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

被引:1
作者
Teng, Wei [1 ,5 ]
Lin, Chen-Chun [1 ,5 ]
Su, Chung-Wei [1 ,5 ]
Lin, Po-Ting [1 ,5 ]
Hsieh, Yi-Chung [1 ,5 ]
Chen, Wei-Ting [1 ,5 ]
Ho, Ming-Mo [2 ,5 ]
Wang, Ching-Ting [4 ,5 ]
Chai, Pei-Mei [4 ,5 ]
Hsieh, Jason Chia-Hsun [1 ,3 ,5 ]
Lin, Chun-Yen [1 ,5 ]
Lin, Shi-Ming [1 ,5 ]
机构
[1] Chang Gung Mem Hosp, Linkou Med Ctr, Dept Gastroenterol & Hepatol, Taoyuan, Taiwan
[2] Chang Gung Mem Hosp, Linkou Med Ctr, Dept Med Oncol, Taoyuan, Taiwan
[3] New Taipei Municipal City Tucheng Hosp, Dept Internal Med, Div Hematol Oncol, New Taipei, Taiwan
[4] Chang Gung Mem Hosp, Dept Nursing, Linkou Med Ctr, Taoyuan, Taiwan
[5] Chang Gung Univ, Coll Med, Taoyuan, Taiwan
关键词
CAR classification; hepatocellular carcinoma; atezolizumab plus bevacizumab; prognosis; C-REACTIVE PROTEIN; SURVIVAL; PEMBROLIZUMAB; MATURATION; EFFICACY; THERAPY; STAGE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:1899 / +
页数:15
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