Literature DB >> 34108184

Pharmacodynamic Biomarkers Predictive of Survival Benefit with Lenvatinib in Unresectable Hepatocellular Carcinoma: From the Phase III REFLECT Study.

Richard S Finn1, Masatoshi Kudo2, Ann-Lii Cheng3, Lucjan Wyrwicz4, Roger K C Ngan5, Jean-Frederic Blanc6, Ari D Baron7, Arndt Vogel8, Masafumi Ikeda9, Fabio Piscaglia10, Kwang-Hyub Han11, Shukui Qin12, Yukinori Minoshima13, Michio Kanekiyo14, Min Ren14, Ryo Dairiki13, Toshiyuki Tamai15, Corina E Dutcus14, Hiroki Ikezawa15, Yasuhiro Funahashi13, Thomas R Jeffry Evans16.   

Abstract

PURPOSE: In REFLECT, lenvatinib demonstrated an effect on overall survival (OS) by confirmation of noninferiority to sorafenib in unresectable hepatocellular carcinoma. This analysis assessed correlations between serum or tissue biomarkers and efficacy outcomes from REFLECT. EXPERIMENTAL
DESIGN: Serum biomarkers (VEGF, ANG2, FGF19, FGF21, and FGF23) were measured by ELISA. Gene expression in tumor tissues was measured by the nCounter PanCancer Pathways Panel. Pharmacodynamic changes in serum biomarker levels from baseline, and associations of clinical outcomes with baseline biomarker levels, were evaluated.
RESULTS: Four hundred and seven patients were included in the serum analysis set (lenvatinib n = 279, sorafenib n = 128); 58 patients were included in the gene-expression analysis set (lenvatinib n = 34, sorafenib n = 24). Both treatments were associated with increases in VEGF; only lenvatinib was associated with increases in FGF19 and FGF23 at all time points. Lenvatinib-treated responders had greater increases in FGF19 and FGF23 versus nonresponders at cycle 4, day 1 (FGF19: 55.2% vs. 18.3%, P = 0.014; FGF23: 48.4% vs. 16.4%, P = 0.0022, respectively). Higher baseline VEGF, ANG2, and FGF21 correlated with shorter OS in both treatment groups. OS was longer for lenvatinib than sorafenib [median, 10.9 vs. 6.8 months, respectively; HR, 0.53; 95% confidence interval (CI), 0.33-0.85; P-interaction = 0.0397] with higher baseline FGF21. In tumor tissue biomarker analysis, VEGF/FGF-enriched groups showed improved OS with lenvatinib versus the intermediate VEGF/FGF group (HR, 0.39; 95% CI, 0.16-0.91; P = 0.0253).
CONCLUSIONS: Higher baseline levels of VEGF, FGF21, and ANG2 may be prognostic for shorter OS. Higher baseline FGF21 may be predictive for longer OS with lenvatinib compared with sorafenib, but this needs confirmation. ©2021 The Authors; Published by the American Association for Cancer Research.

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Year:  2021        PMID: 34108184     DOI: 10.1158/1078-0432.CCR-20-4219

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  7 in total

1.  p53 m6A modulation sensitizes hepatocellular carcinoma to apatinib through apoptosis.

Authors:  Weiwei Ke; Linlin Zhang; Xiangxuan Zhao; Zaiming Lu
Journal:  Apoptosis       Date:  2022-05-03       Impact factor: 4.677

2.  Advanced hepatocellular carcinoma treated by transcatheter arterial chemoembolization with drug-eluting beads plus lenvatinib versus sorafenib, a propensity score matching retrospective study.

Authors:  Miao Xue; Yanqin Wu; Bowen Zhu; Xinhua Zou; Wenzhe Fan; Jiaping Li
Journal:  Am J Cancer Res       Date:  2021-12-15       Impact factor: 6.166

3.  The change rate in serum nitric oxide may affect lenvatinib therapy in hepatocellular carcinoma.

Authors:  Atsushi Kawamura; Haruki Uojima; Makoto Chuma; Xue Shao; Hisashi Hidaka; Takahide Nakazawa; Akira Take; Yoshihiko Sakaguchi; Kazushi Numata; Makoto Kako; Akito Nozaki; Shintaro Azuma; Kazue Horio; Chika Kusano; Koichiro Atsuda
Journal:  BMC Cancer       Date:  2022-08-23       Impact factor: 4.638

Review 4.  Assessment and Monitoring of Response to Systemic Treatment in Advanced Hepatocellular Carcinoma: Current Insights.

Authors:  Nicola Personeni; Lorenza Rimassa; Antonella Cammarota; Valentina Zanuso; Tiziana Pressiani
Journal:  J Hepatocell Carcinoma       Date:  2022-09-14

Review 5.  Neoadjuvant Therapy for Hepatocellular Carcinoma.

Authors:  Zongyi Yin; Dongying Chen; Shuang Liang; Xiaowu Li
Journal:  J Hepatocell Carcinoma       Date:  2022-08-31

Review 6.  Lenvatinib plus transarterial chemoembolization with or without immune checkpoint inhibitors for unresectable hepatocellular carcinoma: A review.

Authors:  Liwei Sun; Xuelong Xu; Fanguang Meng; Qian Liu; Hankang Wang; Xiaodong Li; Guijie Li; Feng Chen
Journal:  Front Oncol       Date:  2022-09-28       Impact factor: 5.738

Review 7.  Is There Still a Place for Tyrosine Kinase Inhibitors for the Treatment of Hepatocellular Carcinoma at the Time of Immunotherapies? A Focus on Lenvatinib.

Authors:  Marie Decraecker; Caroline Toulouse; Jean-Frédéric Blanc
Journal:  Cancers (Basel)       Date:  2021-12-16       Impact factor: 6.639

  7 in total

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