Therapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma. Issue 11 (22nd October 2021)
- Record Type:
- Journal Article
- Title:
- Therapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma. Issue 11 (22nd October 2021)
- Main Title:
- Therapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma
- Authors:
- Tomonari, Tetsu
Sato, Yasushi
Tanaka, Hironori
Mitsuhashi, Takeshi
Hirao, Akihiro
Tanaka, Takahiro
Taniguchi, Tatsuya
Okamoto, Koichi
Sogabe, Masahiro
Miyamoto, Hiroshi
Muguruma, Naoki
Takayama, Tetsuji - Abstract:
- 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. Abstract : Kaplan–Meier analysis of progression‐free survival amongAbstract: 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. Abstract : Kaplan–Meier analysis of progression‐free survival among patients with unresectable advanced hepatocellular carcinoma treated with lenvatinib according to etiology. The PFS in the non‐viral group was significantly longer than that in the viral group. Our results suggest that LEN is more effective against non‐viral u‐HCC than against viral u‐HCC. … (more)
- Is Part Of:
- JGH open. Volume 5:Issue 11(2021)
- Journal:
- JGH open
- Issue:
- Volume 5:Issue 11(2021)
- Issue Display:
- Volume 5, Issue 11 (2021)
- Year:
- 2021
- Volume:
- 5
- Issue:
- 11
- Issue Sort Value:
- 2021-0005-0011-0000
- Page Start:
- 1275
- Page End:
- 1283
- Publication Date:
- 2021-10-22
- Subjects:
- atezolizumab -- bevacizumab -- lenvatinib
- Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/jgh3.12663 ↗
- Languages:
- English
- ISSNs:
- 2397-9070
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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- 19853.xml