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Effects of adding a neurokinin-1 receptor antagonist to 5 mg olanzapine, a 5-hydroxytryptamine-3 receptor antagonist, and dexamethasone for preventing carboplatin-induced nausea and vomiting: a propensity score-matched analysis
BACKGROUND: Olanzapine has been reported to be an effective antiemetic in patients receiving carboplatin-based chemotherapy. However, the efficacy of a neurokinin-1 receptor antagonist (NK(1)RA) added to olanzapine, a 5-hydroxytryptamine-3 receptor antagonist (5-HT(3)RA), and dexamethasone (DEX) has...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941806/ https://www.ncbi.nlm.nih.gov/pubmed/35321690 http://dx.doi.org/10.1186/s12885-022-09392-9 |
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author | Yamamoto, Senri Iihara, Hirotoshi Uozumi, Ryuji Kawazoe, Hitoshi Tanaka, Kazuki Fujita, Yukiyoshi Abe, Masakazu Imai, Hisao Karayama, Masato Hayasaki, Yoh Hirose, Chiemi Suda, Takafumi Nakamura, Kazuto Suzuki, Akio Ohno, Yasushi Morishige, Ken-ichirou Inui, Naoki |
author_facet | Yamamoto, Senri Iihara, Hirotoshi Uozumi, Ryuji Kawazoe, Hitoshi Tanaka, Kazuki Fujita, Yukiyoshi Abe, Masakazu Imai, Hisao Karayama, Masato Hayasaki, Yoh Hirose, Chiemi Suda, Takafumi Nakamura, Kazuto Suzuki, Akio Ohno, Yasushi Morishige, Ken-ichirou Inui, Naoki |
author_sort | Yamamoto, Senri |
collection | PubMed |
description | BACKGROUND: Olanzapine has been reported to be an effective antiemetic in patients receiving carboplatin-based chemotherapy. However, the efficacy of a neurokinin-1 receptor antagonist (NK(1)RA) added to olanzapine, a 5-hydroxytryptamine-3 receptor antagonist (5-HT(3)RA), and dexamethasone (DEX) has not been proven. This study aimed to assess the efficacy and safety of NK(1)RA, in combination with three-drug antiemetic regimens containing olanzapine, in preventing nausea and vomiting induced by carboplatin-based chemotherapy. METHODS: Data were pooled for 140 patients receiving carboplatin-based chemotherapy from three multicenter, prospective, single-arm, open-label phase II studies that evaluated the efficacy and safety of olanzapine for chemotherapy-induced nausea and vomiting. The propensity score of the co-administration of NK(1)RA was estimated for each patient using a logistic regression model that included age, sex, and carboplatin dose. We analyzed a total of 62 patients, who were treated without NK(1)RA (non-NK(1)RA group: 31 patients) and with NK(1)RA (NK(1)RA group: 31 patients). The patients were selected using propensity score matching. RESULTS: The complete response rate (without emetic episodes or with no administration of rescue medication) in the overall period (0–120 h post carboplatin administration) was 93.5% in the non-NK(1)RA group and 96.8% in the NK(1)RA group, with a difference of -3.2% (95% confidence interval, -18.7% to 10.9%; P = 1.000). In terms of safety, there was no significant difference between the groups in daytime sleepiness and concentration impairment, which are the most worrisome adverse events induced by olanzapine. CONCLUSIONS: The findings suggest that antiemetic regimens consisting of olanzapine, 5HT(3)RA, and DEX without NK(1)RA may be a treatment option for patients receiving carboplatin-based chemotherapy. |
format | Online Article Text |
id | pubmed-8941806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89418062022-03-24 Effects of adding a neurokinin-1 receptor antagonist to 5 mg olanzapine, a 5-hydroxytryptamine-3 receptor antagonist, and dexamethasone for preventing carboplatin-induced nausea and vomiting: a propensity score-matched analysis Yamamoto, Senri Iihara, Hirotoshi Uozumi, Ryuji Kawazoe, Hitoshi Tanaka, Kazuki Fujita, Yukiyoshi Abe, Masakazu Imai, Hisao Karayama, Masato Hayasaki, Yoh Hirose, Chiemi Suda, Takafumi Nakamura, Kazuto Suzuki, Akio Ohno, Yasushi Morishige, Ken-ichirou Inui, Naoki BMC Cancer Research BACKGROUND: Olanzapine has been reported to be an effective antiemetic in patients receiving carboplatin-based chemotherapy. However, the