4.0 Article

Effect of Nano-Curcumin on Radiotherapy-Induced Skin Reaction in Breast Cancer Patients: A Randomized, Triple-Blind, Placebo-Controlled Trial

Journal

CURRENT RADIOPHARMACEUTICALS
Volume 15, Issue 4, Pages 332-340

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1874471015666220623104316

Keywords

Breast cancer; radiation therapy; radiation-induced skin reaction; nano-curcumin; clinical trial; RTOG scale

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This study aimed to evaluate the efficacy of nano-curcumin in alleviating radiation-induced skin reactions (RISRs) in breast cancer patients. The results showed that the administration of nano-curcumin could alleviate radiation-induced skin toxicity, although the effect was not significant.
Purpose: Despite advances in medical technology, radiation-induced dermatitis occurs in 95% of cancer patients receiving radiation therapy. Currently, there is no standard and effective treatment for the prevention or control of radiation dermatitis. The aim of this study was to determine the efficacy of nano-curcumin in alleviating the radiation-induced skin reactions (RISRs) in breast cancer patients. Methods: A randomized, triple-blinded, placebo-controlled clinical trial was performed on 42 patients with breast cancer. The patients were randomly allocated to receive radiotherapy plus placebo (control group) and radiotherapy plus 80 mg/day nano-curcumin capsules (treatment group) up to two weeks after the end of treatment. Then, the RISRs (graded by the radiation therapy oncology group (RTOG) scale) and pain level of the patients were evaluated at baseline and weekly. Finally, the results were analyzed by T-test and Pearson chi-square test. Results: According to the RTOG scale, 0%, 14.28%, and 85.71% of patients in the control group showed grades 0, 1, and 2 RISRs, respectively. In the treatment group, it was observed that 9.52%, 47.61%, and 42.85% of patients had grades 0, 1, and 2 RISRs, respectively. Compared to the control group, it was found that concomitant use of the nano-curcumin supplement did not significantly reduce the RISR severity during the first to sixth weeks (P > 0.05); however, there was a significant difference at week 7 (P = 0.01). Moreover, the patient-reported pain, as the secondary endpoint, was significantly reduced in the treatment group compared with the control group (P < 0.05). Conclusions: In general, it was found that the administration of nano-curcumin could alleviate radiation-induced skin toxicity of breast cancer patients, but this effect was not significant.

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