Akagi Shinsuke, Fujiwara Takashi, Nishida Mai, Okuda Akiko, Nagao Yuka, Okuda Toshikatsu, Tokuda Hidenori, Takayanagi Kazunobu
1Department of Pharmacy, Ohara Healthcare Foundation Kurashiki Central Hospital, Okayama, Japan.
2Department of Otolaryngology/Head and Neck Surgery, Ohara Healthcare Foundation Kurashiki Central Hospital, Okayama, Japan.
J Pharm Health Care Sci. 2019 Jul 25;5:16. doi: 10.1186/s40780-019-0146-2. eCollection 2019.
Oral mucositis is a frequent and severe adverse event in patients undergoing chemoradiotherapy for head and neck cancers, especially grade 3 or 4 mucositis. Occurrence may result in drop-out from treatment, thereby reducing survival. We aimed to clarify the effectiveness and safety of rebamipide mouthwash for oral mucositis in patients with head and neck cancer receiving treatment.
We carried out a systematic review and meta-analysis of patients with head and neck cancer who were treated with rebamipide mouthwash. We searched PubMed, EMBASE, and Cochrane Central Register of Controlled Trials (CENTRAL), and the World Health Organization (WHO) International Clinical Trial Registry Platform. The primary outcome was the incidence of severe oral mucositis, and secondary outcomes were time from treatment start to onset of oral mucositis, the response rate of radiotherapy, and any adverse events.
We included three studies comparing rebamipide versus placebo, all of which evaluating chemoradiotherapy induced oral mucositis. The chemotherapeutic agent was docetaxel in one study and cisplatin in the remaining two. Radiotherapy in each study consisted of 3D-conformal radiation therapy, intensity modulated radiation therapy and conventional radiation therapy, respectively. The calculated odds ratio was 0.29 [95% confidence interval (CI): 0.15 to 0.55], showing a positive association in the three studies between the incidence of grade 3-4 oral mucositis and chemotherapy for head and neck cancer. One study reported an onset of oral mucositis and the time to onset was 14.6 ± 6.4 days for the rebamipide group and 11.2 ± 4.4 days for placebo. One study reported a complete response of 8.3% for placebo and 16.7% for the rebamipide the group, and the partial response was 91.7 and 75.0%, respectively. Adverse events were reported in two studies to be 6.1 and 11.6% for placebo, and 19.4 and 26.0% in the rebamipide group, respectively.
Rebamipide mouthwash is effective in the prevention of severe mucositis and stomatitis. However, evaluation of adverse events in observational studies are needed.
口腔黏膜炎是头颈部癌症患者接受放化疗时常见且严重的不良事件,尤其是3级或4级黏膜炎。其发生可能导致患者中断治疗,进而降低生存率。我们旨在阐明瑞巴派特漱口水对头颈部癌症治疗患者口腔黏膜炎的有效性和安全性。
我们对接受瑞巴派特漱口水治疗的头颈部癌症患者进行了系统评价和荟萃分析。我们检索了PubMed、EMBASE、Cochrane对照试验中心注册库(CENTRAL)以及世界卫生组织(WHO)国际临床试验注册平台。主要结局是严重口腔黏膜炎的发生率,次要结局是从治疗开始到口腔黏膜炎发作的时间、放疗缓解率以及任何不良事件。
我们纳入了三项比较瑞巴派特与安慰剂的研究,所有研究均评估放化疗引起的口腔黏膜炎。一项研究中的化疗药物为多西他赛,其余两项为顺铂。每项研究中的放疗分别包括三维适形放疗、调强放疗和传统放疗。计算得出的比值比为0.29[95%置信区间(CI):0.15至0.55],表明三项研究中3 - 4级口腔黏膜炎的发生率与头颈部癌症化疗之间存在正相关。一项研究报告了口腔黏膜炎的发作情况,瑞巴派特组的发作时间为14.6±6.4天,安慰剂组为11.2±4.4天。一项研究报告安慰剂组的完全缓解率为8.3%,瑞巴派特组为16.7%,部分缓解率分别为91.7%和75.0%。两项研究报告的不良事件发生率,安慰剂组分别为6.1%和11.6%,瑞巴派特组分别为19.4%和26.0%。
瑞巴派特漱口水在预防严重黏膜炎和口腔炎方面有效。然而,需要在观察性研究中对不良事件进行评估。