efficacy of a neurokinin-1 receptor antagonist (NK(1)RA) added to olanzapine, a 5-hydroxytryptamine-3 receptor antagonist (5-HT(3)RA), and dexamethasone (DEX) has not been proven. This study aimed to assess the efficacy and safety of NK(1)RA, in combination with three-drug antiemetic regimens containing olanzapine, in preventing nausea and vomiting induced by carboplatin-based chemotherapy. METHODS: Data were pooled for 140 patients receiving carboplatin-based chemotherapy from three multicenter, prospective, single-arm, open-label phase II studies that evaluated the efficacy and safety of olanzapine for chemotherapy-induced nausea and vomiting. The propensity score of the co-administration of NK(1)RA was estimated for each patient using a logistic regression model that included age, sex, and carboplatin dose. We analyzed a total of 62 patients, who were treated without NK(1)RA (non-NK(1)RA group: 31 patients) and with NK(1)RA (NK(1)RA group: 31 patients). The patients were selected using propensity score matching. RESULTS: The complete response rate (without emetic episodes or with no administration of rescue medication) in the overall period (0–120 h post carboplatin administration) was 93.5% in the non-NK(1)RA group and 96.8% in the NK(1)RA group, with a difference of -3.2% (95% confidence interval, -18.7% to 10.9%; P = 1.000). In terms of safety, there was no significant difference between the groups in daytime sleepiness and concentration impairment, which are the most worrisome adverse events induced by olanzapine. CONCLUSIONS: The findings suggest that antiemetic regimens consisting of olanzapine, 5HT(3)RA, and DEX without NK(1)RA may be a treatment option for patients receiving carboplatin-based chemotherapy. BioMed Central 2022-03-23 /pmc/articles/PMC8941806/ /pubmed/35321690 http://dx.doi.org/10.1186/s12885-022-09392-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yamamoto, Senri Iihara, Hirotoshi Uozumi, Ryuji Kawazoe, Hitoshi Tanaka, Kazuki Fujita, Yukiyoshi Abe, Masakazu Imai, Hisao Karayama, Masato Hayasaki, Yoh Hirose, Chiemi Suda, Takafumi Nakamura, Kazuto Suzuki, Akio Ohno, Yasushi Morishige, Ken-ichirou Inui, Naoki Effects of adding a neurokinin-1 receptor antagonist to 5 mg olanzapine, a 5-hydroxytryptamine-3 receptor antagonist, and dexamethasone for preventing carboplatin-induced nausea and vomiting: a propensity score-matched analysis |
title | Effects of adding a neurokinin-1 receptor antagonist to 5 mg olanzapine, a 5-hydroxytryptamine-3 receptor antagonist, and dexamethasone for preventing carboplatin-induced nausea and vomiting: a propensity score-matched analysis |
title_full | Effects of adding a neurokinin-1 receptor antagonist to 5 mg olanzapine, a 5-hydroxytryptamine-3 receptor antagonist, and dexamethasone for preventing carboplatin-induced nausea and vomiting: a propensity score-matched analysis |
title_fullStr | Effects of adding a neurokinin-1 receptor antagonist to 5 mg olanzapine, a 5-hydroxytryptamine-3 receptor antagonist, and dexamethasone for preventing carboplatin-induced nausea and vomiting: a propensity score-matched analysis |
title_full_unstemmed | Effects of adding a neurokinin-1 receptor antagonist to 5 mg olanzapine, a 5-hydroxytryptamine-3 receptor antagonist, and dexamethasone for preventing carboplatin-induced nausea and vomiting: a propensity score-matched analysis |
title_short | Effects of adding a neurokinin-1 receptor antagonist to 5 mg olanzapine, a 5-hydroxytryptamine-3 receptor antagonist, and dexamethasone for preventing carboplatin-induced nausea and vomiting: a propensity score-matched analysis |
title_sort | effects of adding a neurokinin-1 receptor antagonist to 5 mg olanzapine, a 5-hydroxytryptamine-3 receptor antagonist, and dexamethasone for preventing carboplatin-induced nausea and vomiting: a propensity score-matched analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941806/ https://www.ncbi.nlm.nih.gov/pubmed/35321690 http://dx.doi.org/10.1186/s12885-022-09392-9 |
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