CI

At a glance

ClinicalIndex Comparison Record
Phase 3Unknown· 122 target
Drug / intervention
G-SCFdrug
Likely dose
G-SCF 0.5 gfrom record
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Search/NCT03665480
NCT03665480Phase 3Unknown

The Effect of Granulocyte-colony Stimulating Factor (G-CSF) on Minimal Residual Disease (MRD) After Induction Therapy in Newly Diagnosed Acute Myeloid Leukemia (AML)

Nanfang Hospital, Southern Medical University·interventional·Posted Sep 11, 2018·Updated Oct 9, 2018

In Brief

A Phase 3 clinical trial evaluating G-SCF for Granulocyte Colony-stimulating Factor and 2 related conditions. Targeting 122 participants across 1 site.

Detailed Summary

Granulocyte-colony stimulating factor (G-CSF) is konwn to have no significant effect on leukemia stem cells and has been widely used in the patients with agranulocytosis after chemotherapy. Minimal residual disease (MRD), an index for early treatment response, plays an important role in prognostic prediction. Numbers of data have shown MRD at day 14 after induction therapy significantly predicts prognosis. However, the retrospetive data from the investigators showed that patients with G-CSF treatment after induction had higher MRD at day 14 but not significantly different at day 28, suggesting that G-CSF might work on the differenciation of hemapoetic stem cells and increase MRD levels at day 14. In this multicenter prospective randomized controlled study, the effect of G-CSF on MRD after induction therapy in newly diagnosed acute myeloid leukemia (AML) is evaluated.

Study Details

Timeline

Phase 3UnknownOverdue
20192020202120222023202420252026
First PostedSep 11, 2018
Enrollment StartSep 4, 2018
Primary CompletionAug 1, 2020
Study CompletionAug 1, 2021
TodayJul 1, 2026
Enrollment to primary: 1.9 yearsPosted 7.8 years ago

Interventions

G-SCFdrug

In G-CSF treatment group, all patients are treated with G-CSF at the dose of 5ug/kg pre day until neutrophil higher than 0.5 g/L or 14 days from day three after induction therapy. MRD is monitored at day 14 and 28, respectively, with flow cytometry and quantity PCR if a fusion gene is available.