Department of Surgery, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Department of Breast and Endocrine surgery, National Hospital Organization Nagasaki Medical Center, Nagasaki, Japan.
J Evid Based Dent Pract. 2023 Sep;23(3):101896. doi: 10.1016/j.jebdp.2023.101896. Epub 2023 Jun 11.
No standard approach other than oral care is available for preventing chemotherapy-induced stomatitis in patients with breast cancer. In this randomized, controlled phase 2 trial, we aimed to assess the efficacy and safety of a dexamethasone-based mouthwash in preventing chemotherapy-induced stomatitis in patients with early breast cancer.
Patients with breast cancer scheduled for epirubicin and cyclophosphamide (EC) or docetaxel and cyclophosphamide (TC) therapy were selected and allocated in a 1:1 ratio to the intervention and control groups. The intervention group received chemotherapy, oral care, and a dexamethasone-based mouthwash, whereas the control group received chemotherapy and oral care. The primary endpoint was the incidence of stomatitis. This was a phase 2 study, and the significance level for the analysis of the primary endpoint was set a priori at 0.2.
Data pertaining to 58 patients in the control group and 59 patients in the intervention group were analyzed. Stomatitis incidence was 55% and 38% in the control and intervention groups, respectively (risk ratio, 0.68; 80% confidence interval, 0.52-0.88; P = .052). Stomatitis severity was lower in the intervention group than in the control group (P = .03). The proportion of patients who adhered to the mouthwash regimen was 87% (interquartile range, 67.8%-95.3%). No severe oral infections were observed.
The dexamethasone-based mouthwash safely reduced stomatitis incidence and severity in patients receiving chemotherapy for early breast cancer. Phase 3 clinical trials are warranted for validating our results.
除了口腔护理外,目前尚无标准方法可用于预防乳腺癌患者的化疗引起的口腔炎。在这项随机对照的 2 期试验中,我们旨在评估基于地塞米松的漱口水预防早期乳腺癌患者化疗引起的口腔炎的疗效和安全性。
选择计划接受表柔比星和环磷酰胺(EC)或多西他赛和环磷酰胺(TC)治疗的乳腺癌患者,并按 1:1 的比例随机分配到干预组和对照组。干预组接受化疗、口腔护理和基于地塞米松的漱口水,而对照组仅接受化疗和口腔护理。主要终点是口腔炎的发生率。这是一项 2 期研究,对主要终点进行分析的显著性水平预先设定为 0.2。
对对照组的 58 例患者和干预组的 59 例患者的数据进行了分析。对照组和干预组的口腔炎发生率分别为 55%和 38%(风险比,0.68;80%置信区间,0.52-0.88;P=0.052)。干预组的口腔炎严重程度低于对照组(P=0.03)。接受漱口水方案治疗的患者比例为 87%(四分位距,67.8%-95.3%)。未观察到严重的口腔感染。
基于地塞米松的漱口水可安全降低接受早期乳腺癌化疗的患者口腔炎的发生率和严重程度。需要进行 3 期临床试验来验证我们的结果。