MOUNTAINEER-03 phase III study design: first-line mFOLFOX6 + tucatinib + trastuzumab for HER2+ metastatic colorectal cancer.

IF 3 4区 医学 Q2 ONCOLOGY
Future oncology Pub Date : 2025-02-01 Epub Date: 2024-12-26 DOI:10.1080/14796694.2024.2441101
John H Strickler, Tanios Bekaii-Saab, Andrea Cercek, Volker Heinemann, Yoshiaki Nakamura, Kanwal Raghav, Salvatore Siena, Josep Tabernero, Eric Van Cutsem, Takayuki Yoshino, Jorge Ramos, Xuesong Guan, Thierry Andre
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Abstract

Patients diagnosed with metastatic colorectal cancer (mCRC) have a poor prognosis with survival ranging 2-3 years. The prevalence of human epidermal growth factor receptor 2 (HER2) amplification is approximately 3-4% in mCRC and increases up to 8% in patients with KRAS/NRAS/BRAF wild-type (WT) CRC tumors. Tucatinib is a highly selective HER2-directed tyrosine kinase inhibitor that, in combination with trastuzumab, has demonstrated clinically meaningful activity in patients with chemotherapy-refractory, HER2-positive (HER2+), RAS WT mCRC in the MOUNTAINEER trial. The MOUNTAINEER-03 phase III trial is designed to investigate the efficacy and safety of first-line tucatinib in combination with trastuzumab and modified FOLFOX6 (mFOLFOX6) versus standard of care (mFOLFOX6 plus bevacizumab or cetuximab) in patients with untreated HER2+, RAS WT locally advanced unresectable or mCRC. MOUNTAINEER-03 will include two arms of approximately 400 patients randomized 1:1 to either treatment arm. The primary endpoint is progression-free survival per RECIST v1.1 by blinded independent central review (BICR). Key secondary endpoints are overall survival and confirmed objective response rate (according to RECIST v1.1 per BICR). Safety assessments will include surveillance and recording of adverse events, physical examination findings, vital signs, cardiac assessments, Eastern Cooperative Oncology Group performance status, concomitant medications, and laboratory tests.Clinical trial registration: NCT05253651 (ClinicalTrials.gov).

mountainer -03 III期研究设计:一线mFOLFOX6 +图卡替尼+曲妥珠单抗治疗HER2阳性转移性结直肠癌。
诊断为转移性结直肠癌(mCRC)的患者预后较差,生存期为2-3年。人表皮生长因子受体2 (HER2)扩增在mCRC中的流行率约为3-4%,在KRAS/NRAS/BRAF野生型(WT) CRC肿瘤患者中增加高达8%。图卡替尼是一种高选择性HER2导向的酪氨酸激酶抑制剂,与曲妥珠单抗联合使用,在MOUNTAINEER试验中已显示出对化疗难治性HER2阳性(HER2+) RAS WT mCRC患者有临床意义的活性。mountainer -03 III期试验旨在研究一线图卡替尼联合曲妥珠单抗和改良FOLFOX6 (mFOLFOX6)与标准护理(mFOLFOX6 +贝伐单抗或西妥昔单抗)在未经治疗的HER2+、RAS WT局部晚期不可切除或mCRC患者中的疗效和安全性。MOUNTAINEER-03将包括两组约400名患者,以1:1的比例随机分配到任一治疗组。主要终点是通过盲法独立中心评价(BICR)的RECIST v1.1无进展生存期。关键次要终点是总生存期和确定的客观缓解率(根据RECIST v1.1 / BICR)。安全性评估将包括不良事件的监测和记录、体格检查结果、生命体征、心脏评估、东部肿瘤合作小组的工作状态、伴随用药和实验室检查。临床试验注册:NCT05253651 (ClinicalTrials.gov)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Future oncology
Future oncology ONCOLOGY-
CiteScore
5.40
自引率
3.00%
发文量
335
审稿时长
4-8 weeks
期刊介绍: Future Oncology (ISSN 1479-6694) provides a forum for a new era of cancer care. The journal focuses on the most important advances and highlights their relevance in the clinical setting. Furthermore, Future Oncology delivers essential information in concise, at-a-glance article formats - vital in delivering information to an increasingly time-constrained community. The journal takes a forward-looking stance toward the scientific and clinical issues, together with the economic and policy issues that confront us in this new era of cancer care. The journal includes literature awareness such as the latest developments in radiotherapy and immunotherapy, concise commentary and analysis, and full review articles all of which provide key findings, translational to the clinical setting.
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