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Rikkunshito for Preventing Chemotherapy-Induced Nausea and Vomiting in Lung Cancer Patients: Results from 2 Prospective, Randomized Phase 2 Trials
The herbal medicine rikkunshito has the potential to improve chemotherapy-induced nausea and vomiting (CINV) by stimulating ghrelin secretion. We aimed to evaluate the efficacy and safety of rikkunshito in preventing CINV for patients with lung cancer. Two separate prospective, randomized, phase II...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776023/ https://www.ncbi.nlm.nih.gov/pubmed/29387008 http://dx.doi.org/10.3389/fphar.2017.00972 |
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author | Harada, Toshiyuki Amano, Toraji Ikari, Tomoo Takamura, Kei Ogi, Takahiro Fujikane, Toshiaki Fujita, Yuka Taima, Kageaki Tanaka, Hisashi Sasaki, Takaaki Okumura, Shunsuke Sugawara, Shunichi Yokouchi, Hiroshi Yamada, Noriyuki Morikawa, Naoto Dosaka-Akita, Hirotoshi Isobe, Hiroshi Nishimura, Masaharu |
author_facet | Harada, Toshiyuki Amano, Toraji Ikari, Tomoo Takamura, Kei Ogi, Takahiro Fujikane, Toshiaki Fujita, Yuka Taima, Kageaki Tanaka, Hisashi Sasaki, Takaaki Okumura, Shunsuke Sugawara, Shunichi Yokouchi, Hiroshi Yamada, Noriyuki Morikawa, Naoto Dosaka-Akita, Hirotoshi Isobe, Hiroshi Nishimura, Masaharu |
author_sort | Harada, Toshiyuki |
collection | PubMed |
description | The herbal medicine rikkunshito has the potential to improve chemotherapy-induced nausea and vomiting (CINV) by stimulating ghrelin secretion. We aimed to evaluate the efficacy and safety of rikkunshito in preventing CINV for patients with lung cancer. Two separate prospective, randomized, phase II parallel design studies were conducted in patients with lung cancer. Fifty-eight and sixty-two patients scheduled to receive highly emetogenic chemotherapy (HEC) and moderately emetogenic chemotherapy (MEC), respectively, were randomized 1:1 to receive either standard antiemetic therapy in accordance with international guidelines (S group) or standard antiemetic therapy plus oral rikkunshito (R group). The primary endpoint was overall complete response (CR)—that is, no emesis and rescue medication in the first 120 h post-chemotherapy. Secondary endpoints included CR in the acute (0–24 h) and delayed (>24–120 h) phases and safety. Fifty-seven patients (S group, 28; R group, 29) receiving HEC and sixty-two patients (S group, 30; R group, 32) receiving MEC with comparable characteristics were evaluated. The CR rates were similar across the S and R groups for the HEC study in the overall (67.9% vs. 62.1%), acute (96.4% vs. 89.6%), and delayed (67.9% vs. 62.1%) phases, respectively, and for the MEC study in the overall (83.3% vs. 84.4%), acute (100% vs. 100%), and delayed (83.3% vs. 84.4%) phases, respectively. No severe adverse events were observed. Although rikkunshito was well tolerated, it did not demonstrate an additional preventative effect against CINV in lung cancer patients receiving HEC or MEC. Clinical Trial Registry Information: This study is registered with the University Hospital Medical Information Network (UMIN) Clinical Trial Registry(), identification numbers UMIN 000014239 and UMIN 000014240. |
format | Online Article Text |
