.750) or AFP response at 6 weeks (0.725 & 0.680) alone. In conclusions, the CAR classification which combining CRAFITY score and AFP response at 6 weeks provides a practical guidance for atezolizumab plus bevacizumab therapy in unresectable HCC patients.

摘要

阿替利珠单抗联合贝伐单抗的免疫检查点抑制剂是不可切除肝细胞癌(HCC)的有前景的治疗药物。我们尝试基于最近开发的CRAFITY评分并结合治疗期间甲胎蛋白(AFP)反应来指导治疗。纳入了89例接受阿替利珠单抗联合贝伐单抗治疗的不可切除HCC患者进行分析,无论其是否作为一线治疗。放射学评估基于改良的实体瘤疗效评价标准(mRECIST)。客观缓解率(ORR)和疾病控制率(DCR)分别为25.0%和65.5%。多变量分析显示,低CRAFITY评分(AFP<100 ng/ml或CRP<10 mg/l)以及6周时AFP反应良好(较基线下降≥75%或升高≤10%)是决定总生存期(OS)良好(风险比[HR]=0.143,P=0.002;HR=0.337,P=0.031)、无进展生存期(PFS)良好(HR=0.419,P=0.022;HR=0.429,P=0.025)以及反应良好(优势比[OR]=1.763,P=0.044;OR=3.881,P=0.011)的独立因素。根据CRAFITY评分与6周时AFP反应的组合将患者进一步分为三类[CAR(CRAFITY评分与AFP反应)分类]:6周时CRAFITY评分低且AFP反应良好(I类)、6周时CRAFITY评分高或AFP反应不佳(II类)以及6周时CRAFITY评分高且AFP反应不佳(III类)。I、II和III类患者的ORR分别为35.0%、18.2%和0%(总体P=0.034)。I类患者的OS和PFS最佳,其次是II类和III类(中位OS:未达到 vs. 11.1 vs. 4.3个月,对数秩检验P<0.001;中位PFS:7.9 vs. 6.6 vs. 2.6个月,对数秩检验P=0.001)。CRAFITY评分与6周时AFP反应联合的曲线下面积(AUROC)预测OS和肿瘤反应分别为0.809和0.798,优于单独的CRAFITY评分(0.771和0.750)或6周时的AFP反应(0.725和0.680)。总之,结合CRAFITY评分与6周时AFP反应的CAR分类为不可切除HCC患者的阿替利珠单抗联合贝伐单抗治疗提供了实用指导。

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