Kim Eun Hye, Park Su Bin, Jin Hayun, Chung Weon Kuu, Yoon Seong Woo
Department of Clinical Korean Medicine, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
Department of Korean Internal Medicine, Kyung Hee University Hospital at Gangdong, Seoul, Republic of Korea.
Front Pharmacol. 2023 Jul 3;14:1216668. doi: 10.3389/fphar.2023.1216668. eCollection 2023.
Radiation-induced dermatitis (RID) is one of the most prevalent side-effects of conventional cancer therapies; however, there is no standard treatment for its prevention. Therefore, this study aimed to evaluate the comparative efficacy and safety of Jaungo (mainly composed of Siebold & Zucc. and (Oliv.) Diel) and the water-in-oil-type non-steroidal moisturizer for the prevention of RID in patients with breast cancer (BC). This is a prospective, single-blind, pilot randomized controlled trial. Between March 2021 and July 2022, 50 patients were randomly selected to use Jaungo or the moisturizer while undergoing postoperative radiation therapy (RT). Assessments were conducted nine times-every week while the patients underwent RT and 2 weeks after the end of therapy. The primary outcome was the incidence rate of RID grade ≥2. The secondary outcomes were the incidence rate of maximum grade RID, time to RID onset, RID-related quality of life (QOL) score, pain intensity, and adverse events. The incidence rate of RID grade ≥2 was 24.0% and 20.0% in the Jaungo and the moisturizer groups, respectively, with no significant difference between the groups ( = 0.733). Regarding the secondary outcomes, the incidence rate of maximum grade RID ( = 0.890), mean time to RID onset ( = 0.092), cumulative incidence rate of RID ( = 0.280), RID-related QOL score, and maximum pain intensity ( = 0.844) also did not differ significantly between the groups. None of the subjects in either group experienced severe adverse effects, although one participant in the moisturizer group had mild fever and insomnia. These findings suggest that Jaungo has preventive efficacy without severe side-effects against RID in patients with BC that is comparable to that of the water-in-oil type non-steroidal moisturizer. Further extensive randomized controlled trials with larger sample sizes are warranted to validate our findings. Clinical Research Information Service (CRIS), https://cris.nih.go.kr, identifier KCT0005971.
放射性皮炎(RID)是传统癌症治疗中最常见的副作用之一;然而,目前尚无预防其发生的标准治疗方法。因此,本研究旨在评估姜黄膏(主要由光果甘草和光果甘草(Oliv.)Diel组成)与油包水型非甾体保湿剂在预防乳腺癌(BC)患者放射性皮炎方面的相对疗效和安全性。这是一项前瞻性、单盲、试点随机对照试验。在2021年3月至2022年7月期间,随机选取50例患者在接受术后放疗(RT)时使用姜黄膏或保湿剂。在患者接受放疗期间每周进行一次评估,共评估九次,并在治疗结束后2周进行评估。主要结局是≥2级放射性皮炎的发生率。次要结局包括最高级放射性皮炎的发生率、放射性皮炎发病时间、放射性皮炎相关生活质量(QOL)评分、疼痛强度和不良事件。姜黄膏组和保湿剂组≥2级放射性皮炎的发生率分别为24.0%和20.0%,两组之间无显著差异(P = 0.733)。关于次要结局,最高级放射性皮炎的发生率(P = 0.890)、放射性皮炎发病的平均时间(P = 0.092)、放射性皮炎的累积发生率(P = 0.280)、放射性皮炎相关生活质量评分以及最大疼痛强度(P = 0.844)在两组之间也无显著差异。两组均无受试者出现严重不良反应,尽管保湿剂组有一名参与者出现轻度发热和失眠。这些发现表明,姜黄膏在预防乳腺癌患者放射性皮炎方面具有预防效果且无严重副作用,与油包水型非甾体保湿剂相当。有必要进行进一步的大样本量广泛随机对照试验以验证我们的研究结果。临床研究信息服务(CRIS),https://cris.nih.go.kr,标识符KCT0005971。