id | pubmed-5776023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57760232018-01-31 Rikkunshito for Preventing Chemotherapy-Induced Nausea and Vomiting in Lung Cancer Patients: Results from 2 Prospective, Randomized Phase 2 Trials Harada, Toshiyuki Amano, Toraji Ikari, Tomoo Takamura, Kei Ogi, Takahiro Fujikane, Toshiaki Fujita, Yuka Taima, Kageaki Tanaka, Hisashi Sasaki, Takaaki Okumura, Shunsuke Sugawara, Shunichi Yokouchi, Hiroshi Yamada, Noriyuki Morikawa, Naoto Dosaka-Akita, Hirotoshi Isobe, Hiroshi Nishimura, Masaharu Front Pharmacol Pharmacology The herbal medicine rikkunshito has the potential to improve chemotherapy-induced nausea and vomiting (CINV) by stimulating ghrelin secretion. We aimed to evaluate the efficacy and safety of rikkunshito in preventing CINV for patients with lung cancer. Two separate prospective, randomized, phase II parallel design studies were conducted in patients with lung cancer. Fifty-eight and sixty-two patients scheduled to receive highly emetogenic chemotherapy (HEC) and moderately emetogenic chemotherapy (MEC), respectively, were randomized 1:1 to receive either standard antiemetic therapy in accordance with international guidelines (S group) or standard antiemetic therapy plus oral rikkunshito (R group). The primary endpoint was overall complete response (CR)—that is, no emesis and rescue medication in the first 120 h post-chemotherapy. Secondary endpoints included CR in the acute (0–24 h) and delayed (>24–120 h) phases and safety. Fifty-seven patients (S group, 28; R group, 29) receiving HEC and sixty-two patients (S group, 30; R group, 32) receiving MEC with comparable characteristics were evaluated. The CR rates were similar across the S and R groups for the HEC study in the overall (67.9% vs. 62.1%), acute (96.4% vs. 89.6%), and delayed (67.9% vs. 62.1%) phases, respectively, and for the MEC study in the overall (83.3% vs. 84.4%), acute (100% vs. 100%), and delayed (83.3% vs. 84.4%) phases, respectively. No severe adverse events were observed. Although rikkunshito was well tolerated, it did not demonstrate an additional preventative effect against CINV in lung cancer patients receiving HEC or MEC. Clinical Trial Registry Information: This study is registered with the University Hospital Medical Information Network (UMIN) Clinical Trial Registry(), identification numbers UMIN 000014239 and UMIN 000014240. Frontiers Media S.A. 2018-01-16 /pmc/articles/PMC5776023/ /pubmed/29387008 http://dx.doi.org/10.3389/fphar.2017.00972 Text en Copyright © 2018 Harada, Amano, Ikari, Takamura, Ogi, Fujikane, Fujita, Taima, Tanaka, Sasaki, Okumura, Sugawara, Yokouchi, Yamada, Morikawa, Dosaka-Akita, Isobe and Nishimura. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Harada, Toshiyuki Amano, Toraji Ikari, Tomoo Takamura, Kei Ogi, Takahiro Fujikane, Toshiaki Fujita, Yuka Taima, Kageaki Tanaka, Hisashi Sasaki, Takaaki Okumura, Shunsuke Sugawara, Shunichi Yokouchi, Hiroshi Yamada, Noriyuki Morikawa, Naoto Dosaka-Akita, Hirotoshi Isobe, Hiroshi Nishimura, Masaharu Rikkunshito for Preventing Chemotherapy-Induced Nausea and Vomiting in Lung Cancer Patients: Results from 2 Prospective, Randomized Phase 2 Trials |
title | Rikkunshito for Preventing Chemotherapy-Induced Nausea and Vomiting in Lung Cancer Patients: Results from 2 Prospective, Randomized Phase 2 Trials |
title_full | Rikkunshito for Preventing Chemotherapy-Induced Nausea and Vomiting in Lung Cancer Patients: Results from 2 Prospective, Randomized Phase 2 Trials |
title_fullStr | Rikkunshito for Preventing Chemotherapy-Induced Nausea and Vomiting in Lung Cancer Patients: Results from 2 Prospective, Randomized Phase 2 Trials |
title_full_unstemmed | Rikkunshito for Preventing Chemotherapy-Induced Nausea and Vomiting in Lung Cancer Patients: Results from 2 Prospective, Randomized Phase 2 Trials |
title_short | Rikkunshito for Preventing Chemotherapy-Induced Nausea and Vomiting in Lung Cancer Patients: Results from 2 Prospective, Randomized Phase 2 Trials |
title_sort | rikkunshito for preventing chemotherapy-induced nausea and vomiting in lung cancer patients: results from 2 prospective, randomized phase 2 trials |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776023/ https://www.ncbi.nlm.nih.gov/pubmed/29387008 http://dx.doi.org/10.3389/fphar.2017.00972 |
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