Department of Clinical Research Design and Evaluation, SAIHST, Sungkyunkwan University, Seoul, 06351, South Korea.
Center for Clinical Epidemiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, 06351, South Korea.
Support Care Cancer. 2020 Apr;28(4):1829-1837. doi: 10.1007/s00520-019-04982-z. Epub 2019 Jul 23.
This study aimed to evaluate the impact of a topical lotion (CG428) on hair thickness and density in breast cancer survivors with permanent chemotherapy-induced alopecia (PCIA).
The study was a double-blind, randomized controlled trial which conducted from February 2016 to December 2016 at the Samsung Comprehensive Cancer Center in Seoul, South Korea. Breast cancer patients with PCIA were randomized on average of 3.5 years after chemotherapy. Topical lotion (Batch DT023) is a botanical drug under development containing a novel patented blend of 4 botanical ingredients: citrus, cocoa, guarana, and onion. Participants were asked to self-apply the study product or placebo twice per day for 6 months. Changes in hair density and thickness were assessed using a noninvasive bioengineering device, and patient-reported outcomes were evaluated at 3 and 6 months after randomization.
A total of 35 patients were randomized to intervention (N = 18) or placebo (N = 17). Patients in the intervention group were older than those in the placebo group (52.1 vs. 41.6 years; P < 0.001). The mean hair density (SD) at baseline was 97.6 (6.4) and 126.8 (30.3) hairs/cm in the intervention and placebo group, respectively (P = 0.005). The corresponding values for hair thickness were 49.9 (12.7) and 48.1 (8.4) μm, respectively. After 6 months, hair density had increased by 34.7 and 24.9% compared with baseline in the intervention and control groups, respectively (P = 0.37). Corresponding values for hair thickness were 19.8 and 35.6%, respectively (P = 0.23). Similar findings were observed after age adjustment.
In this pilot randomized clinical trial, we observed safety, tolerability, and a trend toward the efficacy of CG428 vs. placebo, especially regarding hair density and self-reported improvement.
本研究旨在评估一种局部用乳液(CG428)对患有永久性化疗诱导性脱发(PCIA)的乳腺癌幸存者头发厚度和密度的影响。
这是一项双盲、随机对照试验,于 2016 年 2 月至 2016 年 12 月在韩国首尔三星综合癌症中心进行。在化疗后平均 3.5 年随机选择 PCIA 的乳腺癌患者。局部用乳液(Batch DT023)是一种正在开发中的植物药,含有一种新颖的专利混合 4 种植物成分:柑橘、可可、瓜拉那和洋葱。参与者被要求每天使用研究产品或安慰剂两次,持续 6 个月。使用非侵入性生物工程设备评估头发密度和厚度的变化,并在随机分组后 3 个月和 6 个月评估患者报告的结果。
共有 35 名患者被随机分配至干预组(N=18)或安慰剂组(N=17)。干预组患者比安慰剂组患者年龄更大(52.1 岁比 41.6 岁;P<0.001)。干预组和安慰剂组的基线时头发密度(SD)分别为 97.6(6.4)和 126.8(30.3)根/cm(P=0.005)。相应的头发厚度值分别为 49.9(12.7)和 48.1(8.4)μm。6 个月后,干预组和对照组的头发密度与基线相比分别增加了 34.7%和 24.9%(P=0.37)。相应的头发厚度值分别为 19.8%和 35.6%(P=0.23)。在年龄调整后也观察到类似的发现。
在这项小型随机临床试验中,我们观察到 CG428 的安全性、耐受性以及与安慰剂相比的疗效趋势,尤其是在头发密度和自我报告的改善方面。