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头颈部癌症患者接受放化疗时,预防放射性皮炎的局部皮质类固醇与安慰剂的 3 期随机试验。

Phase 3 Randomized Trial of Topical Steroid Versus Placebo for Prevention of Radiation Dermatitis in Patients With Head and Neck Cancer Receiving Chemoradiation.

机构信息

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Sunto-gun, Japan.

Department of Radiation Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

出版信息

Int J Radiat Oncol Biol Phys. 2021 Nov 1;111(3):794-803. doi: 10.1016/j.ijrobp.2021.05.133. Epub 2021 Jun 6.

Abstract

PURPOSE

Radiation dermatitis is one of the most common acute toxicities induced by chemoradiation therapy (CRT) for head and neck cancer (HNC). The benefit of topical steroids in the management of radiation dermatitis is still unclear. This phase 3, multi-institutional, randomized, double-blind, placebo-controlled trial evaluated the efficacy and safety of topical steroids for radiation dermatitis in patients with locally advanced HNC receiving CRT.

METHODS AND MATERIALS

Eligible patients were scheduled to receive bilateral neck irradiation (≥66 Gy) with concurrent cisplatin (≥200 mg/m) as definitive or postoperative CRT. Patients were randomly assigned to receive either topical steroid or placebo when grade 1radiation dermatitis was observed or the total radiation dose reached 30 Gy. Basic skin care including gentle washing and moistening in the head and neck region was performed in both groups. The primary endpoint was the frequency of grade ≥2 radiation dermatitis, in accordance with the National Cancer Institute Common Terminology Criteria for Adverse Events, version 4.0. Grading of radiation dermatitis was performed by independent central review using photographs taken weekly.

RESULTS

A total of 211 patients were enrolled (intention to treat: steroid 101 and placebo 102). The frequency of grade ≥2 radiation dermatitis was not significantly reduced with the steroid (73.3%; 95% confidence interval, 64.6%-81.9%) compared with the placebo (80.4%; 95% confidence interval, 72.7%-88.1%; P = .23), whereas the steroid significantly reduced the frequency of grade ≥3 radiation dermatitis (13.9% vs 25.5%; P = .034). No significant differences in adverse events, including local infection or compliance with CRT, were observed between the groups.

CONCLUSIONS

Topical steroid may reduce the severity of radiation dermatitis in patients with HNC and thus may become an important therapeutic tool in the management of radiation dermatitis.

摘要

目的

放射性皮炎是头颈部癌症(HNC)患者接受放化疗(CRT)后最常见的急性毒性之一。局部应用皮质类固醇在放射性皮炎治疗中的益处尚不清楚。这项多中心、随机、双盲、安慰剂对照的 3 期临床试验评估了局部应用皮质类固醇治疗接受 CRT 的局部晚期 HNC 患者放射性皮炎的疗效和安全性。

方法和材料

符合条件的患者计划接受双侧颈部照射(≥66 Gy),同时给予顺铂(≥200 mg/m)作为确定性或术后 CRT。当观察到 1 级放射性皮炎或总放射剂量达到 30 Gy 时,患者被随机分配接受局部皮质类固醇或安慰剂治疗。两组患者均接受基础皮肤护理,包括头部和颈部区域的温和清洗和保湿。主要终点是根据国家癌症研究所不良事件通用术语标准,第 4.0 版评估的 2 级及以上放射性皮炎的发生率。每周拍摄照片,由独立的中央审查机构进行放射性皮炎分级。

结果

共纳入 211 例患者(意向治疗:皮质类固醇 101 例,安慰剂 102 例)。与安慰剂组(80.4%;95%置信区间,72.7%-88.1%)相比,皮质类固醇组(73.3%;95%置信区间,64.6%-81.9%)2 级及以上放射性皮炎的发生率无显著降低(P=0.23),而皮质类固醇组显著降低了 3 级及以上放射性皮炎的发生率(13.9%比 25.5%;P=0.034)。两组间不良事件(包括局部感染或 CRT 依从性)无显著差异。

结论

局部应用皮质类固醇可能会减轻 HNC 患者放射性皮炎的严重程度,因此可能成为放射性皮炎治疗的重要治疗工具。

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