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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
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.
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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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