Immune Checkpoint Inhibitors for Child-Pugh Class B Advanced Hepatocellular Carcinoma

Author:

Xie Enrui1,Yeo Yee Hui2,Scheiner Bernhard34,Zhang Yue15,Hiraoka Atsushi6,Tantai Xinxing7,Fessas Petros3,de Castro Tiago8,D’Alessio Antonio3,Fulgenzi Claudia Angela Maria3,Xu Shuo9,Tsai Hong-Ming10,Kambhampati Swetha11,Wang Wenjun1,Keenan Bridget P.12,Gao Xu17,Xing Zixuan1,Pinter Matthias4,Lin Yih-Jyh13,Guo Zhanjun9,Vogel Arndt8,Tanaka Takaaki6,Kuo Hsin-Yu1415,Kelley Robin K.12,Kudo Masatoshi16,Yang Ju Dong217,Pinato David J.318,Ji Fanpu1192021

Affiliation:

1. Department of Infectious Diseases, The Second Affiliated Hospital of Xi’an Jiaotong University, Xi’an, China

2. Karsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California

3. Department of Surgery and Cancer, Imperial College London, United Kingdom

4. Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Austria

5. The Eighth Hospital of Xi’an City, Xi’an Jiaotong University, Shaanxi, China

6. Gastroenterology Center, Ehime Prefectural Central Hospital, Matsuyama, Japan

7. Department of Gastroenterology, The Second Affiliated Hospital of Xi’an Jiaotong University, Xi’an, China

8. Department of Gastroenterology, Hepatology, Infectious Diseases and Endocrinology, Hannover Medical School, Hannover, Germany

9. Department of Rheumatology and Immunology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China

10. Department of Diagnostic Radiology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan

11. Department of Hematology and Hematopoietic Stem Cell Transplantation, City of Hope National Medical Center, Duarte, California

12. Division of Hematology/Oncology, Department of Medicine, Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco

13. Department of Surgery, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan

14. Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan

15. Institute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan

16. Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka, Japan

17. Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California

18. Division of Oncology, Department of Translational Medicine, University of Piemonte Orientale “A Avogadro,” Novara, Italy

19. National and Local Joint Engineering Research Center of Biodiagnosis and Biotherapy, The Second Affiliated Hospital of Xi’an Jiaotong University, Xi’an, China

20. Shaanxi Provincial Clinical Medical Research Center of Infectious Diseases, Xi’an, China

21. Key Laboratory of Surgical Critical Care and Life Support (Xi’an Jiaotong University), Ministry of Education, Xi’an, China

Abstract

ImportanceImmune checkpoint inhibitors (ICIs) are increasingly used in patients with advanced hepatocellular carcinoma (HCC). However, data on ICI therapy in patients with advanced HCC and impaired liver function are scarce.ObjectiveTo conduct a systematic review and meta-analysis to determine the efficacy and safety of ICI treatment for advanced HCC with Child-Pugh B liver function.Data SourcesPubMed, Embase, Web of Science, and Cochrane Library were searched for relevant studies from inception through June 15, 2022.Study SelectionRandomized clinical trials, cohort studies, or single-group studies that investigated the efficacy or safety of ICI therapy for Child-Pugh B advanced HCC were included.Data Extraction and SynthesisThe Preferred Reporting Items for Systematic Reviews and Meta-Analysis guideline was followed to extract data. A random-effects model was adopted if the heterogeneity was significant (I2 > 50%); otherwise, a fixed-effect model was used.Main Outcomes and MeasuresThe objective response rate (ORR) and overall survival (OS) were considered to be the primary efficacy outcomes of ICI treatment for Child-Pugh B advanced HCC, and the incidence of treatment-related adverse events (trAEs) was set as the primary measure for the safety outcome.ResultsA total of 22 studies including 699 patients with Child-Pugh B and 2114 with Child-Pugh A advanced HCC comprised the analytic sample (median age range, 53-73 years). Upon pooled analysis, patients treated with ICIs in the Child-Pugh B group had an ORR of 14% (95% CI, 11%-17%) and disease control rate (DCR) of 46% (95% CI, 36%-56%), with a median OS of 5.49 (95% CI, 3.57-7.42) months and median progression-free survival of 2.68 (95% CI, 1.85-3.52) months. The rate of any grade trAEs in the Child-Pugh B group was 40% (95% CI, 34%-47%) and of grade 3 or higher trAEs was 12% (95% CI, 6%-23%). Compared with the Child-Pugh A group, the ORR (odds ratio, 0.59; 95% CI, 0.43-0.81; P < .001) and DCR (odds ratio, 0.64; 95% CI, 0.50-0.81; P < .001) were lower in the Child-Pugh B group. Child-Pugh B was independently associated with worse OS in patients with advanced HCC treated with ICIs (hazard ratio, 2.72 [95% CI, 2.34-3.16]; adjusted hazard ratio, 2.33 [95% CI, 1.81-2.99]). However, ICIs were not associated with increased trAEs in the Child-Pugh B group.Conclusions and RelevanceThe findings of this systematic review and meta-analysis suggest that although the safety of ICI treatment was comparable between patients with HCC with vs without advanced liver disease and the treatment resulted in a significant number of radiologic responses, survival outcomes are still inferior in patients with worse liver function. More study is needed to determine the effectiveness of ICI treatment in this population.

Publisher

American Medical Association (AMA)

Subject

Oncology,Cancer Research

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