Institut Gustave Roussy, Villejuif, France.
Centre Hospitalier de Bretagne Sud, Lorient, France.
Int J Radiat Oncol Biol Phys. 2017 Nov 1;99(3):590-595. doi: 10.1016/j.ijrobp.2017.07.019. Epub 2017 Jul 22.
Concomitant cetuximab and radiation therapy (RT) can induce severe radiodermatitis in patients with head and neck cancer (HNC). OTD70DERM, a regenerating agent (RGTA), is a structural and functional analogue of glycosaminoglycans. Preclinical studies have shown that topical RGTA can markedly reduce radiation-induced mucosal and cutaneous toxicities without tumor protection. The present study aimed to evaluate the effect of topical RGTA on radiodermatitis in patients with HNC undergoing RT and cetuximab, for whom RT-induced skin reactions are frequent and/or severe. The primary endpoint was the incidence of grade ≥2 radiodermatitis.
We performed a multicenter, randomized, double-blind, placebo-controlled trial of patients with newly diagnosed HNC undergoing conventionally fractionated RT (70 Gy in 35 fractions) and weekly cetuximab. Patients were randomized 1:1 to receive topical OTD70DERM or placebo on irradiated skin once daily. The National Cancer Institute Common Terminology Criteria for Adverse Events, version 3.0, was used to evaluate radiodermatitis (photographs of radiation zone). The Dermatology Life Quality Index score was also evaluated. All the skin reactions seen on the photographs were scored independently by 2 outside experts.
Of the 76 randomized patients (38 in each arm), 72 were available for the final radiodermatitis evaluation (37 in the RGTA arm and 35 in the placebo arm). No significant difference was observed concerning the incidence or duration of grade ≥2 radiodermatitis between the 2 arms (81% for RGTA vs 80% for placebo; P=.9). Also, no significant difference was found between the 2 arms regarding grade ≥2 radiodermatitis evaluated by the 2 experts using the photographs of 68 patients (76% vs 74%; P=.78). Finally, no significant difference was found in the Dermatology Life Quality Index score (score >10, 15% vs 20%; P=.45).
Despite the good preclinical rationale, RGTA did not reduce the incidence and severity of radiodermatitis in patients with HNC.
曲妥珠单抗联合放射治疗(RT)可导致头颈部癌症(HNC)患者发生严重放射性皮炎。OTD70DERM 是一种再生剂(RGTA),是糖胺聚糖的结构和功能类似物。临床前研究表明,局部 RGTA 可显著减轻放射性粘膜和皮肤毒性,而不具有肿瘤保护作用。本研究旨在评估曲妥珠单抗联合放射治疗的头颈部癌症患者中,局部 RGTA 对放射性皮炎的影响,这些患者的 RT 诱导皮肤反应频繁且/或严重。主要终点是 2 级及以上放射性皮炎的发生率。
我们进行了一项多中心、随机、双盲、安慰剂对照试验,纳入了新诊断为头颈部癌症的患者,这些患者接受常规分割 RT(70Gy 分 35 次)和每周曲妥珠单抗治疗。患者按 1:1 随机接受局部 OTD70DERM 或安慰剂,每天一次涂于照射皮肤。采用美国国立癌症研究所不良事件通用术语标准,版本 3.0,评估放射性皮炎(照射区域照片)。还评估了皮肤病生活质量指数评分。2 位外部专家独立评估照片上可见的所有皮肤反应。
76 名随机患者(每组 38 名)中,72 名患者可进行最终的放射性皮炎评估(RGTA 组 37 名,安慰剂组 35 名)。两组间 2 级及以上放射性皮炎的发生率或持续时间无显著差异(RGTA 组为 81%,安慰剂组为 80%;P=.9)。此外,使用 68 名患者的照片评估 2 位专家的 2 级及以上放射性皮炎时,两组间也未发现差异(76%对 74%;P=.78)。最后,皮肤病生活质量指数评分无显著差异(评分>10,15%对 20%;P=.45)。
尽管有良好的临床前依据,但 RGTA 并未降低头颈部癌症患者放射性皮炎的发生率和严重程度。