Efficacy and safety of dexamethasone sparing for the prevention of nausea and vomiting associated with moderately emetogenic chemotherapy: a systematic review and meta-analysis of Clinical Practice Guidelines for Antiemesis 2023 from Japan Society of Clinical Oncology.

IF 2.4 3区 医学 Q3 ONCOLOGY International Journal of Clinical Oncology Pub Date : 2024-12-01 Epub Date: 2024-10-17 DOI:10.1007/s10147-024-02643-8
Kazuhisa Nakashima, Ayako Yokomizo, Michiyasu Murakami, Kenji Okita, Makoto Wada, Keiko Iino, Tatsuo Akechi, Hirotoshi Iihara, Chiyo K Imamura, Ayako Okuyama, Keiko Ozawa, Yong-Il Kim, Hidenori Sasaki, Eriko Satomi, Masayuki Takeda, Ryuhei Tanaka, Takako Eguchi Nakajima, Naoki Nakamura, Junichi Nishimura, Mayumi Noda, Kazumi Hayashi, Takahiro Higashi, Narikazu Boku, Koji Matsumoto, Yoko Matsumoto, Nobuyuki Yamamoto, Kenjiro Aogi, Masakazu Abe
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Abstract

Background: Palonosetron, a second-generation 5-HT3 receptor antagonist (5-HT3RA), is more effective than first-generation 5-HT3RA. Several studies have investigated whether dexamethasone (DEX), when combined with palonosetron as a 5-HT3RA, can be spared in the delayed phase after moderately emetogenic chemotherapy (MEC). In this systematic review, we aimed to determine which between 1- and 3-day DEX administration, when combined with palonosetron, is more useful in patients receiving MEC.

Methods: The PubMed, Cochrane Library, and Ichushi-Web databases were searched for relevant studies published between 1990 and 2020. We included studies that compared the efficacy of 1- and 3-day DEX administration in preventing nausea and vomiting associated with MEC. Outcomes were "prevention of vomiting (complete response rate and no vomiting rate)," "prevention of nausea" (complete control rate, total control rate, no nausea rate, and no clinically significant nausea rate)" in the delayed phase, "prevention of blood glucose level elevation," and "prevention of osteoporosis."

Results: Eight studies were included in this systematic review. The no vomiting rate was significantly higher in the 3-day DEX group than in the 1-day DEX group. However, the other efficacy items did not significantly differ between the two groups. Meanwhile, insufficient evidence was obtained for "prevention of blood glucose level elevation" and "prevention of osteoporosis."

Conclusions: No significant differences in most antiemetic effects were found between 1- and 3-day DEX administration. Thus, DEX administration could be shortened from 3 days to 1 day when used in combination with palonosetron.

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地塞米松疏松预防中度致吐化疗相关恶心和呕吐的疗效和安全性:日本临床肿瘤学会《止吐临床实践指南 2023》的系统回顾和荟萃分析。
背景:第二代5-HT3受体拮抗剂(5-HT3RA)帕洛诺司琼比第一代5-HT3RA更有效。有几项研究探讨了地塞米松(DEX)与帕洛诺司琼(5-HT3RA)联合使用时,是否可以在中度致吐化疗(MEC)后的延迟期避免使用地塞米松。在本系统综述中,我们旨在确定 1 天和 3 天的 DEX 给药与帕洛诺司琼联用时,哪一种对接受中度致吐化疗的患者更有用:我们在 PubMed、Cochrane Library 和 Ichushi-Web 数据库中检索了 1990 年至 2020 年间发表的相关研究。我们纳入了比较 1 天和 3 天服用 DEX 对预防与 MEC 相关的恶心和呕吐疗效的研究。研究结果包括延迟阶段的 "预防呕吐(完全反应率和无呕吐率)"、"预防恶心"(完全控制率、完全控制率、无恶心率和无临床显著恶心率)、"预防血糖水平升高 "和 "预防骨质疏松":本系统综述共纳入 8 项研究。3天DEX组的无呕吐率明显高于1天DEX组。然而,两组之间的其他疗效项目并无明显差异。同时,"预防血糖升高 "和 "预防骨质疏松 "的证据不足:服用1天和3天DEX的大多数止吐效果无明显差异。因此,DEX与帕洛诺司琼合用时,用药时间可从3天缩短至1天。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.80
自引率
3.00%
发文量
175
审稿时长
2 months
期刊介绍: The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.
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