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Multidisciplinary Management of Hepatocellular Carcinoma in Clinical Practice
Background. Hepatocellular carcinoma (HCC) patients require different treatment strategies according to disease extension, liver function, and patient's fitness. We evaluated HCC multidisciplinary management in clinical practice. Methods. Consecutive patients were followed and treated with tail...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4034404/ https://www.ncbi.nlm.nih.gov/pubmed/24900987 http://dx.doi.org/10.1155/2014/806391 |
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author | Bruera, Gemma Cannita, Katia Giordano, Aldo Victor Manetta, Rosa Vicentini, Roberto Carducci, Sergio Saltarelli, Patrizia Iapadre, Nerio Coletti, Gino Ficorella, Corrado Ricevuto, Enrico |
author_facet | Bruera, Gemma Cannita, Katia Giordano, Aldo Victor Manetta, Rosa Vicentini, Roberto Carducci, Sergio Saltarelli, Patrizia Iapadre, Nerio Coletti, Gino Ficorella, Corrado Ricevuto, Enrico |
author_sort | Bruera, Gemma |
collection | PubMed |
description | Background. Hepatocellular carcinoma (HCC) patients require different treatment strategies according to disease extension, liver function, and patient's fitness. We evaluated HCC multidisciplinary management in clinical practice. Methods. Consecutive patients were followed and treated with tailored medical, locoregional, and surgical treatments, according to disease stage and patient's fitness (age, Cumulative Illness Rating Scale (CIRS)). Activity, efficacy, and safety were evaluated. Results. Thirty-eight patients were evaluated: median age, 74; elderly 92%; CIRS secondary 28 (74%); Child-Pugh A 20 (53%), B 11 (29%); and Barcelona Clinic Liver Cancer (BCLC) 0 2 (5%), A 9 (24%), B 10 (26%), C 13 (34%), and D 4 (11%). Overall survival (OS) was 30 months. At 9 months median follow-up, among 25 unresectable HCC, OS was 10 months; BCLC B–D unfit for sorafenib showed OS 3 months. Ten patients (40%) received sorafenib: Child-Pugh A 5 (50%) and B 5 (50%) and disease control rate 89%, progression-free survival 7 months, and OS 9 months. G3-4 toxicities: anorexia, hypertransaminaemia, hyperbilirubinemia, and hypercreatininemia. Limiting toxicity syndromes were 40%, all multiple sites. Conclusion. HCC patients require multidisciplinary clinical management to properly select tailored treatments according to disease stage, fitness, and liver function. Patients suitable for sorafenib should be carefully selected, monitored for individual safety, and prevalently characterized by limiting toxicity syndromes multiple sites. |
format | Online Article Text |
id | pubmed-4034404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40344042014-06-04 Multidisciplinary Management of Hepatocellular Carcinoma in Clinical Practice Bruera, Gemma Cannita, Katia Giordano, Aldo Victor Manetta, Rosa Vicentini, Roberto Carducci, Sergio Saltarelli, Patrizia Iapadre, Nerio Coletti, Gino Ficorella, Corrado Ricevuto, Enrico Biomed Res Int Clinical Study Background. Hepatocellular carcinoma (HCC) patients require different treatment strategies according to disease extension, liver function, and patient's fitness. We evaluated HCC multidisciplinary management in clinical practice. Methods. Consecutive patients were followed and treated with tailored medical, locoregional, and surgical treatments, according to disease stage and patient's fitness (age, Cumulative Illness Rating Scale (CIRS)). Activity, efficacy, and safety were evaluated. Results. Thirty-eight patients were evaluated: median age, 74; elderly 92%; CIRS secondary 28 (74%); Child-Pugh A 20 (53%), B 11 (29%); and Barcelona Clinic Liver Cancer (BCLC) 0 2 (5%), A 9 (24%), B 10 (26%), C 13 (34%), and D 4 (11%). Overall survival (OS) was 30 months. At 9 months median follow-up, among 25 unresectable HCC, OS was 10 months; BCLC B–D unfit for sorafenib showed OS 3 months. Ten patients (40%) received sorafenib: Child-Pugh A 5 (50%) and B 5 (50%) and disease control rate 89%, progression-free survival 7 months, and OS 9 months. G3-4 toxicities: anorexia, hypertransaminaemia, hyperbilirubinemia, and hypercreatininemia. Limiting toxicity syndromes were 40%, all multiple sites. Conclusion. HCC patients require multidisciplinary clinical management to properly select tailored treatments according to disease stage, fitness, and liver function. Patients suitable for sorafenib should be carefully selected, monitored for individual safety, and prevalently characterized by limiting toxicity syndromes multiple sites. Hindawi Publishing Corporation 2014 2014-05-08 /pmc/articles/PMC4034404/ /pubmed/24900987 http://dx.doi.org/10.1155/2014/806391 Text en Copyright © 2014 Gemma Bruera et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Bruera, Gemma Cannita, Katia Giordano, Aldo Victor Manetta, Rosa Vicentini, Roberto Carducci, Sergio Saltarelli, Patrizia Iapadre, Nerio Coletti, Gino Ficorella, Corrado Ricevuto, Enrico Multidisciplinary Management of Hepatocellular Carcinoma in Clinical Practice |
title | Multidisciplinary Management of Hepatocellular Carcinoma in Clinical Practice |
title_full | Multidisciplinary Management of Hepatocellular Carcinoma in Clinical Practice |
title_fullStr | Multidisciplinary Management of Hepatocellular Carcinoma in Clinical Practice |
title_full_unstemmed | Multidisciplinary Management of Hepatocellular Carcinoma in Clinical Practice |
title_short | Multidisciplinary Management of Hepatocellular Carcinoma in Clinical Practice |
title_sort | multidisciplinary management of hepatocellular carcinoma in clinical practice |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4034404/ https://www.ncbi.nlm.nih.gov/pubmed/24900987 http://dx.doi.org/10.1155/2014/806391 |
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