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Hepatocellular Carcinoma Treatment With Sorafenib: Real-Life Evaluation of Prognostic Factors and a Practical Clue for Patient Management

INTRODUCTION: Sorafenib chemotherapy is the first-line therapy for patients with hepatocellular carcinoma (HCC) in an advanced stage. The aim of this study was to evaluate prognostic factors of survival in HCC patients treated with sorafenib, in real-life clinical practice. MATERIAL AND METHODS: Ret...

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Autores principales: Cardoso, Helder, Alves, Ana Margarida, Marques, Margarida, Vale, Ana Maria, Pereira, Pedro, Macedo, Guilherme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Karger Publishers 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5580019/
https://www.ncbi.nlm.nih.gov/pubmed/28868469
http://dx.doi.org/10.1016/j.jpge.2016.04.006
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author Cardoso, Helder
Alves, Ana Margarida
Marques, Margarida
Vale, Ana Maria
Pereira, Pedro
Macedo, Guilherme
author_facet Cardoso, Helder
Alves, Ana Margarida
Marques, Margarida
Vale, Ana Maria
Pereira, Pedro
Macedo, Guilherme
author_sort Cardoso, Helder
collection PubMed
description INTRODUCTION: Sorafenib chemotherapy is the first-line therapy for patients with hepatocellular carcinoma (HCC) in an advanced stage. The aim of this study was to evaluate prognostic factors of survival in HCC patients treated with sorafenib, in real-life clinical practice. MATERIAL AND METHODS: Retrospective study of HCC patients who initiated treatment with sorafenib, following assessment and indication from the multidisciplinary group. RESULTS: There were included 36 patients, mostly male (89%) and with a mean age of 65 years. The main etiologies were chronic hepatitis C (44%) and alcoholic liver disease (36%). Twenty patients (56%) were classified as Child–Pugh A and 16 patients (44%) as Child–Pugh B. Half of the patients group were staged as BCLC C and the remaining as BCLC B. Significant adverse events were observed in 15 patients (42%) and were associated with longer survival (21.5 vs. 3.2 months, p < 0.001). The most frequent adverse events were diarrhea and palmar-plantar syndrome. Median survival was 17.3 months for Child–Pugh A versus 3.2 months for Child–Pugh B patients (p = 0.001). Within Child–Pugh A, median OS was 21.5 months for BCLC B patients and 15.7 months for BCLC C patients (p = 0.001). DISCUSSION AND CONCLUSIONS: The main prognostic factors beyond Child–Pugh class and BCLC stage included the occurrence of significant adverse events. Being related to increased time of exposure to the drug, it points out the need of dose reducing instead of discontinuation whenever significant adverse events occur.
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spelling pubmed-55800192017-09-01 Hepatocellular Carcinoma Treatment With Sorafenib: Real-Life Evaluation of Prognostic Factors and a Practical Clue for Patient Management Cardoso, Helder Alves, Ana Margarida Marques, Margarida Vale, Ana Maria Pereira, Pedro Macedo, Guilherme GE Port J Gastroenterol Original Article INTRODUCTION: Sorafenib chemotherapy is the first-line therapy for patients with hepatocellular carcinoma (HCC) in an advanced stage. The aim of this study was to evaluate prognostic factors of survival in HCC patients treated with sorafenib, in real-life clinical practice. MATERIAL AND METHODS: Retrospective study of HCC patients who initiated treatment with sorafenib, following assessment and indication from the multidisciplinary group. RESULTS: There were included 36 patients, mostly male (89%) and with a mean age of 65 years. The main etiologies were chronic hepatitis C (44%) and alcoholic liver disease (36%). Twenty patients (56%) were classified as Child–Pugh A and 16 patients (44%) as Child–Pugh B. Half of the patients group were staged as BCLC C and the remaining as BCLC B. Significant adverse events were observed in 15 patients (42%) and were associated with longer survival (21.5 vs. 3.2 months, p < 0.001). The most frequent adverse events were diarrhea and palmar-plantar syndrome. Median survival was 17.3 months for Child–Pugh A versus 3.2 months for Child–Pugh B patients (p = 0.001). Within Child–Pugh A, median OS was 21.5 months for BCLC B patients and 15.7 months for BCLC C patients (p = 0.001). DISCUSSION AND CONCLUSIONS: The main prognostic factors beyond Child–Pugh class and BCLC stage included the occurrence of significant adverse events. Being related to increased time of exposure to the drug, it points out the need of dose reducing instead of discontinuation whenever significant adverse events occur. Karger Publishers 2016-07-06 /pmc/articles/PMC5580019/ /pubmed/28868469 http://dx.doi.org/10.1016/j.jpge.2016.04.006 Text en © 2016 Sociedade Portuguesa de Gastrenterologia. Published by Elsevier Espa˜na, S.L.U. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Cardoso, Helder
Alves, Ana Margarida
Marques, Margarida
Vale, Ana Maria
Pereira, Pedro
Macedo, Guilherme
Hepatocellular Carcinoma Treatment With Sorafenib: Real-Life Evaluation of Prognostic Factors and a Practical Clue for Patient Management
title Hepatocellular Carcinoma Treatment With Sorafenib: Real-Life Evaluation of Prognostic Factors and a Practical Clue for Patient Management
title_full Hepatocellular Carcinoma Treatment With Sorafenib: Real-Life Evaluation of Prognostic Factors and a Practical Clue for Patient Management
title_fullStr Hepatocellular Carcinoma Treatment With Sorafenib: Real-Life Evaluation of Prognostic Factors and a Practical Clue for Patient Management
title_full_unstemmed Hepatocellular Carcinoma Treatment With Sorafenib: Real-Life Evaluation of Prognostic Factors and a Practical Clue for Patient Management
title_short Hepatocellular Carcinoma Treatment With Sorafenib: Real-Life Evaluation of Prognostic Factors and a Practical Clue for Patient Management
title_sort hepatocellular carcinoma treatment with sorafenib: real-life evaluation of prognostic factors and a practical clue for patient management
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5580019/
https://www.ncbi.nlm.nih.gov/pubmed/28868469
http://dx.doi.org/10.1016/j.jpge.2016.04.006
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