Efficacy and safety of thalidomide in preventing oral mucositis in patients with nasopharyngeal carcinoma undergoing concurrent chemoradiotherapy: A multicenter, open‐label, randomized controlled trial. Issue 7 (15th December 2021)

• Record Type: Journal Article
• Authors: Liang, Leifeng; Liu, Zhibing; Zhu, Haisheng; Wang, Hongqian; Wei, Yan; Ning, Xuejian; Shi, Zhiling; Jiang, Liujun; Lin, Zhan; Yan, Haolin; Wang, Rensheng; Hu, Kai
• Is Part Of: Cancer. Volume 128:Issue 7(2022)
• Page Start: 1467
• Page End: 1474
• Publication Date: 2021-12-15
• Subjects: concurrent chemoradiotherapy -- efficacy -- nasopharyngeal carcinoma -- oral mucositis -- safety -- thalidomide; Cancer -- Periodicals; Cancer -- Cytopathology -- Periodicals; 616.99405
• DOI: 10.1002/cncr.34074
• Languages: English
• ISSNs: 0008-543X

Abstract

Abstract : Background: This multicenter clinical trial was designed to evaluate the efficacy and safety of thalidomide (THD) in preventing oral mucositis (OM) in patients with nasopharyngeal carcinoma (NPC) undergoing concurrent chemoradiotherapy (CCRT). Methods: Patients with locally advanced NPC were randomly assigned to either a THD group or a control group. All 160 patients received radical intensity‐modulated radiotherapy plus cisplatin‐based concurrent chemotherapy and basic oral hygiene guidance. Patients in the THD group received additional THD at the beginning of CCRT. The primary end points were the latency period and the incidence of OM. The secondary end points were mouth and throat soreness (MTS), weight loss, short‐term efficacy, and adverse events. Results: The median latency period of OM was 30 and 14 days in the THD and control groups, respectively (hazard ratio, 0.32; 95% confidence interval, 0.23‐0.35; P < .0001). The incidence of OM and severe OM (World Health Organization grade 3 or higher) was significantly lower in the THD group than the control group (87.5% vs 97.5% [ P = .016] and 27.5% vs 46.3% [ P = .014], respectively). THD treatment also remarkably reduced the intensity of MTS and the degree of weight loss. In comparison with the control group, the incidence of nausea, vomiting, and insomnia was significantly decreased, whereas the incidence of dizziness and constipation was obviously increased in the THD group. The objective response rates 3 months after CCRT were similar between the groups. Conclusions: THD prolonged the latency period, reduced the incidence of OM, and did not affect the short‐term efficacy of CCRT in patients with NPC. Lay Summary: Oral mucositis is the most common complication of nasopharyngeal carcinoma during chemoradiotherapy; it decreases the patient's quality of life, and ideal mucosal protective agents are lacking. A few basic research and preclinical studies have shown that thalidomide may be an approach to ameliorating oral mucositis. The results of the current study confirm that thalidomide has a protective effect against oral mucositis in patients who have received chemoradiotherapy for nasopharyngeal carcinoma. Abstract : Thalidomide could prolong the latency period and reduce the incidence of oral mucositis in patients who have received concurrent chemoradiotherapy for nasopharyngeal carcinoma. Thalidomide administration is well tolerated and safe.