Clinical implications of FLT3 mutations in pediatric AML

Soheil Meshinchi, Todd A. Alonzo, Derek L. Stirewalt, Michel Zwaan, Martin Zimmerman, Dirk Reinhardt, Gertjan J.L. Kaspers, Nyla A. Heerema, Robert Gerbing, Beverly J. