Literature DB >> 35530282

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

Wei Teng1,2, Chen-Chun Lin1,2, Chung-Wei Su1,2, Po-Ting Lin1,2, Yi-Chung Hsieh1,2, Wei-Ting Chen1,2, Ming-Mo Ho3,2, Ching-Ting Wang4,2, Pei-Mei Chai4,2, Jason Chia-Hsun Hsieh1,5,2, Chun-Yen Lin1,2, Shi-Ming Lin1,2.   

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. AJCR
Copyright © 2022.

Entities:  

Keywords:  CAR classification; atezolizumab plus bevacizumab; hepatocellular carcinoma; prognosis

Year:  2022        PMID: 35530282      PMCID: PMC9077079     

Source DB:  PubMed          Journal:  Am J Cancer Res        ISSN: 2156-6976            Impact factor:   5.942


  7 in total

1.  C-reactive protein and the acute phase response.

Authors:  M B Pepys
Journal:  Nature       Date:  1982-03-04       Impact factor: 49.962

2.  Association of preoperative serum CRP with PD-L1 expression in 508 patients with non-small cell lung cancer: A comprehensive analysis of systemic inflammatory markers.

Authors:  Takaki Akamine; Kazuki Takada; Gouji Toyokawa; Fumihiko Kinoshita; Taichi Matsubara; Yuka Kozuma; Naoki Haratake; Shinkichi Takamori; Fumihiko Hirai; Tetsuzo Tagawa; Tatsuro Okamoto; Yasuto Yoneshima; Isamu Okamoto; Mototsugu Shimokawa; Yoshinao Oda; Yoichi Nakanishi; Yoshihiko Maehara
Journal:  Surg Oncol       Date:  2018-01-09       Impact factor: 3.279

3.  Phase II trial of the combination of bevacizumab and erlotinib in patients who have advanced hepatocellular carcinoma.

Authors:  Melanie B Thomas; Jeffrey S Morris; Romil Chadha; Michiko Iwasaki; Harmeet Kaur; E Lin; Elinor Lin; Ahmed Kaseb; Katrina Glover; Marta Davila; James Abbruzzese
Journal:  J Clin Oncol       Date:  2009-01-12       Impact factor: 44.544

4.  Randomized phase II trial comparing bevacizumab plus carboplatin and paclitaxel with carboplatin and paclitaxel alone in previously untreated locally advanced or metastatic non-small-cell lung cancer.

Authors:  David H Johnson; Louis Fehrenbacher; William F Novotny; Roy S Herbst; John J Nemunaitis; David M Jablons; Corey J Langer; Russell F DeVore; Jacques Gaudreault; Lisa A Damico; Eric Holmgren; Fairooz Kabbinavar
Journal:  J Clin Oncol       Date:  2004-06-01       Impact factor: 44.544

5.  Phase II trial of bevacizumab and erlotinib as a second-line therapy for advanced hepatocellular carcinoma.

Authors:  Ahmed O Kaseb; Jeffrey S Morris; Michiko Iwasaki; Humaid O Al-Shamsi; Kanwal Pratap Singh Raghav; Lauren Girard; Sheree Cheung; Van Nguyen; Khaled M Elsayes; Lianchun Xiao; Reham Abdel-Wahab; Ahmed S Shalaby; Manal Hassan; Hesham M Hassabo; Robert A Wolff; James C Yao
Journal:  Onco Targets Ther       Date:  2016-02-15       Impact factor: 4.147

6.  Association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma.

Authors:  Bruno Sangro; Ignacio Melero; Samir Wadhawan; Richard S Finn; Ghassan K Abou-Alfa; Ann-Lii Cheng; Thomas Yau; Junji Furuse; Joong-Won Park; Zachary Boyd; Hao Tracy Tang; Yun Shen; Marina Tschaika; Jaclyn Neely; Anthony El-Khoueiry
Journal:  J Hepatol       Date:  2020-07-22       Impact factor: 25.083

7.  C-Reactive Protein Impairs Dendritic Cell Development, Maturation, and Function: Implications for Peripheral Tolerance.

Authors:  Rachel V Jimenez; Tyler T Wright; Nicholas R Jones; Jianming Wu; Andrew W Gibson; Alexander J Szalai
Journal:  Front Immunol       Date:  2018-03-05       Impact factor: 7.561

  7 in total
  1 in total

Review 1.  Non-Invasive Biomarkers for Immunotherapy in Patients with Hepatocellular Carcinoma: Current Knowledge and Future Perspectives.

Authors:  Maria Pallozzi; Natalia Di Tommaso; Valeria Maccauro; Francesco Santopaolo; Antonio Gasbarrini; Francesca Romana Ponziani; Maurizio Pompili
Journal:  Cancers (Basel)       Date:  2022-09-23       Impact factor: 6.575

  1 in total

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