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The Safety of Chemotherapy for Breast Cancer Patients with Hepatitis C Virus Infection
Background: Hepatitis C virus (HCV) infection is one of the major causes of chronic liver disease, and more than 880,000 people are estimated to be infected with HCV in Japan. Little information is available on the outcomes of HCV during chemotherapy for solid tumors, and the impact of HCV infection...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3726714/ https://www.ncbi.nlm.nih.gov/pubmed/23901352 http://dx.doi.org/10.7150/jca.6231 |
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author | Miura, Yuji Theriault, Richard L Naito, Yoichi Suyama, Koichi Shimomura, Akihiko Iwatani, Tsuguo Miura, Daishu Kawabata, Hidetaka Kumada, Hiromitsu Takano, Toshimi |
author_facet | Miura, Yuji Theriault, Richard L Naito, Yoichi Suyama, Koichi Shimomura, Akihiko Iwatani, Tsuguo Miura, Daishu Kawabata, Hidetaka Kumada, Hiromitsu Takano, Toshimi |
author_sort | Miura, Yuji |
collection | PubMed |
description | Background: Hepatitis C virus (HCV) infection is one of the major causes of chronic liver disease, and more than 880,000 people are estimated to be infected with HCV in Japan. Little information is available on the outcomes of HCV during chemotherapy for solid tumors, and the impact of HCV infection on toxicity of chemotherapy is unknown. Materials and methods: We performed a retrospective survey of 1,110 patients diagnosed with breast cancer between January 2006 and March 2011 at our institution. All patients had been screened for hepatitis C serology at diagnosis of breast cancer. We retrospectively investigated the change in HCV load and the toxicities of chemotherapy, based on review of their medical records. Results: 23 patients were identified as having a positive test for anti-HCV antibodies. Ten of these patients received chemotherapy. Their median age was 66 years. No patient had decompensated liver disease at baseline. Eight patients received cytotoxic agents with or without trastuzumab, and two patients received trastuzumab alone. Four of eight patients who received cytotoxic chemotherapy developed febrile neutropenia and one developed transaminases elevation. Serum HCV-ribonucleic acid (RNA) level before and after chemotherapy was evaluated in six patients. Median serum HCV-RNA level at baseline and after chemotherapy was 6.5 and 6.7 logIU/ml, respectively. Conclusion: Chemotherapy for breast cancer patients with HCV infection is feasible, and viral load doesn't change during the chemotherapy. |
format | Online Article Text |
id | pubmed-3726714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-37267142013-07-30 The Safety of Chemotherapy for Breast Cancer Patients with Hepatitis C Virus Infection Miura, Yuji Theriault, Richard L Naito, Yoichi Suyama, Koichi Shimomura, Akihiko Iwatani, Tsuguo Miura, Daishu Kawabata, Hidetaka Kumada, Hiromitsu Takano, Toshimi J Cancer Research Paper Background: Hepatitis C virus (HCV) infection is one of the major causes of chronic liver disease, and more than 880,000 people are estimated to be infected with HCV in Japan. Little information is available on the outcomes of HCV during chemotherapy for solid tumors, and the impact of HCV infection on toxicity of chemotherapy is unknown. Materials and methods: We performed a retrospective survey of 1,110 patients diagnosed with breast cancer between January 2006 and March 2011 at our institution. All patients had been screened for hepatitis C serology at diagnosis of breast cancer. We retrospectively investigated the change in HCV load and the toxicities of chemotherapy, based on review of their medical records. Results: 23 patients were identified as having a positive test for anti-HCV antibodies. Ten of these patients received chemotherapy. Their median age was 66 years. No patient had decompensated liver disease at baseline. Eight patients received cytotoxic agents with or without trastuzumab, and two patients received trastuzumab alone. Four of eight patients who received cytotoxic chemotherapy developed febrile neutropenia and one developed transaminases elevation. Serum HCV-ribonucleic acid (RNA) level before and after chemotherapy was evaluated in six patients. Median serum HCV-RNA level at baseline and after chemotherapy was 6.5 and 6.7 logIU/ml, respectively. Conclusion: Chemotherapy for breast cancer patients with HCV infection is feasible, and viral load doesn't change during the chemotherapy. Ivyspring International Publisher 2013-07-24 /pmc/articles/PMC3726714/ /pubmed/23901352 http://dx.doi.org/10.7150/jca.6231 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. |
spellingShingle | Research Paper Miura, Yuji Theriault, Richard L Naito, Yoichi Suyama, Koichi Shimomura, Akihiko Iwatani, Tsuguo Miura, Daishu Kawabata, Hidetaka Kumada, Hiromitsu Takano, Toshimi The Safety of Chemotherapy for Breast Cancer Patients with Hepatitis C Virus Infection |
title | The Safety of Chemotherapy for Breast Cancer Patients with Hepatitis C Virus Infection |
title_full | The Safety of Chemotherapy for Breast Cancer Patients with Hepatitis C Virus Infection |
title_fullStr | The Safety of Chemotherapy for Breast Cancer Patients with Hepatitis C Virus Infection |
title_full_unstemmed | The Safety of Chemotherapy for Breast Cancer Patients with Hepatitis C Virus Infection |
title_short | The Safety of Chemotherapy for Breast Cancer Patients with Hepatitis C Virus Infection |
title_sort | safety of chemotherapy for breast cancer patients with hepatitis c virus infection |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3726714/ https://www.ncbi.nlm.nih.gov/pubmed/23901352 http://dx.doi.org/10.7150/jca.6231 |
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