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Association details:
Evidence:
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

Poor outcome of pediatric patients with acute myeloid leukemia harboring high FLT3/ITD allelic ratios

Published date:
06/27/2022
Excerpt:
CONTRADICTING EVIDENCE: Here, we present the outcome and prognostic significance of FLT3/ITD AR analysis among pediatric patients with AML from the TARGET dataset....our subgroup analysis demonstrated that the high AR FLT3/ITD patients who received consolidation chemotherapy plus GO (n = 21), had an inferior 5-year EFS (16.7% (37%) vs. 57.1% (55.1%), P = 0.023; Fig. 6C) and OS (25.6% (39.7%) vs. 71.4% (46.6%), P = 0.014; Fig. 6D) compared to those with SCT plus GO (n = 14).
Secondary therapy:
Chemotherapy
DOI:
10.1038/s41467-022-31489-9
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

ADDITION OF ANTI-CD33 MONOCLONAL ANTIBODY GEMTUZUMAB OZOGAMICIN TO FLAI INDUCTION SIGNIFICANTLY IMPROVES OUTCOME IN PATIENT AFFECTED BY FLT3-ITD MUTATED ACUTE MYELOID LEUKEMIA

Published date:
05/14/2020
Excerpt:
This effect was more evident among the 33 NPM1wt/FLT3-ITD patients: in this subgroup, patients who received GO had an overall good outcome, similar to those double mutated (median OS not reached in both groups, p=n.s.)...our data seem to indicate that  GO added to an intensive fludarabine/high dose ARA-C  based induction, provides a significant improvement of anti-leukemic activity in patients carrying FLT3-ITD mutation, especially if NPM1wt.
Evidence Level:
Sensitive: D – Preclinical
Source:
Title:

Addition of the Anti-CD33 Monoclonal Antibody Mylotarg to Fludarabine/High Dose Cytarabine - Based Induction Significantly Improves Outcome in Patient Affected By FLT3-ITD Positive Cytogenetically Normal Acute Myeloid Leukemia

Published date:
11/06/2019
Excerpt:
...a significant positive effect on survival among FLT3-ITD patients (3-year OS 66.7% vs 46.6% for FLT3-ITD patients receiving or not MY, respectively, p<0.03, Fig. 1). This effect was more evident among the 33 NPM1 negative/FLT3-ITD patients: in this subgroup, patients who received MY had an overall good outcome
DOI:
10.1182/blood-2019-131420