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Changes in plasma vascular endothelial growth factor at 8 weeks after sorafenib administration as predictors of survival for advanced hepatocellular carcinoma
BACKGROUND: A new predictive biomarker for determining prognosis in patients with hepatocellular carcinoma (HCC) who receive sorafenib is required, because achieving a reduction in tumor size with sorafenib is rare, even in patients who have a favorable prognosis. Vascular endothelial growth factor...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4209122/ https://www.ncbi.nlm.nih.gov/pubmed/24122122 http://dx.doi.org/10.1002/cncr.28384 |
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author | Tsuchiya, Kaoru Asahina, Yasuhiro Matsuda, Shuya Muraoka, Masaru Nakata, Toru Suzuki, Yuichiro Tamaki, Nobuharu Yasui, Yutaka Suzuki, Shoko Hosokawa, Takanori Nishimura, Takashi Ueda, Ken Kuzuya, Teiji Nakanishi, Hiroyuki Itakura, Jun Takahashi, Yuka Kurosaki, Masayuki Enomoto, Nobuyuki Izumi, Namiki |
author_facet | Tsuchiya, Kaoru Asahina, Yasuhiro Matsuda, Shuya Muraoka, Masaru Nakata, Toru Suzuki, Yuichiro Tamaki, Nobuharu Yasui, Yutaka Suzuki, Shoko Hosokawa, Takanori Nishimura, Takashi Ueda, Ken Kuzuya, Teiji Nakanishi, Hiroyuki Itakura, Jun Takahashi, Yuka Kurosaki, Masayuki Enomoto, Nobuyuki Izumi, Namiki |
author_sort | Tsuchiya, Kaoru |
collection | PubMed |
description | BACKGROUND: A new predictive biomarker for determining prognosis in patients with hepatocellular carcinoma (HCC) who receive sorafenib is required, because achieving a reduction in tumor size with sorafenib is rare, even in patients who have a favorable prognosis. Vascular endothelial growth factor (VEGF) receptor is a sorafenib target. In the current study, the authors examined changes in plasma VEGF concentrations during sorafenib treatment and determined the clinical significance of VEGF as a prognostic indicator in patients with HCC. METHODS: Plasma VEGF concentrations were serially measured in 63 patients with advanced HCC before and during sorafenib treatment. A plasma VEGF concentration that decreased >5% from the pretreatment level at 8 weeks was defined as a “VEGF decrease.” An objective tumor response was determined using modified Response Evaluation Criteria in Solid Tumors 1 month after the initiation of therapy and every 3 months thereafter. RESULTS: Patients who had a VEGF decrease at week 8 (n = 14) had a longer median survival than those who did not have a VEGF decrease (n = 49; 30.9 months vs 14.4 months; P = .038). All patients who had a VEGF decrease survived for >6 months, and the patients who had both a VEGF decrease and an α-fetoprotein response (n = 6) survived during the observation period (median, 19.7 months; range, 6.5-31.0 months). In univariate analyses, a VEGF decrease, radiologic findings classified as progressive disease, and major vascular invasion were associated significantly with 1-year survival; and, in multivariate analysis, a VEGF decrease was identified as an independent factor associated significantly with survival. CONCLUSIONS: A plasma VEGF concentration decrease at 8 weeks after starting sorafenib treatment may predict favorable overall survival in patients with advanced HCC. |
format | Online Article Text |
id | pubmed-4209122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42091222014-11-14 Changes in plasma vascular endothelial growth factor at 8 weeks after sorafenib administration as predictors of survival for advanced hepatocellular carcinoma Tsuchiya, Kaoru Asahina, Yasuhiro Matsuda, Shuya Muraoka, Masaru Nakata, Toru Suzuki, Yuichiro Tamaki, Nobuharu Yasui, Yutaka Suzuki, Shoko Hosokawa, Takanori Nishimura, Takashi Ueda, Ken Kuzuya, Teiji Nakanishi, Hiroyuki Itakura, Jun Takahashi, Yuka Kurosaki, Masayuki Enomoto, Nobuyuki Izumi, Namiki Cancer Original Articles BACKGROUND: A new predictive biomarker for determining prognosis in patients with hepatocellular carcinoma (HCC) who receive sorafenib is required, because achieving a reduction in tumor size with sorafenib is rare, even in patients who have a favorable prognosis. Vascular endothelial growth factor (VEGF) receptor is a sorafenib target. In the current study, the authors examined changes in plasma VEGF concentrations during sorafenib treatment and determined the clinical significance of VEGF as a prognostic indicator in patients with HCC. METHODS: Plasma VEGF concentrations were serially measured in 63 patients with advanced HCC before and during sorafenib treatment. A plasma VEGF concentration that decreased >5% from the pretreatment level at 8 weeks was defined as a “VEGF decrease.” An objective tumor response was determined using modified Response Evaluation Criteria in Solid Tumors 1 month after the initiation of therapy and every 3 months thereafter. RESULTS: Patients who had a VEGF decrease at week 8 (n = 14) had a longer median survival than those who did not have a VEGF decrease (n = 49; 30.9 months vs 14.4 months; P = .038). All patients who had a VEGF decrease survived for >6 months, and the patients who had both a VEGF decrease and an α-fetoprotein response (n = 6) survived during the observation period (median, 19.7 months; range, 6.5-31.0 months). In univariate analyses, a VEGF decrease, radiologic findings classified as progressive disease, and major vascular invasion were associated significantly with 1-year survival; and, in multivariate analysis, a VEGF decrease was identified as an independent factor associated significantly with survival. CONCLUSIONS: A plasma VEGF concentration decrease at 8 weeks after starting sorafenib treatment may predict favorable overall survival in patients with advanced HCC. BlackWell Publishing Ltd 2014-01-15 2013-10-07 /pmc/articles/PMC4209122/ /pubmed/24122122 http://dx.doi.org/10.1002/cncr.28384 Text en © 2013 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Tsuchiya, Kaoru Asahina, Yasuhiro Matsuda, Shuya Muraoka, Masaru Nakata, Toru Suzuki, Yuichiro Tamaki, Nobuharu Yasui, Yutaka Suzuki, Shoko Hosokawa, Takanori Nishimura, Takashi Ueda, Ken Kuzuya, Teiji Nakanishi, Hiroyuki Itakura, Jun Takahashi, Yuka Kurosaki, Masayuki Enomoto, Nobuyuki Izumi, Namiki Changes in plasma vascular endothelial growth factor at 8 weeks after sorafenib administration as predictors of survival for advanced hepatocellular carcinoma |
title | Changes in plasma vascular endothelial growth factor at 8 weeks after sorafenib administration as predictors of survival for advanced hepatocellular carcinoma |
title_full | Changes in plasma vascular endothelial growth factor at 8 weeks after sorafenib administration as predictors of survival for advanced hepatocellular carcinoma |
title_fullStr | Changes in plasma vascular endothelial growth factor at 8 weeks after sorafenib administration as predictors of survival for advanced hepatocellular carcinoma |
title_full_unstemmed | Changes in plasma vascular endothelial growth factor at 8 weeks after sorafenib administration as predictors of survival for advanced hepatocellular carcinoma |
title_short | Changes in plasma vascular endothelial growth factor at 8 weeks after sorafenib administration as predictors of survival for advanced hepatocellular carcinoma |
title_sort | changes in plasma vascular endothelial growth factor at 8 weeks after sorafenib administration as predictors of survival for advanced hepatocellular carcinoma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4209122/ https://www.ncbi.nlm.nih.gov/pubmed/24122122 http://dx.doi.org/10.1002/cncr.28384 |
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