RecruitingNCT07617610

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)


Sponsor

Swiss Cancer Institute

Enrollment

30 participants

Start Date

May 25, 2025

Study Type

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

Min Age: 18 Years

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

OTHERLongitudinal translational sampling

Longitudinal translational sampling (tumor tissue, plasma ctDNA, stool, PBMCs).


Locations(12)

Kantonsspital Aarau

Aarau, Switzerland

Kantonsspital Baden

Baden, Switzerland

St. Claraspital

Basel, Switzerland

Universitaetsspital Basel

Basel, Switzerland

Inselspital Bern

Bern, Switzerland

Kantonsspital Graubünden

Chur, Switzerland

Luzerner Kantonsspital

Lucerne, Switzerland

HOCH Health Ostschweiz - Kantonsspital St. Gallen

Sankt Gallen, Switzerland

Bürgerspital Solothurn

Solothurn, Switzerland

HFR Freiburg - Kantonsspital

Villars-sur-Glâne, Switzerland

Kantonsspital Winterthur

Winterthur, Switzerland

Universitätsspital Zürich USZ

Zurich, Switzerland

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NCT07617610


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