Literature DB >> 31019903

Surrogacy of Time to Progression for Overall Survival in Advanced Hepatocellular Carcinoma Treated with Systemic Therapy: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Takeshi Terashima1, Tatsuya Yamashita1, Tadashi Toyama2, Kuniaki Arai1, Kazunori Kawaguchi1, Kazuya Kitamura1, Taro Yamashita1, Yoshio Sakai1, Eishiro Mizukoshi1, Masao Honda1, Shuichi Kaneko1.   

Abstract

Time to progression (TTP) is widely used as the endpoint in early-phase trials of advanced hepatocellular carcinoma (HCC). However, the relevance of using TTP as a surrogate marker for overall survival (OS) in pivotal trials remains uncertain. The PubMed database and ASCO Meeting Library were searched for reports of randomized controlled trials that investigated patients with advanced HCC, included data for both OS and TTP, and were launched between 2009 and 2016. The correlation between hazard ratios (HRs) for TTP and OS was determined using weighted linear regression. Correlations between median OS and TTP, and between median OS and postprogression survival (PPS), defined as the period obtained by subtracting the median TTP from the median OS, were also evaluated. The database search yielded 24 trials with 50 arms. Overall, TTP HR correlated with OS HR (R = 0.73); however, the coefficient in the regression equation was 0.48. The correlation between median OS and median TTP was not so strong (R = 0.50), whereas the correlation between median OS and median PPS was strong (R = 0.78). In advanced HCC, the OS HR can be predicted from the TTP HR, which is useful when considering whether to proceed to a pivotal trial based on the results of early-phase trials. TTP may be a better endpoint than OS for evaluating a novel agent in a pivotal trial, because an improvement in antitumor effect cannot fully reflect an improvement in OS due to the strong impact of PPS on OS.

Entities:  

Keywords:  Clinical trials; Hepatocellular carcinoma; Molecular targeted therapy; Overall survival; Surrogate endpoint; Time to progression

Year:  2018        PMID: 31019903      PMCID: PMC6465721          DOI: 10.1159/000489505

Source DB:  PubMed          Journal:  Liver Cancer        ISSN: 1664-5553            Impact factor:   11.740


  30 in total

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7.  Efficacy and safety of sorafenib in patients in the Asia-Pacific region with advanced hepatocellular carcinoma: a phase III randomised, double-blind, placebo-controlled trial.

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Journal:  J Natl Cancer Inst       Date:  2008-05-13       Impact factor: 13.506

9.  Sorafenib in advanced hepatocellular carcinoma.

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Journal:  N Engl J Med       Date:  2008-07-24       Impact factor: 91.245

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Journal:  Eur J Cancer       Date:  2009-03-19       Impact factor: 9.162

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Journal:  Liver Cancer       Date:  2021-12-06       Impact factor: 11.740

3.  Comparative study between sorafenib and lenvatinib as the first-line therapy in the sequential treatment of unresectable hepatocellular carcinoma in a real-world setting.

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Journal:  JGH Open       Date:  2021-12-17

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