Efficacy of Epigallocatechin-3-Gallate in Preventing Dermatitis in Patients With Breast Cancer Receiving Postoperative Radiotherapy A Double-Blind, Placebo-Controlled, Phase 2 Randomized Clinical Trial

被引:28
|
作者
Zhao, Hanxi [1 ,2 ]
Zhu, Wanqi [1 ,2 ]
Zhao, Xianguang [1 ,2 ]
Li, Xiaolin [1 ,2 ]
Zhou, Zhengbo [3 ]
Zheng, Meizhu [3 ]
Meng, Xiangjiao [1 ,2 ]
Kong, Lingling [1 ,2 ]
Zhang, Shuyu [4 ]
He, Dan [4 ]
Xing, Ligang [1 ,2 ]
Yu, Jinming [1 ,2 ]
机构
[1] Shandong First Med Univ & Shandong Acad Med Sci, Shandong Canc Hosp & Inst, Dept Radiat Oncol, 440 Jiyan Rd, Jinan 250117, Shandong, Peoples R China
[2] Shandong First Med Univ & Shandong Acad Med Sci, Shandong Canc Hosp & Inst, Shandong Key Lab Radiat Oncol, Jinan, Shandong, Peoples R China
[3] Shandong First Med Univ & Shandong Acad Med Sci, Shandong Canc Hosp & Inst, Dept Breast Surg, Jinan, Shandong, Peoples R China
[4] China Natl Nucl Corp, Affiliated Hosp 2, Chengdu Med Coll, Hosp 416, Chengdu, Peoples R China
基金
中国国家自然科学基金;
关键词
ACUTE SKIN TOXICITY; ACUTE RADIATION DERMATITIS; 20-YEAR FOLLOW-UP; GREEN TEA; PROPHYLACTIC AGENT; CREAM; IRRADIATION; THERAPY; EGCG; (-)-EPIGALLOCATECHIN-3-GALLATE;
D O I
10.1001/jamadermatol.2022.1736
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
IMPORTANCE Safe and effective prophylactic therapies for radiation-induced dermatitis (RID) remain an unmet need. OBJECTIVE To determine if epigallocatechin-3-gallate (EGCG) solution reduces the incidence of RID in patients undergoing radiotherapy after breast cancer surgery. DESIGN, SETTING, AND PARTICIPANTS This phase 2 double-blind, placebo-controlled randomized clinical trial enrolled 180 patients with breast cancer receiving postoperative radiotherapy at Shandong Cancer Hospital and Institute in Shandong, China, between November 2014 and June 2019. Data analysis was performed from September 2019 to January 2020. INTERVENTIONS Participants were randomly assigned (2:1) to receive either EGCG solution (660 mu mol/L) or placebo (0.9% NaCl saline) sprayed to the whole radiation field from day 1 of the radiation until 2 weeks after radiation completion. MAIN OUTCOMES AND MEASURES The primary end point was incidence of grade 2 or worse RID, defined by the Radiation Therapy Oncology Group scale. The secondary end points included RID index (RIDI), symptom index, changes in the skin temperature measured by infrared thermal images, and safety. RESULTS A total of 180 eligible patients were enrolled, of whom 165 (EGCG, n = 111; placebo, n = 54) were evaluable for efficacy (median [range] age, 46 [26-67] years). The occurrence of grade 2 or worse RID was significantly lower (50.5%; 95% CI, 41.2%-59.8%) in the EGCG group than in the placebo group (72.2%; 95% CI, 60.3%-84.1%) (P = .008). The mean RIDI in the EGCG group was significantly lower than that in the placebo group. Furthermore, symptom indexes were significantly lower in patients receiving EGCG. Four patients (3.6%) had adverse events related to the EGCG treatment, including grade 1 pricking skin sensation (3 [2.7%]) and pruritus (1 [0.9%]). CONCLUSIONS AND RELEVANCE In this randomized clinical trial, prophylactic use of EGCG solution significantly reduced the incidence and severity of RID in patients receiving adjuvant radiotherapy for breast cancer. It has the potential to become a new choice of skin care for patients receiving radiotherapy.
引用
收藏
页码:779 / 786
页数:8
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