[Treatment of EGFRIs-related Skin Adverse Reactions by Zhiyang Pingfu Lotion].

中国中西医结合杂志 Pub Date : 2017-02-01
Yan-Mei Peng, Hui-Juan Cui, Zhel Liu, Fang-Fang Jing, Yu-Ping Chu, Yan-Ping Bai, Dai-Wei Liu, Ya-Zhong Song, Hua Duan, Yu-Qin Qiu
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Abstract

Objective To observe the curative effect of Zhiyang Pingfu Lotion (ZPL) for its ex- ternal application in treatment of epidermal growth factor receptor inhibitors (EGFRIs)-related acneiform rash, cutaneous pruritus , xerosis cutis , and nail changes , as well as to evaluate its safety and patients' satisfaction. Methods Recruited were 201 patients with confirmed pathological diagnosis, who had acne- iform rash after using EGFRIs. They were assigned to the treatment group (131 cases) and the control group (70 cases) by random digit table. Patients in the treatment group were externally applied with self- formulated ZPL based on principles of Western medical standards, while those in the control group were externally applied with blank drugs plus conventional Western medicine standard. The therapeutic course for all was 14 days. Changes in rash degree, cutaneous pruritus, xerosis cutis, and nails were observed in both groups before and after treatment. Blood routines as well as liver and kidney function tests were performed in both groups before and after treatment. Follow-up visit was also conducted during progression-free survival (PFS). Results A total of 185 patients finished this clinical trial. Ten dropped out in the treatment group and 6 in the control group. The effective rates of rash degree, cutaneous pruritus, xerosis cutis, and nail changes were 90.1 % (109/121 ), 57.9% (70/121 ), 57. 9% (70/121 ), and 16. 5% (20/121) in the treatment group, respectively. They were 14. 1% (9/64), 6. 3% (4/64), 1. 6% (1164), and 0 (0/64) in the control group, respectively. Significant difference existed in all these indices between the two groups (X² = 105. 1022, 51. 3312, 59. 1777; P <0. 05). No serious drug-related adverse events occurred during clinical observation, with relatively better safety. The satisfaction was 95. 40% (125/131) in the treatment group and 57. 1 % (40/70) in the control group. No statistical difference in PFS was observed between the two groups (X² = 2. 006, P > 0. 05). Conclusions ZPL had significantly curative effect in treatment of EGFRIs-related skin adverse reactions, with no obvious adverse reactions. Howev- er, more randomized control trials are needed to verify these findings.

【致阳平复洗剂治疗egris相关皮肤不良反应】。
目的观察致阳平复洗剂外用治疗表皮生长因子受体抑制剂(EGFRIs)相关的痤疮样皮疹、皮肤瘙痒、皮肤干燥、指甲变化的疗效,并评价其安全性和患者满意度。方法招募201例经病理确诊,使用EGFRIs后出现痤疮样皮疹的患者。按随机数字表法分为治疗组(131例)和对照组(70例)。治疗组患者外用根据西医标准原则自行配制的ZPL,对照组患者外用空白药物加西医常规标准。治疗疗程均为14天。观察两组患者治疗前后皮疹程度、皮肤瘙痒、皮肤干燥、指甲的变化。两组患者治疗前后均行血常规及肝肾功能检查。在无进展生存期(PFS)也进行了随访。结果共185例患者完成临床试验。治疗组10例退出,对照组6例退出。皮疹程度、皮肤瘙痒、皮肤干燥、指甲改变的有效率分别为90.1%(109/121)、57.9%(70/121)、57。9%(70/121)和16。治疗组分别为5%(20/121)。他们当时14岁。1%(9/64) 6。3%(4/64), 1。对照组分别为6%(1164)和0(0/64)。两组患者各项指标比较差异均有统计学意义(X²= 105)。1022年,51。3312年,59岁。1777;P 0。05). 结论ZPL治疗egris相关皮肤不良反应疗效显著,无明显不良反应。然而,需要更多的随机对照试验来验证这些发现。
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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