Camrelizumab in patients with previously treated advanced hepatocellular carcinoma: a multicentre, open-label, parallel-group, randomised, phase 2 trial
- PMID: 32112738
- DOI: 10.1016/S1470-2045(20)30011-5
Camrelizumab in patients with previously treated advanced hepatocellular carcinoma: a multicentre, open-label, parallel-group, randomised, phase 2 trial
Abstract
Background: Blocking the interaction between PD-1 and its ligands is a promising treatment strategy for advanced hepatocellular carcinoma. This study aimed to assess the antitumour activity and safety of the anti-PD-1 inhibitor camrelizumab in pretreated patients with advanced hepatocellular carcinoma.
Methods: This is a multicentre, open-label, parallel-group, randomised, phase 2 trial done at 13 study sites in China. Eligible patients were aged 18 years and older with a histological or cytological diagnosis of advanced hepatocellular carcinoma, had progressed on or were intolerant to previous systemic treatment, and had an Eastern Cooperative Oncology Group performance score of 0-1. Patients were randomly assigned (1:1) to receive camrelizumab 3 mg/kg intravenously every 2 or 3 weeks, via a centralised interactive web-response system using block randomisation (block size of four). The primary endpoints were objective response (per blinded independent central review) and 6-month overall survival, in all randomly assigned patients who had at least one dose of study treatment. Safety was analysed in all treated patients. This study is registered with ClinicalTrials.gov, number NCT02989922, and follow-up is ongoing, but enrolment is closed.
Findings: Between Nov 15, 2016, and Nov 16, 2017, 303 patients were screened for eligibility, of whom 220 eligible patients were randomly assigned and among whom 217 received camrelizumab (109 patients were given treatment every 2 weeks and 108 every 3 weeks). Median follow-up was 12·5 months (IQR 5·7-15·5). Objective response was reported in 32 (14·7%; 95% CI 10·3-20·2) of 217 patients. The overall survival probability at 6 months was 74·4% (95% CI 68·0-79·7)]. Grade 3 or 4 treatment-related adverse events occurred in 47 (22%) of 217 patients; the most common were increased aspartate aminotransferase (ten [5%]) and decreased neutrophil count (seven [3%]). Two deaths were judged by the investigators to be potentially treatment-related (one due to liver dysfunction and one due to multiple organ failure).
Interpretation: Camrelizumab showed antitumour activity in pretreated Chinese patients with advanced hepatocellular carcinoma, with manageable toxicities, and might represent a new treatment option for these patients.
Funding: Jiangsu Hengrui Medicine.
Copyright © 2020 Elsevier Ltd. All rights reserved.
Comment in
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Effectiveness of anti-PD-1 for hepatocellular carcinoma.Lancet Oncol. 2020 Jun;21(6):e293. doi: 10.1016/S1470-2045(20)30170-4. Lancet Oncol. 2020. PMID: 32502446 No abstract available.
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Effectiveness of anti-PD-1 for hepatocellular carcinoma - Authors' reply.Lancet Oncol. 2020 Jun;21(6):e294. doi: 10.1016/S1470-2045(20)30285-0. Lancet Oncol. 2020. PMID: 32502447 No abstract available.
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A large randomized clinical trial is necessary to establish the role of camrelizumab in hepatocellular carcinoma.Ann Transl Med. 2020 Oct;8(19):1253. doi: 10.21037/atm-2020-71. Ann Transl Med. 2020. PMID: 33178785 Free PMC article. No abstract available.
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Camrelizumab-targeting a novel PD-1 epitope to treat hepatocellular carcinoma.Ann Transl Med. 2020 Dec;8(23):1614. doi: 10.21037/atm-2020-115. Ann Transl Med. 2020. PMID: 33437813 Free PMC article. No abstract available.
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Anti-PD1 monotherapy in hepatocellular carcinoma: a step forward or already behind?Ann Transl Med. 2020 Dec;8(24):1701. doi: 10.21037/atm-20-4438. Ann Transl Med. 2020. PMID: 33490213 Free PMC article. No abstract available.
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Combination strategies in advanced hepatocellular carcinoma: the CARES-310 trial.Lancet. 2024 Oct 12;404(10461):1404-1405. doi: 10.1016/S0140-6736(24)01771-9. Lancet. 2024. PMID: 39396345 No abstract available.
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