Therapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma
Abstract Aim To investigate the therapeutic effect of lenvatinib (LEN) in liver disease etiology, especially nonviral hepatocellular carcinoma (HCC). Methods and Results Sixty‐seven patients with unresectable advanced HCC (u‐HCC) treated with LEN and consisting of 26 hepatitis C virus (HCV), 19 hepa...
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Wiley
2021
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oai:doaj.org-article:db021b52981d4cb7841a5b454ff3109b2021-11-18T11:25:44ZTherapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma2397-907010.1002/jgh3.12663https://doaj.org/article/db021b52981d4cb7841a5b454ff3109b2021-11-01T00:00:00Zhttps://doi.org/10.1002/jgh3.12663https://doaj.org/toc/2397-9070Abstract Aim To investigate the therapeutic effect of lenvatinib (LEN) in liver disease etiology, especially nonviral hepatocellular carcinoma (HCC). Methods and Results Sixty‐seven patients with unresectable advanced HCC (u‐HCC) treated with LEN and consisting of 26 hepatitis C virus (HCV), 19 hepatitis B virus (HBV), 11 alcohol, and 11 nonalcoholic steatohepatitis (NASH) cases were retrospectively recruited. Univariate and multivariate Cox proportional hazard models were used to determine predictive factors for survival. The objective response rate in the nonviral (alcohol and NASH) group was higher than that in the viral group (59.1% [13/22] vs. 46.7% [21/45]). Progression‐free survival was significantly longer in the nonviral group than in the viral group (13.7 vs. 6.6 months; hazard ratio [HR] 0.324; 95% confidence interval [CI] 0.174–0.602; P < 0.01). Similarly, median overall survival (OS) was significantly longer in the nonviral group than in the viral group (not evaluable vs. 15.9 months; HR = 0.277; 95% CI = 0.116–0.662; P < 0.01). Multivariate analysis revealed that portal vein invasion (HR = 5.327, P = 0.0025), treatment line (HR = 0.455, P = 0.023), and etiology (HR = 0.180, P = 0.00055) were significant independent factors associated with OS in u‐HCC patients treated with LEN. Conclusion Our results suggest that LEN is more effective against nonviral u‐HCC than against viral u‐HCC.Tetsu TomonariYasushi SatoHironori TanakaTakeshi MitsuhashiAkihiro HiraoTakahiro TanakaTatsuya TaniguchiKoichi OkamotoMasahiro SogabeHiroshi MiyamotoNaoki MugurumaTetsuji TakayamaWileyarticleatezolizumabbevacizumablenvatinibDiseases of the digestive system. GastroenterologyRC799-869ENJGH Open, Vol 5, Iss 11, Pp 1275-1283 (2021) |
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atezolizumab bevacizumab lenvatinib Diseases of the digestive system. Gastroenterology RC799-869 |
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atezolizumab bevacizumab lenvatinib Diseases of the digestive system. Gastroenterology RC799-869 Tetsu Tomonari Yasushi Sato Hironori Tanaka Takeshi Mitsuhashi Akihiro Hirao Takahiro Tanaka Tatsuya Taniguchi Koichi Okamoto Masahiro Sogabe Hiroshi Miyamoto Naoki Muguruma Tetsuji Takayama Therapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma |
description |
Abstract Aim To investigate the therapeutic effect of lenvatinib (LEN) in liver disease etiology, especially nonviral hepatocellular carcinoma (HCC). Methods and Results Sixty‐seven patients with unresectable advanced HCC (u‐HCC) treated with LEN and consisting of 26 hepatitis C virus (HCV), 19 hepatitis B virus (HBV), 11 alcohol, and 11 nonalcoholic steatohepatitis (NASH) cases were retrospectively recruited. Univariate and multivariate Cox proportional hazard models were used to determine predictive factors for survival. The objective response rate in the nonviral (alcohol and NASH) group was higher than that in the viral group (59.1% [13/22] vs. 46.7% [21/45]). Progression‐free survival was significantly longer in the nonviral group than in the viral group (13.7 vs. 6.6 months; hazard ratio [HR] 0.324; 95% confidence interval [CI] 0.174–0.602; P < 0.01). Similarly, median overall survival (OS) was significantly longer in the nonviral group than in the viral group (not evaluable vs. 15.9 months; HR = 0.277; 95% CI = 0.116–0.662; P < 0.01). Multivariate analysis revealed that portal vein invasion (HR = 5.327, P = 0.0025), treatment line (HR = 0.455, P = 0.023), and etiology (HR = 0.180, P = 0.00055) were significant independent factors associated with OS in u‐HCC patients treated with LEN. Conclusion Our results suggest that LEN is more effective against nonviral u‐HCC than against viral u‐HCC. |
format |
article |
author |
Tetsu Tomonari Yasushi Sato Hironori Tanaka Takeshi Mitsuhashi Akihiro Hirao Takahiro Tanaka Tatsuya Taniguchi Koichi Okamoto Masahiro Sogabe Hiroshi Miyamoto Naoki Muguruma Tetsuji Takayama |
author_facet |
Tetsu Tomonari Yasushi Sato Hironori Tanaka Takeshi Mitsuhashi Akihiro Hirao Takahiro Tanaka Tatsuya Taniguchi Koichi Okamoto Masahiro Sogabe Hiroshi Miyamoto Naoki Muguruma Tetsuji Takayama |
author_sort |
Tetsu Tomonari |
title |
Therapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma |
title_short |
Therapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma |
title_full |
Therapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma |
title_fullStr |
Therapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma |
title_full_unstemmed |
Therapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma |
title_sort |
therapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma |
publisher |
Wiley |
publishDate |
2021 |
url |
https://doaj.org/article/db021b52981d4cb7841a5b454ff3109b |
work_keys_str_mv |
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