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三药联合标准止吐方案中添加或不添加 5 毫克奥氮平预防蒽环类/环磷酰胺方案治疗乳腺癌患者化疗所致恶心呕吐的双盲、对照、随机日本临床试验方案(JTOP-B)。

Study protocol for a double-blind, comparative, randomised Japanese trial of triplet standard antiemetic therapies with or without 5 mg olanzapine to prevent chemotherapy-induced nausea and vomiting for patients with breast cancer treated with an anthracycline/cyclophosphamide regimen (JTOP-B).

机构信息

Department of Breast Oncology, Juntendo University School of Medicine, Tokyo, Japan.

Department of Pharmacy, Gifu University Hospital, Gifu, Japan

出版信息

BMJ Open. 2022 Mar 2;12(3):e058755. doi: 10.1136/bmjopen-2021-058755.

Abstract

INTRODUCTION

Triple antiemetic therapy with neurokinin-1 receptor antagonist, 5-hydroxytryptamine type 3 receptor antagonist, and dexamethasone has been widely recommended for high emetogenic chemotherapeutic (HEC) agents and regimens, including anthracycline combined with cyclophosphamide (AC). The addition of olanzapine (OLZ) 5 mg or 10 mg to the recommended triple antiemetic therapy has demonstrated superiority in antiemetic efficacy compared with the standard triplet therapy for a cisplatin-based HEC regimen. Although OLZ plus the triple antiemetic treatment may also be effective for patients on an AC-based HEC regimen, no study has investigated its efficacy at a lower dose of 5 mg.

METHODS AND ANALYSIS

To assess whether 5 mg OLZ, as compared with placebo, in combination with triple combination therapy, significantly improves nausea and vomiting, we are conducting a randomised, parallel-group controlled clinical trial with a total of 500 patients at 15 study centres in Japan. The primary outcome is the complete response rate, defined as no emetic episodes and no use of rescue medication during 120 hours after the initiation of chemotherapy. Treatment group comparison for the primary endpoint will be done by using the Cochran-Mantel-Haenszel test.

ETHICS AND DISSEMINATION

The study was approved by the institutional review board of Juntendo University Hospital and relevant approval was obtained from all participating centres. All participants will be required to provide written informed consent. The trial results will be reported at conferences and in peer-reviewed journals.

TRIAL REGISTRATION NUMBER

Japan Registry of Clinical Trials (jRCT) jRCT1031200134; protocol date: 30 July 2020, version: 1.3, approval: 25 August 2020.

摘要

简介

神经激肽-1 受体拮抗剂、5-羟色胺 3 受体拮抗剂和地塞米松的三联止吐疗法已被广泛推荐用于高致吐性化疗药物(HEC)药物和方案,包括蒽环类药物联合环磷酰胺(AC)。与标准三联疗法相比,奥氮平(OLZ)5 毫克或 10 毫克联合推荐的三联止吐疗法在止吐疗效方面表现出优越性,适用于顺铂为基础的 HEC 方案。尽管 OLZ 加三联止吐治疗可能对接受基于 AC 的 HEC 方案的患者也有效,但尚无研究调查其 5 毫克低剂量的疗效。

方法和分析

为了评估与安慰剂相比,5 毫克 OLZ 联合三联联合疗法是否能显著改善恶心和呕吐,我们正在日本的 15 个研究中心对 500 名患者进行一项随机、平行组对照临床试验。主要结局是完全缓解率,定义为化疗开始后 120 小时内无呕吐发作且无使用解救药物。将使用 Cochran-Mantel-Haenszel 检验对主要终点的治疗组进行比较。

伦理和传播

该研究已获得顺天堂大学医院机构审查委员会的批准,并从所有参与中心获得了相关批准。所有参与者都将需要提供书面知情同意书。试验结果将在会议和同行评议期刊上报告。

试验注册编号

日本临床试验注册(jRCT)jRCT1031200134;方案日期:2020 年 7 月 30 日,版本:1.3,批准日期:2020 年 8 月 25 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/8896054/74f604d0cb98/bmjopen-2021-058755f01.jpg

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