Literature DB >> 30574480

Survival of Hepatocellular Carcinoma Patients Treated with Sorafenib beyond Progression.

Leonidas Apostolidis1,2, Jan Pfeiffenberger3,2, Daniel Gotthardt3,2, Boris Radeleff4,2, Arianeb Mehrabi5,2, Peter Schemmer5,6,2, Dirk Jäger1,2, Peter Schirmacher7,2, Wolfgang Stremmel3,2, Henning Schulze-Bergkamen1,8,2, Christoph Springfeld1,2, Karl Heinz Weiss3,2.   

Abstract

BACKGROUND/AIM: Sorafenib leads to improved survival in advanced hepatocellular carcinoma (HCC) patients. Continuation of sorafenib beyond progression has been a possible treatment strategy when further approved therapeutic agents are lacking.
METHODS: We performed a retrospective analysis of all HCC patients at our institution with documented disease progression under treatment with sorafenib. Overall survival (OS) from start of sorafenib treatment was compared between patients who received sorafenib for > 3 weeks beyond progression (group 1) and those who discontinued sorafenib ≤3 weeks after progression (group 2). Group 1 was further subdivided into those patients who received sorafenib for > 3 months (group 1a) and those who received it for ≤3 months (group 1b).
RESULTS: A total of 71 patients were analyzed. Median OS for all patients was 15.4 months. OS in group 1 (15.6 months) and 2 (13.0 months) was similar (p = 0.90). Patients in group 1a showed significantly prolonged median OS (19.7 months) compared to that of patients in group 1b (13.6 months, p = 0.004), and they showed a trend towards prolonged OS compared to group 2 (p = 0.126). For patients with a poor prognosis according to their Child-Pugh stage, performance status, alpha-fetoprotein, and response to prior sorafenib treatment, OS was significantly prolonged in group 1 versus group 2 (12.1 vs. 6.4 months, p = 0.019).
CONCLUSION: In HCC patients, continuing sorafenib beyond progression for > 3 months is associated with improved survival compared to discontinuing sorafenib within 3 months. Furthermore, patients with a poor prognosis who continue sorafenib beyond progression in general show significantly prolonged survival.

Entities:  

Keywords:  Hepatocellular carcinoma; Molecular-targeted therapies; Progression; Sorafenib; Survival; Therapeutics; Therapy; Treatment

Year:  2018        PMID: 30574480      PMCID: PMC6288626          DOI: 10.1159/000487635

Source DB:  PubMed          Journal:  Gastrointest Tumors        ISSN: 2296-3774


  20 in total

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Journal:  Hepatology       Date:  2005-11       Impact factor: 17.425

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3.  Continuation of bevacizumab after first progression in metastatic colorectal cancer (ML18147): a randomised phase 3 trial.

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Journal:  Lancet Oncol       Date:  2012-11-16       Impact factor: 41.316

4.  Disease flare after tyrosine kinase inhibitor discontinuation in patients with EGFR-mutant lung cancer and acquired resistance to erlotinib or gefitinib: implications for clinical trial design.

Authors:  Jamie E Chaft; Geoffrey R Oxnard; Camelia S Sima; Mark G Kris; Vincent A Miller; Gregory J Riely
Journal:  Clin Cancer Res       Date:  2011-08-19       Impact factor: 12.531

5.  Bevacizumab beyond first progression is associated with prolonged overall survival in metastatic colorectal cancer: results from a large observational cohort study (BRiTE).

Authors:  Axel Grothey; Mary M Sugrue; David M Purdie; Wei Dong; Daniel Sargent; Eric Hedrick; Mark Kozloff
Journal:  J Clin Oncol       Date:  2008-10-14       Impact factor: 44.544

6.  Clinical modes of EGFR tyrosine kinase inhibitor failure and subsequent management in advanced non-small cell lung cancer.

Authors:  Jin-Ji Yang; Hua-Jun Chen; Hong-Hong Yan; Xu-Chao Zhang; Qing Zhou; Jian Su; Zhen Wang; Chong-Rui Xu; Yi-Sheng Huang; Bin-Chao Wang; Xue-Ning Yang; Wen-Zhao Zhong; Qiang Nie; Ri-Qiang Liao; Ben-Yuan Jiang; Song Dong; Yi-Long Wu
Journal:  Lung Cancer       Date:  2012-10-15       Impact factor: 5.705

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.

Authors:  Ann-Lii Cheng; Yoon-Koo Kang; Zhendong Chen; Chao-Jung Tsao; Shukui Qin; Jun Suk Kim; Rongcheng Luo; Jifeng Feng; Shenglong Ye; Tsai-Sheng Yang; Jianming Xu; Yan Sun; Houjie Liang; Jiwei Liu; Jiejun Wang; Won Young Tak; Hongming Pan; Karin Burock; Jessie Zou; Dimitris Voliotis; Zhongzhen Guan
Journal:  Lancet Oncol       Date:  2008-12-16       Impact factor: 41.316

8.  Sorafenib in advanced hepatocellular carcinoma.

Authors:  Josep M Llovet; Sergio Ricci; Vincenzo Mazzaferro; Philip Hilgard; Edward Gane; Jean-Frédéric Blanc; Andre Cosme de Oliveira; Armando Santoro; Jean-Luc Raoul; Alejandro Forner; Myron Schwartz; Camillo Porta; Stefan Zeuzem; Luigi Bolondi; Tim F Greten; Peter R Galle; Jean-François Seitz; Ivan Borbath; Dieter Häussinger; Tom Giannaris; Minghua Shan; Marius Moscovici; Dimitris Voliotis; Jordi Bruix
Journal:  N Engl J Med       Date:  2008-07-24       Impact factor: 91.245

9.  Clinical course of sorafenib treatment in patients with hepatocellular carcinoma.

Authors:  Hyun Young Woo; Jeong Heo; Ki Tae Yoon; Gwang Ha Kim; Dae Hwan Kang; Geun Am Song; Mong Cho
Journal:  Scand J Gastroenterol       Date:  2012-05-08       Impact factor: 2.423

10.  Tivantinib for second-line treatment of advanced hepatocellular carcinoma: a randomised, placebo-controlled phase 2 study.

Authors:  Armando Santoro; Lorenza Rimassa; Ivan Borbath; Bruno Daniele; Stefania Salvagni; Jean Luc Van Laethem; Hans Van Vlierberghe; Jörg Trojan; Frank T Kolligs; Alan Weiss; Steven Miles; Antonio Gasbarrini; Monica Lencioni; Luca Cicalese; Morris Sherman; Cesare Gridelli; Peter Buggisch; Guido Gerken; Roland M Schmid; Corrado Boni; Nicola Personeni; Ziad Hassoun; Giovanni Abbadessa; Brian Schwartz; Reinhard Von Roemeling; Maria E Lamar; Yinpu Chen; Camillo Porta
Journal:  Lancet Oncol       Date:  2012-11-20       Impact factor: 41.316

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