Multi-day vs single-day dexamethasone for the prophylaxis of chemotherapy-induced nausea and vomiting: systematic review and meta-analysis.

IF 2.8 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Supportive Care in Cancer Pub Date : 2024-10-21 DOI:10.1007/s00520-024-08934-0
Ronald Chow, Luigi Celio, James Im, Saverio Caini, Lawson Eng, Elizabeth Prsic, Florian Scotté, Matti Aapro
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Abstract

Introduction: Over the past decade, several randomized controlled trials have compared single-day dexamethasone (dexamethasone-sparing) regimens to the current standard multi-day dexamethasone antiemetic regimen for chemotherapy-induced nausea and vomiting (CINV). The aim of this systematic review and meta-analysis is to compare the efficacy and safety of dexamethasone-sparing regimens to standard multi-day dexamethasone, used for the prophylaxis of CINV.

Methods: Ovid Medline and Embase were searched from database inception to March 2024. Studies were included if they reported on randomized controlled trials of adult cancer patients receiving different scheduling of dexamethasone, for the endpoints of complete response, complete control, no nausea, no vomiting, and no use of rescue medication. Safety was also assessed. Meta-analysis, leave-one-out meta-analysis, and cumulative meta-analysis were conducted to generate summary effect estimates and assess the influence of single trials on the summary effect estimate.

Results: Ten trials reporting on 2234 patients were included. Dexamethasone-sparing regimens were found to be no different to control arm in the acute (Risk Ratio [RR] 1.01; 95% CI, 0.94-1.08), delayed (RR 0.97; 95% CI, 0.89-1.05) and overall phases (RR 0.98; 95% CI, 0.90-1.06) for complete response. There was likewise no difference for complete control, no nausea, no vomiting, and no use of rescue medication. Safety profile was similar. There was no concern for bias in the published literature. No difference was found between studies reporting on anthracycline/cyclophosphamide-based highly emetogenic chemotherapy (HEC) and moderately emetogenic chemotherapy (MEC).

Conclusion: In this comprehensive systematic review and meta-analysis, dexamethasone-sparing regimens were found to be no different to current multi-day regimens with respect to efficacy and safety for MEC and anthracycline/cyclophosphamide-based regimens. Clinicians and future guidelines should strongly consider greater adoption and endorsement of dexamethasone-sparing regimens.

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用于预防化疗引起的恶心和呕吐的多日地塞米松与单日地塞米松:系统综述和荟萃分析。
简介:在过去十年中,多项随机对照试验对单日地塞米松(地塞米松保留方案)和目前标准的多日地塞米松止吐方案进行了比较,以治疗化疗引起的恶心和呕吐(CINV)。本系统综述和荟萃分析的目的是比较地塞米松稀释方案与用于预防 CINV 的标准多日地塞米松方案的有效性和安全性:方法:对 Ovid Medline 和 Embase 数据库中从开始到 2024 年 3 月的内容进行检索。如果研究报告了成年癌症患者接受不同剂量地塞米松治疗的随机对照试验,并以完全应答、完全控制、无恶心、无呕吐和未使用抢救药物为终点,则纳入该研究。此外,还对安全性进行了评估。研究人员进行了荟萃分析、剔除荟萃分析和累积荟萃分析,以得出总效应估计值,并评估单项试验对总效应估计值的影响:结果:共纳入了10项试验,报告了2234名患者的情况。在急性期(风险比[RR] 1.01;95% CI,0.94-1.08)、延迟期(RR 0.97;95% CI,0.89-1.05)和总体期(RR 0.98;95% CI,0.90-1.06),地塞米松保留治疗方案与对照组在完全应答方面没有差异。同样,在完全控制、无恶心、无呕吐和不使用抢救药物方面也没有差异。安全性情况相似。已发表的文献中不存在偏倚问题。以蒽环类/环磷酰胺为基础的高致呕吐化疗(HEC)和中度致呕吐化疗(MEC)的研究报告之间未发现差异:在这项全面的系统综述和荟萃分析中发现,在MEC和以蒽环类/环磷酰胺为基础的化疗方案中,地塞米松保留方案在疗效和安全性方面与目前的多日方案没有区别。临床医生和未来的指南应大力考虑更多地采用和认可地塞米松保留方案。
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来源期刊
Supportive Care in Cancer
Supportive Care in Cancer 医学-康复医学
CiteScore
5.70
自引率
9.70%
发文量
751
审稿时长
3 months
期刊介绍: Supportive Care in Cancer provides members of the Multinational Association of Supportive Care in Cancer (MASCC) and all other interested individuals, groups and institutions with the most recent scientific and social information on all aspects of supportive care in cancer patients. It covers primarily medical, technical and surgical topics concerning supportive therapy and care which may supplement or substitute basic cancer treatment at all stages of the disease. Nursing, rehabilitative, psychosocial and spiritual issues of support are also included.
期刊最新文献
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