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一项随机临床试验,研究局部应用聚普瑞锌预防造血干细胞移植患者口腔黏膜炎(ToPaZ 研究)。

A randomised trial of topical polaprezinc to prevent oral mucositis in patients undergoing haematopoietic stem cell transplantation (ToPaZ study).

机构信息

Pharmacy Department, Royal Brisbane and Women's Hospital, Brisbane, Australia.

School of Pharmacy, The University of Queensland, Brisbane, Australia.

出版信息

Support Care Cancer. 2023 Dec 19;32(1):44. doi: 10.1007/s00520-023-08235-y.

Abstract

PURPOSE

Oral mucositis (OM) is a common complication in haematopoietic stem cell transplantation (HSCT). Polaprezinc, an anti-ulcer drug, has been shown to be effective to prevent OM in several studies when administered topically and systemically. This study aimed to evaluate the effectiveness of topical polaprezinc in patients undergoing HSCT.

METHODS

This was an open-label randomised clinical trial comparing polaprezinc and sodium bicarbonate mouthwashes for the prevention of severe OM in HSCT patients. Adult patients who received conditioning regimens at moderate to high risk of developing OM were included. The primary endpoint was the incidence of severe (WHO grades 3-4) OM. The secondary endpoints included duration of grades 3-4 OM, incidence and duration of grades 2-4 OM, patient-reported pain and functional limitations.

RESULTS

In total, 108 patients (55 test arm and 53 control arm) were randomised. There was no difference in the incidence of grades 3 to 4 OM (35% test arm versus 36% control arm). The secondary endpoints were not significantly different. In both arms, patients reported more throat pain compared to mouth pain.

CONCLUSIONS

Topical polaprezinc had no effect in the prevention of OM in HSCT patients. Further research is required to evaluate the effects of systemic polaprezinc. The OM assessment tool needs to be reviewed as throat mucositis was a main issue in this study.

TRIAL REGISTRATION

ACTRN12320001188921 (Date Registered: 10th November 2020).

摘要

目的

口腔黏膜炎(OM)是造血干细胞移植(HSCT)的常见并发症。聚普瑞锌是一种抗溃疡药物,多项研究表明,局部和全身给药均可有效预防 OM。本研究旨在评估 HSCT 患者中局部应用聚普瑞锌的效果。

方法

这是一项开放标签随机临床试验,比较了聚普瑞锌和碳酸氢钠漱口液在预防 HSCT 患者重度 OM 中的作用。纳入接受中高危致 OM 预处理方案的成年患者。主要终点为重度(WHO 3-4 级)OM 的发生率。次要终点包括 3-4 级 OM 的持续时间、2-4 级 OM 的发生率和持续时间、患者报告的疼痛和功能受限。

结果

共纳入 108 例患者(试验组 55 例,对照组 53 例)。3-4 级 OM 的发生率在两组间无差异(试验组 35%,对照组 36%)。次要终点也无显著差异。两组患者均报告喉咙疼痛较口腔疼痛更为严重。

结论

局部应用聚普瑞锌对 HSCT 患者 OM 的预防无作用。需要进一步研究评估全身应用聚普瑞锌的效果。需要对 OM 评估工具进行评估,因为在这项研究中,喉咙黏膜炎是一个主要问题。

临床试验注册号

ACTRN12320001188921(注册日期:2020 年 11 月 10 日)。

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