Effects of an Indomethacin Oral Spray on Pain Due to Oral Mucositis in Cancer Patients Treated With Radiotherapy and Chemotherapy: A Double-Blind, Randomized, Placebo-Controlled Trial (JORTC-PAL04)

被引:7
作者
Nagaoka, Hiroka [1 ]
Momo, Kenji [1 ,2 ]
Hamano, Jun [1 ]
Miyaji, Tempei [3 ]
Oyamada, Shunsuke [4 ]
Kawaguchi, Takashi [5 ]
Homma, Masato [6 ]
Yamaguchi, Takuhiro [7 ]
Morita, Tatsuya [8 ]
Kizawa, Yosiyuki [9 ]
机构
[1] Univ Tsukuba, Fac Med, Div Clin Med, 1-1-1 Tennoudai, Tsukuba, Ibaraki 3058575, Japan
[2] Showa Univ, Sch Pharm, Dept Hosp Pharmaceut, Tokyo, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Clin Trial Data Management, Tokyo, Japan
[4] Tokyo Univ Pharm & Life Sci, Dept Biostat, Japanese Org Res & Treatment Canc JORTC Data Ctr, Tokyo, Japan
[5] Tokyo Univ Pharm & Life Sci, Dept Pract Pharm, Sch Pharm, Tokyo, Japan
[6] Univ Tsukuba, Fac Med, Dept Pharmaceut Sci, Tsukuba, Ibaraki, Japan
[7] Tohoku Univ, Grad Sch Med, Dept Biostat, Sendai, Miyagi, Japan
[8] Kobe Univ, Sch Med, Dept Palliat & Support Care, Palliat Care Team,Seirei Mikatagahara Gen Hosp, Kobe, Hyogo, Japan
[9] Kobe Univ, Sch Med, Dept Palliat Med, Kobe, Hyogo, Japan
关键词
Oral mucositis; indomethacin oral spray; pain control; chemotherapy; radiotherapy; CLINICAL-PRACTICE GUIDELINES; QUALITY-OF-LIFE; TOPICAL MORPHINE; HEAD; PREVENTION; MODULE;
D O I
10.1016/j.jpainsymman.2021.01.123
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Context. Oral mucositis (OM) pain due to anticancer chemo-and radiotherapy has a very negative impact on patient quality of life. However, no high-quality studies have been performed regarding the analgesic efficacy of indomethacin (IM) oral spray for OM pain. Objectives. This randomized, placebo-controlled, double-blind trial aimed to evaluate the analgesic efficacy of IM oral spray for OM pain due to anticancer chemo-and radiotherapy. Methods. From July 2015 to December 2016, we enrolled adult cancer patients with OM pain that was due to anticancer chemo-or radiotherapy and was rated 4 or higher on Brief Pain Inventory (BPI) Item 5. Patients were randomly assigned in a 1:1 ratio to receive either IM oral spray or placebo. The primary endpoint was the change in the BPI Item 6 ("current pain") score from before to 30 minutes after treatment. Secondary endpoints were the areas under the curves of BPI Item 6 at 15, 60, 120, 180, and 240 minutes after treatment; five items related to meals and conversation from the European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire, Head and Neck Module 35; the Clinical Global Impressions-Improvement (CGI-I) scale; and adverse events. Results. A total of 60 patients were assigned to receive IM oral spray (n = 33) or placebo spray (n = 27). The average change in the BPI item 6 score from before to 30 minutes after treatment was -1.85 (95% confidence interval: -2.37 to -1.32) in the IM spray group and -0.59 (-1.02 to -0.16) in the placebo group, indicating a significant difference (-1.26, -1.94 to -0.57, P < 0.01). The pain improvement persisted for 180 minutes. The intergroup differences in ability to drink liquids, ease in conversing, and CGI-I were all significant (P = 0.03, P = 0.02, and P < 0.01, respectively). No serious adverse events were reported. Conclusion. IM oral spray alleviated short-term OM pain due to anticancer chemo-and radiotherapy, and may reduce the difficulty in eating meals. (C) 2021 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:537 / 544
页数:8
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