Literature DB >> 12372045

Hepatocellular carcinoma: strategy for optimizing surgical resection, transplantation and palliation.

Robert A Fisher1, Timothy P Maroney, Ann S Fulcher, Daniel Maluf, John A Clay, Luke G Wolfe, Sherfield Dawson, Adrian Cotterell, R Todd Stravitz, Velimir A Luketic, Mitchell Shiffman, Richard K Sterling, Marc P Posner.   

Abstract

In December 1997, a prospective study with informed consent was initiated to test a neoadjuvant treatment of transcatheter hepatic arterial chemo-embolization (TACE) and thermal or chemical ablation followed by transcatheter hepatic arterial chemo-infusion (TACI) in patients with hepatocellular carcinoma (HCC) referred for transplantation (OLT) and for resection. Patients were staged with American Liver Tumor Study Group-modified tumour-node-metastasis (TNM) staging classification using serial 3-6 month physical exam, alphafetoprotein (AFP), abdominal enhanced MRI, chest CT and bone scan. Sixty-five patients with HCC, out of 508 patients referred for OLT, were divided into five clinical groups and an incidental HCC patient group (n = 8), diagnosed on post-transplant explant pathology. The key focus of study was safety, site of HCC recurrence and tumour free survival. One hundred and thirty three ablation, infusion procedures were performed with an overall 24.8% morbidity, including two septic deaths. There were 13 (21.6%) HCC recurrences in 60 patients having one or more ablative treatments with only 23% hepatic HCC recurrences at 43 months of study. Eighteen HCC patients were listed for OLT (Group 3), with 12 patients transplanted after 29-424 d waiting. Two patients were removed from the OLT list due to HCC metastases, waiting a mean of 145 d. Two patients, post-OLT, had their TNM score upgraded from T2, T3 to T4. No Group 3 post-OLT patient has died or had HCC recurrence at mean follow-up of 27 +/- 15 months. No incidental HCC group post-OLT patient has died or had HCC recurrence at mean follow-up of 24 +/- 14 months. This neoadjuvant protocol is safe and effective in reducing HCC recurrence prior to and after OLT and resection.

Entities:  

Mesh:

Year:  2002        PMID: 12372045     DOI: 10.1034/j.1399-0012.16.s7.8.x

Source DB:  PubMed          Journal:  Clin Transplant        ISSN: 0902-0063            Impact factor:   2.863


  4 in total

1.  Lentivirally engineered dendritic cells activate AFP-specific T cells which inhibit hepatocellular carcinoma growth in vitro and in vivo.

Authors:  Yang Liu; Lisa H Butterfield; Xiaohui Fu; Zhenshun Song; Xiaoping Zhang; Chongde Lu; Guanghui Ding; Mengchao Wu
Journal:  Int J Oncol       Date:  2011-04-13       Impact factor: 5.650

2.  Differentially expressed genes between early and advanced hepatocellular carcinoma (HCC) as a potential tool for selecting liver transplant recipients.

Authors:  Valeria R Mas; Daniel G Maluf; Kellie J Archer; Kenneth Yanek; Bridgette Williams; Robert A Fisher
Journal:  Mol Med       Date:  2006 Apr-Jun       Impact factor: 6.354

3.  Resection prior to liver transplantation for hepatocellular carcinoma.

Authors:  Jacques Belghiti; Alexandre Cortes; Eddie K Abdalla; Jean-Marc Régimbeau; Kurumboor Prakash; François Durand; Daniele Sommacale; Federica Dondero; Mickael Lesurtel; Alain Sauvanet; Olivier Farges; Reza Kianmanesh
Journal:  Ann Surg       Date:  2003-12       Impact factor: 12.969

4.  The expression of embryonic liver development genes in hepatitis C induced cirrhosis and hepatocellular carcinoma.

Authors:  Martha Behnke; Mark Reimers; Robert Fisher
Journal:  Cancers (Basel)       Date:  2012-09-01       Impact factor: 6.639

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.