Primary and Acquired Resistance to Targeted Treatment in BRAF V600E-mutated Metastatic Colorectal Cancer
Primary and Acquired Resistance to Targeted Treatment in BRAF V600E-mutated Metastatic Colorectal Cancer (PARTACER-Suisse)
Swiss Cancer Institute
30 participants
May 25, 2025
OBSERVATIONAL
Conditions
Summary
This study prospectively investigates the molecular mechanisms of primary and acquired resistance to standard-of-care BRAF V600E-directed therapy in patients with metastatic colorectal cancer and aims to pre-clinically develop novel strategies to reverse therapy resistance. Clinically approved combination treatment with cetuximab, encorafenib and chemotherapy improves patient outcomes, yet patients eventually experience disease progression. In this prospective multicenter study, tumor tissue, blood, and stool samples will be collected before treatment and at progression, to identify genetic and non-genetic mechanisms of resistance. Additionally, tumor tissue-based in vitro models (patient-derived organoids, PDOs) will be generated and exploited for functional in vitro testing, including genomic and pharmacologic perturbation studies. The overarching goal is to generate knowledge that can help develop new and more effective treatment strategies for future patients.
Eligibility
Inclusion Criteria8
- Diagnosis of unresectable or metastatic BRAF V600E-mutated colorectal cancer
- Planned initiation of treatment with combined anti-EGFR antibody and BRAF inhibitor
- Patients receiving treatment in any line, with or without chemotherapy
- At least one tumor lesion accessible for biopsy
- ECOG performance status 0-2
- Life expectancy of at least 3 months
- Age ≥18 years
- Ability to provide written informed consent
Exclusion Criteria5
- Medical or surgical contraindication for tumor biopsy
- Active second malignancy (except non-melanoma skin cancer)
- Inability to comply with study procedures (e.g., due to language barriers or cognitive impairment)
- Pregnancy or breastfeeding
- Previous treatment with a BRAF inhibitor
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Interventions
Longitudinal translational sampling (tumor tissue, plasma ctDNA, stool, PBMCs).
Locations(12)
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NCT07617610