Tislelizumab in patients with previously treated advanced hepatocellular carcinoma (RATIONALE-208): A multicenter, non-randomized, open-label, phase 2 trial Journal Article


Authors: Ren, Z.; Ducreux, M.; Abou-Alfa, G. K.; Merle, P.; Fang, W.; Edeline, J.; Li, Z.; Wu, L.; Assenat, E.; Hu, S.; Rimassa, L.; Zhang, T.; Blanc, J. F.; Pan, H.; Ross, P.; Yen, C. J.; Tran, A.; Shao, G.; Bouattour, M.; Chen, Y.; Meyer, T.; Hou, J.; Tougeron, D.; Bai, Y.; Hou, M. M.; Meng, Z.; Wu, J.; Li, V.; Chica-Duque, S.; Cheng, A. L.
Article Title: Tislelizumab in patients with previously treated advanced hepatocellular carcinoma (RATIONALE-208): A multicenter, non-randomized, open-label, phase 2 trial
Abstract: Introduction: Tislelizumab (anti-programmed cell death protein 1 antibody) showed preliminary antitumor activity and tolerability in patients with advanced solid tumors, including hepatocellular carcinoma (HCC). This study aimed to assess the efficacy and safety of tislelizumab in patients with previously treated advanced HCC. Methods: The multiregional phase 2 study RATIONALE-208 examined single-agent tislelizumab (200 mg intravenously every 3 weeks) in patients with advanced HCC with Child-Pugh A, Barcelona Clinic Liver Cancer stage B or C, and who had received one or more prior lines of systemic therapy. The primary endpoint was objective response rate (ORR), radiologically confirmed per Response Evaluation Criteria in Solid Tumors version 1.1 by the Independent Review Committee. Safety was assessed in patients who received ≥1 dose of tislelizumab. Results: Between April 9, 2018, and February 27, 2019, 249 eligible patients were enrolled and treated. After a median study follow-up of 12.7 months, ORR was 13% (n = 32/249; 95% confidence interval [CI], 9-18), including five complete and 27 partial responses. The number of prior lines of therapy did not impact ORR (one prior line, 13% [95% CI, 8-20]; two or more prior lines, 13% [95% CI, 7-20]). Median duration of response was not reached. The disease control rate was 53%, and median overall survival was 13.2 months. Of the 249 total patients, grade ≥3 treatment-related adverse events were reported in 38 (15%) patients; the most common was liver transaminase elevations in 10 (4%) patients. Treatment-related adverse events led to treatment discontinuation in 13 (5%) patients or dose delay in 46 (19%) patients. No deaths were attributed to the treatment per investigator assessment. Conclusion: Tislelizumab demonstrated durable objective responses, regardless of the number of prior lines of therapy, and acceptable tolerability in patients with previously treated advanced HCC. © 2022 Authors
Keywords: hepatocellular carcinoma; immunotherapy; tislelizumab; pretreated patient population
Journal Title: Liver Cancer
Volume: 12
Issue: 1
ISSN: 2235-1795
Publisher: Karger  
Date Published: 2023-02-01
Start Page: 72
End Page: 84
Language: English
DOI: 10.1159/000527175
PROVIDER: scopus
PMCID: PMC9982342
PUBMED: 36872927
DOI/URL:
Notes: Article -- MSK corresponding author is Ghassan Abou-Alfa -- Source: Scopus
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  1. Ghassan Abou-Alfa
    576 Abou-Alfa