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

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 <i>KRAS</i>/<i>NRAS</i>/<i>BRAF</i> 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+), <i>RAS</i> 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+, <i>RAS</i> 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.<b>Clinical trial registration:</b> NCT05253651 (ClinicalTrials.gov).

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Publication Details

Journal
Future Oncology
Published
2024-12-26
DOI
https://doi.org/10.1080/14796694.2024.2441101
Citations
14
Primary Topic
Colorectal Cancer Treatments and Studies
Type
article
Field-Weighted Citation Impact
3.96

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article

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

John H. Strickler, Yoshiaki Nakamura, Josep M. Tabernero, Volker Heinemann et al.
14 citations
Future Oncology
Colorectal Cancer Treatments and Studies
3.96
article

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

John H. Strickler, Yoshiaki Nakamura, Josep M. Tabernero, Volker Heinemann, Takayuki Yoshino, Salvatore Siena, Andrea Cercek, Jorge Ramos, Kanwal Pratap Singh Raghav, Tanios Bekaii‐Saab, Thierry André, Eric Van Cutsem, Xuesong Guan
article en
14 citations

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 <i>KRAS</i>/<i>NRAS</i>/<i>BRAF</i> 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+), <i>RAS</i> 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+, <i>RAS</i> 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.<b>Clinical trial registration:</b> NCT05253651 (ClinicalTrials.gov).

Future OncologyVol. 21(3)
Hebron University (PS), Memorial Sloan Kettering Cancer Center (US), The University of Texas MD Anderson Cancer Center (US), Pfizer (United States) (US), University of Milan (IT), Universitair Ziekenhuis Leuven (BE), WinnMed (US), LMU Klinikum (DE), Sorbonne Université (FR), Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda (IT), Hôpital Saint-Antoine (FR), Duke Medical Center (US), Vall d'Hebron Hospital Universitari (ES), Mayo Clinic Hospital (US), National Cancer Center Hospital East (JP), Scripps MD Anderson Cancer Center (US), Ludwig-Maximilians-Universität München (DE), KU Leuven (BE)
Pfizer, American Society of Clinical Oncology, Seagen, European Society for Medical Oncology, Japanese Society of Medical Oncology
Good health and well-being
Openalex Percentile: Top 5%
Colorectal Cancer Treatments and Studies
3.96
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