Complex Approach to the Management of Acneiform Rash Induced by Epidermal Growth Factor Receptor Inhibitors

L. S. Kruglova, E. A. Shatokhina, A. S. Polonskaia
{"title":"Complex Approach to the Management of Acneiform Rash Induced by Epidermal Growth Factor Receptor Inhibitors","authors":"L. S. Kruglova, E. A. Shatokhina, A. S. Polonskaia","doi":"10.15690/vramn10927","DOIUrl":null,"url":null,"abstract":"Rationale. Acneiform (papulopustular) rash is the leading dermatological adverse event of EGFR inhibitors. The development of optimal regimens for the supportive treatment of acneiform rash remains an important interdisciplinary problem in supportive oncology. Aims — to comparatively evaluate the clinical efficacy of the supportive treatment for acneiform rash induced by epidermal growth factor receptor inhibitors, including topical treatment with ivermectin cream and balneotherapy. Methods. In an open, prospective, randomized study, data from 114 patients with acneiform rash induced by monoclonal antibodies to EGFR were analyzed. All groups received intermittent supportive treatment according to a single regimen, continuous external therapy included: in group 1 — hypotonic thermal water, in group 2 — ivermectin 1% cream, in group 3 — hypotonic thermal water and ivermectin 1% cream. The observation period was 3 months. Acneiform rash severity was assessed using the CTCAE-NCI v5.0 criteria and a developed acneiform rash clinical severity scale. The intensity of subjective symptoms was assessed using a 10-point visual analog scale (VAS). The modified dermatological life quality index (mDLQI) was used to assess the impact of acneiform rash on patient’s quality of life. Results. A significant decrease in all of the studied parameters was observed in the groups by the end of the 1st week of supportive treatment and remained up to the end of the observation period (p 0.05). There were no statistically significant differences between groups 2 and 3 with respect to the acneiform rash clinical severity scale, but their values were significantly lower than those of group 1 (group 1 vs. group 2, p 0.001; group 1 vs. group 3, p 0.001). The most rapid resolution of all subjective symptoms was observed in group 3. Significantly lower mDLQI values were also observed in group 3 starting from the 1st week of supportive treatment until the end of the follow-up period (р 0.05). No severe adverse reactions were registered in any of the groups during the study. Conclusions. The developed regimens for the supportive treatment of acneiform rash have demonstrated a high efficacy in resolving papulopustular rash and associated subjective symptoms. The use of a complex approach including continuous topical therapy with ivermectin cream and hypotonic thermal water leads to the resolution of rash and relief of subjective symptoms in the shortest time, allows to safely maintain the achieved clinical effect for a long period of observation, has the most significant positive impact on the quality of life of cancer patients.","PeriodicalId":178392,"journal":{"name":"Annals of the Russian academy of medical sciences","volume":"4 10","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-02-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of the Russian academy of medical sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15690/vramn10927","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Rationale. Acneiform (papulopustular) rash is the leading dermatological adverse event of EGFR inhibitors. The development of optimal regimens for the supportive treatment of acneiform rash remains an important interdisciplinary problem in supportive oncology. Aims — to comparatively evaluate the clinical efficacy of the supportive treatment for acneiform rash induced by epidermal growth factor receptor inhibitors, including topical treatment with ivermectin cream and balneotherapy. Methods. In an open, prospective, randomized study, data from 114 patients with acneiform rash induced by monoclonal antibodies to EGFR were analyzed. All groups received intermittent supportive treatment according to a single regimen, continuous external therapy included: in group 1 — hypotonic thermal water, in group 2 — ivermectin 1% cream, in group 3 — hypotonic thermal water and ivermectin 1% cream. The observation period was 3 months. Acneiform rash severity was assessed using the CTCAE-NCI v5.0 criteria and a developed acneiform rash clinical severity scale. The intensity of subjective symptoms was assessed using a 10-point visual analog scale (VAS). The modified dermatological life quality index (mDLQI) was used to assess the impact of acneiform rash on patient’s quality of life. Results. A significant decrease in all of the studied parameters was observed in the groups by the end of the 1st week of supportive treatment and remained up to the end of the observation period (p 0.05). There were no statistically significant differences between groups 2 and 3 with respect to the acneiform rash clinical severity scale, but their values were significantly lower than those of group 1 (group 1 vs. group 2, p 0.001; group 1 vs. group 3, p 0.001). The most rapid resolution of all subjective symptoms was observed in group 3. Significantly lower mDLQI values were also observed in group 3 starting from the 1st week of supportive treatment until the end of the follow-up period (р 0.05). No severe adverse reactions were registered in any of the groups during the study. Conclusions. The developed regimens for the supportive treatment of acneiform rash have demonstrated a high efficacy in resolving papulopustular rash and associated subjective symptoms. The use of a complex approach including continuous topical therapy with ivermectin cream and hypotonic thermal water leads to the resolution of rash and relief of subjective symptoms in the shortest time, allows to safely maintain the achieved clinical effect for a long period of observation, has the most significant positive impact on the quality of life of cancer patients.
表皮生长因子受体抑制剂诱发痤疮样皮疹的复杂治疗方法
理由。痤疮样皮疹(丘疹脓疱)是表皮生长因子受体抑制剂的主要皮肤不良反应。为痤疮样皮疹的支持性治疗制定最佳方案仍然是支持性肿瘤学中一个重要的跨学科问题。目的--比较评估表皮生长因子受体抑制剂诱发的痤疮样皮疹的支持性治疗的临床疗效,包括伊维菌素乳膏的局部治疗和浴疗法。治疗方法在一项开放性、前瞻性、随机研究中,分析了114名表皮生长因子受体单克隆抗体诱发痤疮样皮疹患者的数据。所有组别均按照单一方案接受间歇性支持治疗,持续性外部治疗包括:第1组--低渗温泉水,第2组--1%伊维菌素软膏,第3组--低渗温泉水和1%伊维菌素软膏。观察期为 3 个月。痤疮样皮疹严重程度采用 CTCAE-NCI v5.0 标准和开发的痤疮样皮疹临床严重程度量表进行评估。主观症状强度采用 10 点视觉模拟量表(VAS)进行评估。改良皮肤病生活质量指数(mDLQI)用于评估痤疮样皮疹对患者生活质量的影响。结果显示在支持性治疗第一周结束时,观察组的所有研究参数都有明显下降,并一直保持到观察期结束(P 0.05)。在痤疮样皮疹临床严重程度量表方面,第 2 组和第 3 组之间没有明显的统计学差异,但其数值明显低于第 1 组(第 1 组对第 2 组,P 0.001;第 1 组对第 3 组,P 0.001)。第 3 组所有主观症状的缓解速度最快,而且从支持治疗的第一周开始到随访期结束,第 3 组的 mDLQI 值也明显降低(р 0.05)。研究期间,各组均未出现严重不良反应。结论所开发的痤疮样皮疹支持性治疗方案在缓解丘疹脓疱型皮疹及相关主观症状方面疗效显著。使用伊维菌素乳膏和低渗热水进行持续局部治疗的复合方法能在最短时间内消除皮疹和缓解主观症状,并能在长期观察期间安全地维持已取得的临床效果,对癌症患者的生活质量具有最显著的积极影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信