首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Topical hyaluronic acid vs. standard of care for the prevention of radiation dermatitis after adjuvant radiotherapy for breast cancer: Single-blind randomized phase III clinical trial
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Topical hyaluronic acid vs. standard of care for the prevention of radiation dermatitis after adjuvant radiotherapy for breast cancer: Single-blind randomized phase III clinical trial

机译:局部透明质酸与乳腺癌辅助放疗后预防放射性皮炎的护理标准:单盲,随机,III期临床试验

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Purpose: To determine the efficacy of an emulsion containing hyaluronic acid to reduce the development of ≥Grade 2 radiation dermatitis after adjuvant breast radiation compared with best supportive care. Methods and Materials: Women with breast cancer who had undergone lumpectomy and were to receive whole-breast radiotherapy to 50 Gy with a 10- to 16-Gy surgical bed boost were enrolled in a prospective randomized trial to compare the effectiveness of a hyaluronic acid-based gel (RadiaPlex) and a petrolatum-based gel (Aquaphor) for preventing the development of dermatitis. Each patient was randomly assigned to use hyaluronic acid gel on the medial half or the lateral half of the irradiated breast and to use the control gel on the other half. Dermatitis was graded weekly according to the Common Terminology Criteria v3.0 by the treating physician, who was blinded as to which gel was used on which area of the breast. The primary endpoint was development of ≥Grade 2 dermatitis. Results: The study closed early on the basis of a recommendation from the Data and Safety Monitoring Board after 74 of the planned 92 patients were enrolled. Breast skin treated with the hyaluronic acid gel developed a significantly higher rate of ≥Grade 2 dermatitis than did skin treated with petrolatum gel: 61.5% (40/65) vs. 47.7% (31/65) (p = 0.027). Only 1ne patient developed Grade 3 dermatitis using either gel. A higher proportion of patients had worse dermatitis in the breast segment treated with hyaluronic acid gel than in that treated with petrolatum gel at the end of radiotherapy (42% vs. 14%, p = 0.003). Conclusion: We found no benefit from the use of a topical hyaluronic acid-based gel for reducing the development of ≥Grade 2 dermatitis after adjuvant radiotherapy for breast cancer. Additional studies are needed to determine the efficacy of hyaluronic acid-based gel in controlling radiation dermatitis symptoms after they develop.
机译:目的:与最佳支持治疗相比,确定含有透明质酸的乳剂在辅助性乳房放疗后减少≥2级放射性皮炎发展的功效。方法和材料:接受过肿块切除术并接受10到16Gy手术床加重50 Gy的全乳放疗的乳腺癌妇女参加了一项前瞻性随机试验,以比较透明质酸-基凝胶(RadiaPlex)和凡士林基凝胶(Aquaphor)可预防皮炎的发展。每个患者被随机分配在被照射的乳房的内侧或外侧使用透明质酸凝胶,另一侧使用对照凝胶。治疗医师根据通用术语标准v3.0每周对皮肤炎进行分级,该医师对在乳房的哪个区域使用哪种凝胶视而不见。主要终点是≥2级皮炎。结果:在计划的92位患者中有74位患者入选后,根据数据和安全监测委员会的建议,研究提前结束。透明质酸凝胶治疗的乳房皮肤≥2级皮炎的发生率比凡士林凝胶治疗的皮肤显着更高:分别为61.5%(40/65)和47.7%(31/65)(p = 0.027)。仅使用一种凝胶的1ne患者会发展为3级皮炎。与放疗结束时用凡士林凝胶治疗的患者相比,接受透明质酸凝胶治疗的乳腺患者患皮炎的比例更高(42%vs. 14%,p = 0.003)。结论:我们发现使用局部透明质酸基凝胶减少乳腺癌辅助放疗后≥2级皮炎的发生没有益处。需要进一步的研究来确定透明质酸凝胶在发展为放射性皮炎症状后控制其功效。

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