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TJ-14(汉方甘草酸制剂)治疗胃癌化疗所致口腔黏膜炎的双盲、安慰剂对照、随机 II 期研究。

Double-blind, placebo-controlled, randomized phase II study of TJ-14 (hangeshashinto) for gastric cancer chemotherapy-induced oral mucositis.

机构信息

Department of Surgery, Miura City Hospital, Miura, Japan,

出版信息

Cancer Chemother Pharmacol. 2014 May;73(5):1047-54. doi: 10.1007/s00280-014-2440-x. Epub 2014 Mar 21.


DOI:10.1007/s00280-014-2440-x
PMID:24652604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4000413/
Abstract

BACKGROUND: Hangeshashinto (TJ-14, a Kampo medicine), which reduces the level of prostaglandin E2 and affects the cyclooxygenase activity, alleviates chemotherapy-induced oral mucositis (COM). We conducted a randomized comparative trial to investigate whether TJ-14 prevents and controls COM in patients with gastric cancer. METHODS: We randomly assigned patients with gastric cancer who developed moderate-to-severe oral mucositis (CTCAE v4.0 grade ≧1) during any cycle of chemotherapy to receive either TJ-14 or a placebo as a double-blind trial. The patients received a placebo or TJ-14 for 2-6 weeks according to the chemotherapy regimen from the beginning of the next course of chemotherapy. The primary end point was the incidence of grade ≧2 oral mucositis in the protocol treatment course, and the secondary end points were the time to disappearance of oral mucositis and the incidence of adverse events. RESULTS: Following the key opening of the blinding protocol, we analyzed 91 eligible patients (TJ-14: 45, placebo: 46) using a "per protocol set" analysis. The incidence of ≧grade 2 COM was 40.0 % in the TJ-14 group and 41.3 % in the placebo group (p = 0.588). The median duration of ≧grade 2 COM was 14 days in the TJ-14 group and 16 days in the placebo group (p = 0.894). Meanwhile, the median duration of any grade of COM was 9 days in the TJ-14 group and 17 days in the placebo group among the patients who developed grade 1 symptoms during the screening cycle [hazard ratio 0.60; 95 % CI (0.23-1.59), p = 0.290]. CONCLUSIONS: Although TJ-14 treatment did not reduce the incidence of ≥2 COM in the patients who developed mucositis during chemotherapy for gastric cancer, a trend was observed in which TJ-14 reduced the risk of COM in the patients who developed grade 1 COM during the screening cycle. Further, phase III studies with a larger sample size are needed to clarify the protective effects of TJ-14 for COM.

摘要

背景:汉方制剂痛立止(TJ-14,一种汉方药)可降低前列腺素 E2 水平并影响环氧化酶活性,从而缓解化疗引起的口腔黏膜炎(COM)。我们进行了一项随机对照试验,以研究 TJ-14 是否可预防和控制胃癌患者的 COM。

方法:我们将在任何化疗周期中出现中重度口腔黏膜炎(CTCAE v4.0 分级≥1)的胃癌患者随机分为 TJ-14 组或安慰剂组,进行双盲试验。患者从下一疗程开始,根据化疗方案接受 2-6 周的安慰剂或 TJ-14 治疗。主要终点是方案治疗疗程中出现≥2 级口腔黏膜炎的发生率,次要终点是口腔黏膜炎消退时间和不良事件的发生率。

结果:在揭盲方案的关键节点后,我们对 91 例符合条件的患者(TJ-14 组 45 例,安慰剂组 46 例)进行了“符合方案集”分析。TJ-14 组的≥2 级 COM 发生率为 40.0%,安慰剂组为 41.3%(p=0.588)。TJ-14 组的≥2 级 COM 中位持续时间为 14 天,安慰剂组为 16 天(p=0.894)。同时,在筛查周期出现 1 级症状的患者中,TJ-14 组任何级别 COM 的中位持续时间为 9 天,安慰剂组为 17 天[风险比 0.60;95%CI(0.23-1.59),p=0.290]。

结论:尽管 TJ-14 治疗并未降低胃癌化疗期间发生黏膜炎的患者≥2 级 COM 的发生率,但 TJ-14 治疗在筛查周期发生 1 级 COM 的患者中降低了 COM 风险,存在降低 COM 发生率的趋势。还需要更大样本量的 III 期研究来明确 TJ-14 对 COM 的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55cf/4000413/b2d40285ec20/280_2014_2440_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55cf/4000413/28986689a967/280_2014_2440_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55cf/4000413/b2d40285ec20/280_2014_2440_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55cf/4000413/28986689a967/280_2014_2440_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55cf/4000413/b2d40285ec20/280_2014_2440_Fig2_HTML.jpg

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