Evaluating the efficacy of a premedication regimen including high-dose cetirizine in reduction of hypersensitivity reactions to paclitaxel: A retrospective cohort study.

IF 1 4区 医学 Q4 ONCOLOGY
Journal of Oncology Pharmacy Practice Pub Date : 2025-07-01 Epub Date: 2024-07-23 DOI:10.1177/10781552241263832
Alexander Hutchinson, Kelly Weaver, Bakeerathan Gunaratnam, Lesley Volz, Lauren Ingles, Lindsay Figg
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Abstract

IntroductionHypersensitivity reactions (HSR) are a known adverse effect of paclitaxel, occurring in approximately 10% of patients, typically during the first or second infusion of the medication. Corticosteroids, histamine-1 and histamine-2 receptor antagonists are given prior to paclitaxel infusions to reduce the incidence of HSR. There are limited data that suggest administration of cetirizine given prior to a platinum infusion as secondary prophylaxis may reduce HSR rates.MethodsThe objective of this study was to assess the impact of a novel paclitaxel hypersensitivity prevention protocol including high-dose cetirizine administered 12 and 6 h prior to paclitaxel infusion on the rate of HSR compared to a historical control. The primary objective was the rate of HSR of any grade after the first cycle of paclitaxel. Secondary outcomes included grade of infusion reaction and incidence of severe HSR.ResultsA total of 104 patients were included for analysis in the cetirizine group and 124 in the control group. Hypersensitivity reactions occurred in 37 (16.2%) patients in the overall population, and no statistical difference was observed between groups. (13.46% vs 18.55%; p = 0.23). Numerically more grade 3-4 HSRs occurred in the control group than the treatment group (30.77% vs 69.23; p = 0.51).ConclusionsThe addition of cetirizine to paclitaxel infusions resulted in numerically lower rates of HSR and a reduction in severity of grade 3-4 HSRs. Future studies with more robust compliance data and a larger patient population would be needed to appropriately assess the efficacy of our novel treatment regimen.

评估包括大剂量西替利嗪在内的预处理方案对减少紫杉醇超敏反应的疗效:一项回顾性队列研究。
简介:超敏反应(HSR)是紫杉醇的一种已知不良反应,约有10%的患者会发生这种反应,通常发生在第一次或第二次输注药物时。在输注紫杉醇前使用皮质类固醇、组胺-1 和组胺-2 受体拮抗剂可降低 HSR 的发生率。有限的数据表明,在输注铂类药物前使用西替利嗪作为二级预防药物可降低HSR的发生率:本研究的目的是评估与历史对照组相比,新型紫杉醇超敏预防方案(包括在输注紫杉醇前12小时和6小时给予大剂量西替利嗪)对HSR发生率的影响。首要目标是紫杉醇第一周期后任何等级的HSR发生率。次要结果包括输液反应等级和严重HSR的发生率:西替利嗪组共有104名患者接受了分析,对照组共有124名患者接受了分析。总体中有 37 例(16.2%)患者发生了过敏反应,组间无统计学差异。(13.46% vs 18.55%; p = 0.23)。对照组发生 3-4 级 HSR 的人数多于治疗组(30.77% vs 69.23;p = 0.51):结论:在紫杉醇输注中添加西替利嗪可降低HSR发生率,并减轻3-4级HSR的严重程度。未来的研究需要更可靠的依从性数据和更大的患者群体,以适当评估我们的新型治疗方案的疗效。
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
2.70
自引率
7.70%
发文量
276
期刊介绍: Journal of Oncology Pharmacy Practice is a peer-reviewed scholarly journal dedicated to educating health professionals about providing pharmaceutical care to patients with cancer. It is the official publication of the International Society for Oncology Pharmacy Practitioners (ISOPP). Publishing pertinent case reports and consensus guidelines...
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