Udon Thani Cancer Hospital, Department of Medical Services, Ministry of Public Health, Thailand.
Division of Radiation Oncology, Department of Radiology, Faculty of Medicine, Chiang Mai University, Thailand.
Eur J Oncol Nurs. 2022 Aug;59:102164. doi: 10.1016/j.ejon.2022.102164. Epub 2022 Jun 17.
To assess the efficacy of topical aloe vera gel on radiation induced dermatitis (RID) in head and neck cancer (HNC) patients.
In this multicenter randomized double-blind controlled study, HNC patients treated with concurrent chemoradiation (CCRT) received either aloe vera gel or placebo gel. Adverse skin toxicity levels were evaluated with the radiation-induced skin reaction assessment scale (RISRAS).
One hundred-twenty patients were enrolled in this study. Analysis of the baseline characteristics did not reveal any differences between the groups. The median RISRAS values from the 1st to the 8th week of the CCRT course were not statistically different between the two groups. In the 5th and 6th weeks of treatment, moderate to severe grades of skin erythematous were observed at values of 13.6% and 24.1% versus 27.8 and 42.6% for members of the aloe vera gel group and the placebo group, respectively (p = 0.05 for the 5th week and p = 0.038 for the 6th week). In the 7th week, moderate to severe instances of moist desquamation were observed in eight patients (19.0%) in the placebo group (p = 0.001). Subjects experienced a burning sensation with RISRAS scores of 3-4 in the 7th week representing only 11.9% of patients in the placebo group (p = 0.016).
Topical applications of aloe vera gel significantly reduced moderate to severe grades of skin erythematous and instances of moist desquamation in HNC patients receiving CCRT. In this study, there was no prophylactic efficacy for RID in the aloe vera gel group when compared to the placebo group.
评估局部应用芦荟凝胶对头颈部癌症(HNC)患者放射性皮炎(RID)的疗效。
在这项多中心随机双盲对照研究中,接受同期放化疗(CCRT)的 HNC 患者接受芦荟凝胶或安慰剂凝胶治疗。采用放射性皮肤反应评估量表(RISRAS)评估不良反应皮肤毒性程度。
本研究共纳入 120 例患者。对基线特征的分析显示两组之间没有差异。CCRT 疗程第 1 至第 8 周的 RISRAS 中位数值在两组之间无统计学差异。在治疗的第 5 周和第 6 周,与芦荟凝胶组的 13.6%和 24.1%相比,观察到中度至重度皮肤红斑的发生率分别为 27.8%和 42.6%;而安慰剂组的发生率分别为 42.6%和 27.8%(第 5 周 p=0.05,第 6 周 p=0.038)。在第 7 周,安慰剂组中有 8 例(19.0%)患者出现中度至重度湿性脱皮(p=0.001)。在第 7 周,RISRAS 评分 3-4 分的患者出现烧灼感,安慰剂组仅占 11.9%(p=0.016)。
局部应用芦荟凝胶可显著减轻接受 CCRT 的 HNC 患者的中度至重度皮肤红斑和湿性脱皮发生率。在这项研究中,与安慰剂组相比,芦荟凝胶组对 RID 没有预防作用。