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
Creators
- 1. Department of Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TX (United States)
- 2. Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, TX (United States)
- 3. Houston Precision Cancer Center, Houston, TX (United States)
Description
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
Availability note (English)
Available from http://dx.doi.org/10.1016/j.ijrobp.2011.09.021Additional details
Identifiers
- DOI
- 10.1016/j.ijrobp.2011.09.021;
- PII
- S0360-3016(11)03219-6;
Publishing Information
- Journal Title
- International Journal of Radiation Oncology, Biology and Physics
- Journal Volume
- 83
- Journal Issue
- 4
- Journal Page Range
- p. 1089-1094
- ISSN
- 0360-3016
- CODEN
- IOBPD3
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 44019420
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CLINICAL TRIALS; DERMATITIS; GELS; HYALURONIC ACID; MAMMARY GLANDS; MONITORING; NEOPLASMS; PATIENTS; RADIOTHERAPY; RECOMMENDATIONS; SKIN; SURGERY; SYMPTOMS; WOMEN
- Descriptors DEC
- AMINES; ANIMALS; BODY; CARBOHYDRATES; COLLOIDS; DISEASES; DISPERSIONS; FEMALES; GLANDS; MAMMALS; MAN; MEDICINE; MUCOPOLYSACCHARIDES; NUCLEAR MEDICINE; ORGANIC COMPOUNDS; ORGANS; POLYSACCHARIDES; PRIMATES; RADIOLOGY; SACCHARIDES; SKIN DISEASES; TESTING; THERAPY; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.