A Phase 2 interventional study of bevacizumab and filgrastim in Colorectal Cancer, sponsored by Federation Francophone de Cancerologie Digestive. Completed. Open to participants aged 18 Years to 74 Years. Per ClinicalTrials.gov, last updated 2020-03-30.
Sponsored by Federation Francophone de Cancerologie Digestive · Phase 2, Interventional, and Supportive care
RATIONALE: G-CSF may prevent or control neutropenia caused by first-line therapy in patients with metastatic colorectal cancer.
PURPOSE: This phase II trial is studying how well G-CSF works in preventing neutropenia during first-line treatment with chemotherapy and bevacizumab in patients with metastatic colorectal cancer.
OBJECTIVES:
Primary
Secondary
OUTLINE: This is a multicenter study.
Patients receive bevacizumab IV over 30-90 minutes, irinotecan hydrochloride IV over 90 minutes, leucovorin calcium IV over 2 hours, and fluorouracil IV over 46 hours on day 1. Patients also receive filgrastim (G-CSF) subcutaneously on days 5-11. Treatment repeats every 2 weeks in the absence of disease progression or unacceptable toxicity.
After completion of study therapy, patients are followed every 2-3 months for up to 5 years.
5,598 studies on the registry are indexed under Colorectal Neoplasms; 1,458 are open to participants now.
This study's enrollment of 20 is below the median of 77 across 4,122 interventional studies indexed under Colorectal Neoplasms.
Browse Colorectal Neoplasms studies →Federation Francophone de Cancerologie Digestive is the lead sponsor of 61 studies on the registry; 15 are open to participants now.
Counted across the registry records on this site, refreshed daily.
DISEASE CHARACTERISTICS:
Inclusion criteria:
Histologically confirmed adenocarcinoma of the colon or rectum
Exclusion criteria:
PATIENT CHARACTERISTICS:
Inclusion criteria:
Exclusion criteria:
Active cardiac disease including any of the following:
PRIOR CONCURRENT THERAPY:
Inclusion criteria:
Exclusion criteria:
Oral or parenteral coagulant in the past 10 days and during study therapy
FOLFIRI-bévacizumab avec G-CSF en prophylaxie primaire
Biological: bevacizumab · Biological: filgrastim · Drug: fluorouracil · Drug: irinotecan hydrochloride · Drug: leucovorin calcium
Rate of neutropenia grade 4 or fever
Time frame: 2013
Toxicities by NCI-CTC v. 2.0
Time frame: 2013
Objective response at 6 months by RECIST
Time frame: 2013
Tolerance (except neutropenia) by NCI-CTC v. 2.0
Time frame: 2013
Progression-free survival
Time frame: 2013
Overall survival
Time frame: 2013
Time to treatment failure
Time frame: 2013
No study locations are listed for this record.
This study is completed, as verified in May 2016. You cannot join it, but the record below documents what was studied.
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Federation Francophone de Cancerologie Digestive