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Efficacy of Goshajinkigan for Peripheral Neurotoxicity of Oxaliplatin in Patients with Advanced or Recurrent Colorectal Cancer
Peripheral neurotoxicity is the major limiting factor for oxaliplatin therapy. Goshajinkigan (GJG), a traditional Japanese herbal medicine, was recently shown to be effective in protecting against the neurotoxicity of taxanes in Japan. We retrospectively investigated the effect of GJG on peripheral...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135601/ https://www.ncbi.nlm.nih.gov/pubmed/19952054 http://dx.doi.org/10.1093/ecam/nep200 |
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author | Kono, Toru Mamiya, Noriaki Chisato, Naoyuki Ebisawa, Yosiaki Yamazaki, Hirotaka Watari, Jiro Yamamoto, Yasuhiro Suzuki, Shigetaka Asama, Toshiyuki Kamiya, Kazunori |
author_facet | Kono, Toru Mamiya, Noriaki Chisato, Naoyuki Ebisawa, Yosiaki Yamazaki, Hirotaka Watari, Jiro Yamamoto, Yasuhiro Suzuki, Shigetaka Asama, Toshiyuki Kamiya, Kazunori |
author_sort | Kono, Toru |
collection | PubMed |
description | Peripheral neurotoxicity is the major limiting factor for oxaliplatin therapy. Goshajinkigan (GJG), a traditional Japanese herbal medicine, was recently shown to be effective in protecting against the neurotoxicity of taxanes in Japan. We retrospectively investigated the effect of GJG on peripheral neurotoxicity associated with oxaliplatin therapy. Ninety patients with metastatic colorectal cancer that received FOLFOX4 or modified FOLFOX6 therapy were assigned to receive one of the following adjuncts: oral GJG at 7.5 g day(−1) (Group A, n = 11), intravenous supplementation of calcium gluconate and magnesium sulfate (1 g each before and after FOLFOX) (Group B, n = 14), combined GJG and calcium gluconate and magnesium sulfate therapies (Group C, n = 21), or no concomitant therapy (Group D, n = 44). The incidence of peripheral neurotoxicity was investigated when the cumulative dose of oxaliplatin exceeded 500 mg m(−2). When the cumulative dose of oxaliplatin exceeded 500 mg m(−2), the incidence of neuropathy (all grades) in Groups A–D was 50.0%, 100%, 78.9%, and 91.7%, respectively. It was lowest in the group that received GJG alone. Concomitant administration of GJG reduced the neurotoxicity of oxaliplatin in patients that received chemotherapy for colorectal cancer. |
format | Online Article Text |
id | pubmed-3135601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-31356012011-07-22 Efficacy of Goshajinkigan for Peripheral Neurotoxicity of Oxaliplatin in Patients with Advanced or Recurrent Colorectal Cancer Kono, Toru Mamiya, Noriaki Chisato, Naoyuki Ebisawa, Yosiaki Yamazaki, Hirotaka Watari, Jiro Yamamoto, Yasuhiro Suzuki, Shigetaka Asama, Toshiyuki Kamiya, Kazunori Evid Based Complement Alternat Med Original Article Peripheral neurotoxicity is the major limiting factor for oxaliplatin therapy. Goshajinkigan (GJG), a traditional Japanese herbal medicine, was recently shown to be effective in protecting against the neurotoxicity of taxanes in Japan. We retrospectively investigated the effect of GJG on peripheral neurotoxicity associated with oxaliplatin therapy. Ninety patients with metastatic colorectal cancer that received FOLFOX4 or modified FOLFOX6 therapy were assigned to receive one of the following adjuncts: oral GJG at 7.5 g day(−1) (Group A, n = 11), intravenous supplementation of calcium gluconate and magnesium sulfate (1 g each before and after FOLFOX) (Group B, n = 14), combined GJG and calcium gluconate and magnesium sulfate therapies (Group C, n = 21), or no concomitant therapy (Group D, n = 44). The incidence of peripheral neurotoxicity was investigated when the cumulative dose of oxaliplatin exceeded 500 mg m(−2). When the cumulative dose of oxaliplatin exceeded 500 mg m(−2), the incidence of neuropathy (all grades) in Groups A–D was 50.0%, 100%, 78.9%, and 91.7%, respectively. It was lowest in the group that received GJG alone. Concomitant administration of GJG reduced the neurotoxicity of oxaliplatin in patients that received chemotherapy for colorectal cancer. Hindawi Publishing Corporation 2011 2011-01-11 /pmc/articles/PMC3135601/ /pubmed/19952054 http://dx.doi.org/10.1093/ecam/nep200 Text en Copyright © 2011 Toru Kono 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 | Original Article Kono, Toru Mamiya, Noriaki Chisato, Naoyuki Ebisawa, Yosiaki Yamazaki, Hirotaka Watari, Jiro Yamamoto, Yasuhiro Suzuki, Shigetaka Asama, Toshiyuki Kamiya, Kazunori Efficacy of Goshajinkigan for Peripheral Neurotoxicity of Oxaliplatin in Patients with Advanced or Recurrent Colorectal Cancer |
title | Efficacy of Goshajinkigan for Peripheral Neurotoxicity of Oxaliplatin in Patients with Advanced or Recurrent Colorectal Cancer |
title_full | Efficacy of Goshajinkigan for Peripheral Neurotoxicity of Oxaliplatin in Patients with Advanced or Recurrent Colorectal Cancer |
title_fullStr | Efficacy of Goshajinkigan for Peripheral Neurotoxicity of Oxaliplatin in Patients with Advanced or Recurrent Colorectal Cancer |
title_full_unstemmed | Efficacy of Goshajinkigan for Peripheral Neurotoxicity of Oxaliplatin in Patients with Advanced or Recurrent Colorectal Cancer |
title_short | Efficacy of Goshajinkigan for Peripheral Neurotoxicity of Oxaliplatin in Patients with Advanced or Recurrent Colorectal Cancer |
title_sort | efficacy of goshajinkigan for peripheral neurotoxicity of oxaliplatin in patients with advanced or recurrent colorectal cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135601/ https://www.ncbi.nlm.nih.gov/pubmed/19952054 http://dx.doi.org/10.1093/ecam/nep200 |
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