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UnknownNCT03600558

Efficacy of FLAG Regimen for the Treatment of Patients With AML

Efficacy of Fludarabine, Cytarabine and G-CSF (FLAG Regimen) for the Treatment of Patients With Acute Myeloid Leukemia (AML)

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Tianjin Medical University General Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The long-term efficacy of chemotherapy in patients with acute myeloid leukemia (AML) has been significantly improved in recent years. The combination of anthracycline plus cytarabine (Ara-C) has been a standard induction regimen for patients with AML. However, the optimal consolidation therapy after induction chemotherapy has not reached a consensus. The FLAG regimen consisting of fludarabine and high-dose cytarabine combined with G-CSF which is one of the first-line consolidation treatment options for relapsed and refractory AML. This study conducted a retrospective analysis of the intensive treatment of AML with the FLAG regimen from January 2007 to May 2018 in our hospital to evaluate the efficacy of the FLAG regimen. To provide the basis for the choice and timing of treatment for patients with AML treated with the FLAG regimen.

Conditions

Timeline

Start date
2018-11-21
Primary completion
2020-07-01
Completion
2020-07-01
First posted
2018-07-26
Last updated
2020-04-24

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03600558. Inclusion in this directory is not an endorsement.

Efficacy of FLAG Regimen for the Treatment of Patients With AML (NCT03600558) · Clinical Trials Directory