Efficacy of Melatonin Oral Gel in Reducing Oral Mucositis in Patients with Head and Neck Cancer under Chemoradiation
DOI:
https://doi.org/10.30683/1929-2279.2025.14.21Keywords:
Melatonin, Oral mucositis, Head and neck cancer, ChemoradiationAbstract
Objective: Oral Mucositis is a significant burden for patients receiving radiation treatment for head and neck cancer. This study aimed to evaluate the efficacy of melatonin oral gel in reducing radiation induced oral mucositis.
Patients and methods: This is prospective, randomized clinical controlled study including locally advanced head and neck cancer patients receiving chemoradiation. The selected participants were recruited into two groups (40 individuals each). Group 1 (melatonin group) will receive 20 mg/ 10 ml /twice per day melatonin gel mouth wash, along with the conventional treatment. Group 2 (control group) will receive conventional treatment only. All participants were evaluated by oral mucositis scale and visual analog scale for pain. Reduced glutathione was quantitated using GSH Colorimetric Assay Kit at base line and on the last day of treatment.
Results: All patients in both treatment groups had low-grade mucositis (grade 1–2). After two weeks, 30% of the patients in the control group had developed severe mucositis (grade 3–4), meanwhile this grade was not reported in melatonin group. At the end of study, 80% of the cases had severe mucositis in the control group compared to the melatonin group (10%) with p value 0.001. At the end of each week, the mean values of pain score were significantly lower in melatonin arm compared to control arm. Also, the mean level of salivary GSH significantly increased in both groups(39.5 ± 2.7 and 29.2 ± 3.85) for the melatonin and control groups, respectively as compared to the baseline value and there were statistically significant differences in Favor to melatonin group (group I; P= 0.001).
Conclusion: Oral mucositis is a clinically critical consequence of chemoradiation. Melatonin significantly reduces pain and irradiation induced mucositits through oncostatic and cytoprotective mechanisms.
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