EligibleTrials

DOSAGE Study: Upfront Dose-Reduced Chemotherapy in Older Patients with Metastatic Colorectal Cancer

Recruiting · NCT06275958 · Interventional (participants receive a specific treatment) · Lead sponsor: Leiden University Medical Center

View the official record on ClinicalTrials.gov →
Colorectal Cancer

Interventions studied

Doublet Chemotherapy, Dose-reduced (75%)Doublet Chemotherapy, Standard Dose (100%)Monotherapy, Dose-reduced (75%)Monotherapy, Standard Dose (100%)

What this trial is about

The goal of this phase III, open-label, non-inferiority randomized controlled clinical trial is compare upfront dose-reduced chemotherapy with the standard dose chemotherapy in older patients ( ≥70 years) with metastasized colorectal cancer, with regard to progression-free survival (PFS). The choice between monotherapy (a fluoropyrimidine) and doublet chemotherapy (a fluoropyrimidine with oxaliplatin) will be made for each individual patient based on expected risk of chemotherapy toxicity (according to the G8 screening). Patients classified as low risk of toxicity will be randomized between doublet chemotherapy in either full-dose, or with an upfront dose-reduction of 25%. Patients classified as high risk will be randomized between monotherapy in either full-dose or upfront dose-reduction. Primary outcome is PFS. Secondary endpoints include grade ≥3 toxicity, QoL, physical functioning, overall survival, number of treatment cycles, dose reductions, hospital admissions, cumulative received dosage and cost-effectiveness.

Who can take part

Age range
70 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 3
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

36 locations listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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