局部替马洛尔预防化疗相关口腔黏膜炎:一项前瞻性随机、双盲、安慰剂对照的癌症患者临床试验。

IF 1.2 Q4 PHARMACOLOGY & PHARMACY
Fatemeh Saghafi, Fatemeh Shaker-Ardakani, Mohsen Nabi-Meybodi, Hassan-Ali Vahedian-Ardakani, Adeleh Sahebnasagh
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引用次数: 0

摘要

背景:替马洛尔是一种β -肾上腺素能阻滞剂,已被证明对伤口愈合有效。口腔黏膜炎(OM)是口腔黏膜的一种急性炎症,是一些化疗方案引起口腔黏膜溃疡的令人烦恼的副作用。目前的研究旨在评估噻洛尔漱口水对接受化疗的成年患者的OM预防作用,并与安慰剂进行比较。方法:对30例接受阿霉素或5-氟尿嘧啶(5-FU)化疗方案的成人患者进行随机、双盲试验。患者按1:1的比例随机分配,接受0.5%替莫洛尔(w/v) (n = 15)或安慰剂(n = 15)漱口水,每次5毫升,每天3次。研究的结果是在研究期间的7周内,每周根据世界卫生组织(WHO)粘膜炎量表评估OM的强度和基于视觉模拟量表(VAS)评估OM相关疼痛。结果:研究结果显示,与对照组相比,替洛尔组在研究第1周期间WHO粘膜炎评分显著降低[周均值(SD),替洛尔组为0.02(0.41),对照组为0.67 (0.48);第7周:平均(SD),替莫洛尔组0.33(0.61),对照组0.87 (0.74);p值= 0.049]。替洛尔组患者第1、2、3周的平均疼痛评分较对照组明显降低(p值< 0.05)。结论:本初步临床试验结果表明,在接受阿霉素或5-FU化疗方案的患者中,在7周的随访期间,预防性使用噻洛尔漱口水与对照组相比,明显减轻了OM的严重程度。在研究的前三周,疼痛的严重程度也明显降低;然而,效应量小于最小临床重要差异。需要进一步的研究来评估噻莫洛尔漱口水预防OM的长期疗效和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevention of Chemotherapy-related Oral Mucositis by Topical Timolol: A Prospective Randomized, Double-blind, Placebo-controlled Clinical Trial in Cancer Patients.

Background: Timolol is a beta-adrenergic blocker that has been shown to be effective in the healing of wounds. Oral mucositis (OM), an acute inflammation of the oral mucosa, is a bothersome side effect of some regimens of chemotherapy in which the oral mucosa becomes ulcerated. The current study aimed to evaluate the prophylactic effects of timolol mouthwash in preventing OM in adult patients receiving chemotherapy compared to the placebo.

Method: This randomized, double-blind trial was conducted on 30 adult patients receiving chemotherapy regimen, including doxorubicin or 5-fluorouracil (5-FU). The patients were randomized in a 1:1 ratio to receive either timolol 0.5% (w/v) (n = 15) or placebo (n = 15) mouthwash 5 ml three times per day. The outcomes of the study were the intensity of OM evaluated by the World Health Organization (WHO) mucositis scale and OM-related pain based on the Visual Analog Scale (VAS) weekly during the seven weeks of the study period.

Results: The results of the study showed that the scores of WHO mucositis scale significantly decreased in the timolol group compared to the control group during the study [week 1: mean (SD), 0.02 (0.41) in the timolol group, and 0.67 (0.48) in the control group; week 7: mean (SD), 0.33 (0.61) in the timolol group, and 0.87 (0.74) in the control group; P-value = 0.049]. Moreover, the mean pain scores significantly decreased in the first, second, and third weeks in the timolol group compared to the control group (P-value < 0.05).

Conclusion: The results of this preliminary clinical trial demonstrated that among the patients receiving doxorubicin or 5-FU chemotherapy regimens, the preventive use of timolol mouthwash significantly diminished the severity of OM compared to the control group during the seven weeks of follow-up. The severity of pain was also significantly lower during the first three weeks of the study; however, the effect size was less than the minimal clinically important difference. Further studies are required to assess both the long-term efficacy and safety of timolol mouthwash in preventing OM.

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CiteScore
4.30
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