RecruitingPhase 2NCT05706779

Encorafenib Plus Cetuximab in a Neoadjuvant Setting in Patients With BRAF Mutation Localised Colon or Upper Rectum Cancer

Combination of Encorafenib Plus Cetuximab in a Neoadjuvant Setting in Patients With Braf v600e-mutates Localised Colon or Upper Rectum Cancer (Neoraf Study)


Sponsor

Federation Francophone de Cancerologie Digestive

Enrollment

30 participants

Start Date

Feb 13, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This is a pilot trial which aims to assess the concept of anti-BRAF neoadjuvant treatment (encorafenib) in combination with cetuximab in patients with colon cancer or rT3/T4 supra-peritoneal upper rectal cancer based on a pre-operative CT-scan. About 10% of patients will have a mutated BRAF V600E tumour and the objective is to include 30 patients with this mutation. If the tumour is not confirmed as a carrier of the BRAF V600E mutation or has an RAS mutation according to centralised assessment, treatment will be discontinued in this patient and cancer surgery will be organised as soon as possible. The patient will be excluded from the statistical analysis and will be replaced by a new patient in order to obtain 30 patients with confirmed BRAF V600E mutation and RAS wild type . It should be noted that less than a 3% discrepancy between the numbers of local laboratory results and central analysis results, has been reported in over 600 BRAF V600E mutated colon cancers in the BEACON CRC study. Based on these figures, there should be 0 or 1 patient with discrepant results in the study presented here. Furthermore, in the hypothetical case of a patient who is an early permanent discontinuation of the study prior to surgery, this patient will be replaced in order to obtain a total of 30 patients who underwent surgery after neoadjuvant treatment.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of two targeted drugs — encorafenib and cetuximab — given before surgery (neoadjuvant treatment) in patients with locally advanced colon or upper rectal cancer that has a specific mutation called BRAF V600E. The goal is to shrink the tumor before surgery to improve outcomes. **You may be eligible if...** - You are 18 or older - You have been diagnosed with colon or upper rectal adenocarcinoma confirmed by biopsy - Your tumor has a BRAF V600E mutation - Your cancer is localized and considered removable with surgery, with significant spread into surrounding tissue (T3 with >5 mm extension, or T4) - Your blood counts, kidney, and liver function meet acceptable ranges - Your heart function is normal (no prolonged QT interval) **You may NOT be eligible if...** - You have a RAS mutation in addition to BRAF V600E - Your cancer has spread to distant sites - You have serious heart, kidney, or liver problems - You have uncontrolled skin conditions or eye problems that could be worsened by these drugs Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGEncorafenib Oral Capsule + Cetuximab

Encorafenib: 4 capsules 75 mg/day (300 mg) , 7 days/7 during 6 weeks Cetuximab: 500mg/m2 intravenous route every 2 weeks (D1, D14, D28), for 3 cycles over 4 weeks.


Locations(1)

Chu - Hôpital Européen Georges Pompidou

Paris, France

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NCT05706779


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