Last updated on July 2019
Quality of Life in Elderly Patients With Metastatic Colorectal Cancer Receiving First-line Therapy Based on Simplified Geriatric Parameters
Brief description of study
A national, multicenter, open-label, randomized phase III study. The trial aim is to determine the best therapeutic strategies according with the HRQoL.
Detailed Study Description
Treatment cohort will be determined based on three parameters:
- Serum albumin level at baseline,
- ECOG Performance Status,
- Mini GDS.
The "Candidate" group will be defined according to (all the following criteria must be fulfilled):
- Serum albumin level 30g/L,
- ECOG PS 0-1 (whatever mini GDS score) or ECOG PS 2 with mini GDS 0 (ie, no depression).
The "Non-candidate" cohort group will be defined according to (at least one of those parameters is fulfilled):
- Serum albumin level < 30g/L.
- And/ or ECOG PS 2 and mini GDS 1 (ie, depression).
Patients in the "Candidate group" will be randomized to:
- OPTIMOX bevacizumab (arm A),
- Capecitabine + bevacizumab (arm B), in priority followed by FOLFOX-bevacizumab at first progression.
Patients in the "Non-candidate" group cohort
- Not randomized, follow-up patients receiving: capecitabine + bevacizumab
Clinical Study Identifier: NCT03828227