Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT04166604

LONsurf and G-CSF Use: Being On A Right Dose-intensity to Optimize Treatment Efficacy

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
176 (actual)
Sponsor
GERCOR - Multidisciplinary Oncology Cooperative Group · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Prospective cohort of patients treated with trifluridine/tipiracil, maximal sample size 250 patients. It is expected, that 89 patients will experience a grade 3-4 neutropenia and will be included in the phase II.

Detailed description

Trifluridine/tipiracil has demonstrated its efficacy in patients with metastatic colorectal cancer (mCRC) resistant to standard drugs (fluoropyrimidine, oxaliplatin, irinotecan, bevacizumab, and panitumumab or cetuximab in case of RAS wild-type tumors). This treatment has a marketing authorization. Neutropenia is a classic complication of cytotoxic treatments. Febrile neutropenia are associated with a mortality rate of 9.5% and a hospitalization of 6 days in median. Recent meta-analyses have reported that the use of granulocyte-colony stimulating factor (GCSF) allows to maintain the dose-intensity of cytotoxic treatment and was associated with a better overall survival (OS). There is currently no clear recommendation for the use of G-CSF with trifluridine/tipiracil. Unpublished analyses that various clinical parameters may be associated with the risk of neutropenia: age ≥ 65 years, female sex, level of leukocytes at baseline, and time of initial diagnostic to randomization ≥ 36 months.These data are too preliminary to allow proposing a G-CSF primary prophylaxis in a defined subgroup of patients. However, a secondary prophylaxis based on the administration of G-CSF seems efficient, with a prescription from day 14 to day 18. The aim of this phase II study is to assess the efficacy of the secondary prophylaxis with G-CSF in case of first episode of grade 3-4 neutropenia in the aim to maintain the optimal dose intensity.

Conditions

Interventions

TypeNameDescription
DRUGTrifluridine/TipiracilAfter morning and evening meal Days 1 through 5: 35mg/m2 (twice daily) Days 6 through 7: recovery Days 8 through 12: 35mg/m2 (twice daily) Day 13 through 28: recovery

Timeline

Start date
2020-05-20
Primary completion
2023-11-10
Completion
2025-11-01
First posted
2019-11-18
Last updated
2025-08-19

Locations

22 sites across 1 country: France

Source: ClinicalTrials.gov record NCT04166604. Inclusion in this directory is not an endorsement.