Show simple item record

 
dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorStrickler, John
dc.contributor.authorCercek, Andrea
dc.contributor.authorHeinemann, Volker
dc.contributor.authorNakamura, Yoshiaki
dc.contributor.authorRaghav, Kanwal
dc.contributor.authorBekaii-Saab, Tanios
dc.contributor.authorTabernero, Josep
dc.date.accessioned2025-03-06T08:50:42Z
dc.date.available2025-03-06T08:50:42Z
dc.date.issued2024-12-26
dc.identifier.citationStrickler JH, Bekaii-Saab T, Cercek A, Heinemann V, Nakamura Y, Raghav K, et al. MOUNTAINEER-03 phase III study design: first-line mFOLFOX6 + tucatinib + trastuzumab for HER2+ metastatic colorectal cancer. Futur Oncol. 2024 Dec 26;21(3):303–11.
dc.identifier.issn1744-8301
dc.identifier.urihttp://hdl.handle.net/11351/12694
dc.descriptionFirst-line treatment; Trastuzumab; Metastatic colorectal cancer
dc.description.abstractPatients 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.
dc.language.isoeng
dc.publisherTaylor & Francis
dc.relation.ispartofseriesFuture Oncology;21(3)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subjectCòlon - Càncer - Tractament
dc.subjectRecte - Càncer - Tractament
dc.subjectQuimioteràpia combinada
dc.subjectMetàstasi
dc.subjectProteïnes quinases - Inhibidors - Ús terapèutic
dc.subjectAnticossos monoclonals - Ús terapèutic
dc.subject.meshColorectal Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshNeoplasm Metastasis
dc.subject.meshProtein-Tyrosine Kinases
dc.subject.mesh/antagonists & inhibitors
dc.subject.meshAntibodies, Monoclonal
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshProgression-Free Survival
dc.titleMOUNTAINEER-03 phase III study design: first-line mFOLFOX6 + tucatinib + trastuzumab for HER2+ metastatic colorectal cancer
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1080/14796694.2024.2441101
dc.subject.decsneoplasias colorrectales
dc.subject.decs/farmacoterapia
dc.subject.decsmetástasis neoplásica
dc.subject.decsproteína-tirosina cinasas
dc.subject.decs/antagonistas & inhibidores
dc.subject.decsanticuerpos monoclonales
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada
dc.subject.decssupervivencia libre de progresión
dc.relation.publishversionhttps://doi.org/10.1080/14796694.2024.2441101
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Strickler JH] Division of Medical Oncology, Duke University Medical Center, Durham, NC, USA. [Bekaii-Saab T] Division of Hematology and Medical Oncology, Mayo Clinic, Phoenix, AZ, USA. [Cercek A] Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA. [Heinemann V] Department of Haematology and Oncology, LMU Klinikum, University of Munich, Comprehensive Cancer Center, Munich, Germany. [Nakamura Y] Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital Japan East, Kashiwa, Japan. [Raghav K] Department of Gastrointestinal Medical Oncology,MD Anderson Cancer Center, Houston, TX,USA. [Tabernero J] Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
dc.identifier.pmid39723627
dc.identifier.wos001385307700001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record