首页> 外文期刊>Journal of Cancer >The clinical impact of Hangeshashinto (TJ-14) in the treatment of chemotherapy-induced oral mucositis in gastric cancer and colorectal cancer: Analyses of pooled data from two phase II randomized clinical trials (HANGESHA-G and HANGESHA-C)
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The clinical impact of Hangeshashinto (TJ-14) in the treatment of chemotherapy-induced oral mucositis in gastric cancer and colorectal cancer: Analyses of pooled data from two phase II randomized clinical trials (HANGESHA-G and HANGESHA-C)

机译:Hangeshashinto(TJ-14)在胃癌和大肠癌化疗诱导的口腔粘膜炎的治疗中的临床效果:来自两项II期随机临床试验(HANGESHA-G和HANGESHA-C)的汇总数据分析

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Background : The current pooled analysis evaluated the efficacy of Hangeshashinto (TJ-14) in the prevention and/or treatment of chemotherapy-induced oral mucositis (COM) in gastric cancer and colorectal cancer using two prospective, multi-institutional, randomized, double-blind, placebo-controlled phase II trials. Patients and Methods : HANGESHA-G and HANGESHA-C randomly assigned patients with gastric cancer or colorectal cancer who developed moderate to severe COM (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 four to six weeks, according to the chemotherapy regimen, from the start of their next course of chemotherapy. The primary endpoint was the incidence of grade ≥2 COM in the protocol treatment course, and the secondary endpoints were the time to disappearance of COM and the incidence of adverse events. Results : The pooled population included 181 patients. The incidence of grade ≥2 COM in the TJ-14 group was 55.7% (49 patients), while that in the placebo group was 53.8% (50 patients); there was no significant difference between the two groups (p=0.796). The median time to remission of grade ≥2 COM to grade <1 was 8 days in the TJ-14 group and 15 days in the placebo group (p= 0.072). The hazard ratio was 1.54 [1.02 to 2.31] in favor of TJ-14. Treatment with TJ-14 was associated with marginally significant reduction in the duration of severe grade ≥2 COM in comparison to patients receiving placebo indicating the effect of TJ-14 in reducing the severity of COM. Conclusion: The present-pooled analysis showed that TJ-14 had a treatment effect in gastric cancer and colorectal cancer patients with COM in comparison to a placebo. Further phase III studies with a larger sample size are needed to clarify the protective effects of TJ-14 against COM. This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
机译:背景:目前的汇总分析使用两种前瞻性,多机构,随机,双重研究方法评估了Hangeshashinto(TJ-14)在预防和/或治疗胃癌和结肠直肠癌的化学疗法诱发的口腔粘膜炎(COM)中的功效。盲目的,安慰剂对照的II期临床试验。患者和方法:HANGESHA-G和HANGESHA-C随机分配在任何化疗周期中发展为中度至重度COM(≥1级)的胃癌或大肠癌患者,以TJ-14或安慰剂作为双盲治疗试用。根据化疗方案,患者从下一个化疗疗程开始接受安慰剂或TJ-14,持续4至6周。主要终点是方案治疗过程中≥2级COM的发生率,次要终点是COM消失的时间和不良事件的发生率。结果:合并人群包括181例患者。 TJ-14组≥2级COM的发生率为55.7%(49例),而安慰剂组为53.8%(50例)。两组之间无显着差异(p = 0.796)。在TJ-14组中,≥2 COM缓解至<1级的中位缓解时间为8天,而安慰剂组为15天(p = 0.072)。 TJ-14的危险比为1.54 [1.02至2.31]。与接受安慰剂的患者相比,TJ-14的治疗与严重≥2级COM的持续时间显着降低有关,这表明TJ-14可以降低COM的严重程度。结论:目前的分析表明,与安慰剂相比,TJ-14对胃癌和大肠癌的COM患者有治疗作用。需要进一步进行具有更大样本量的III期研究,以阐明TJ-14对COM的保护作用。这是根据知识共享署名(CC BY-NC)许可(https://creativecommons.org/licenses/by-nc/4.0/)的条款分发的开放获取文章。有关完整的条款和条件,请参见http://ivyspring.com/terms。

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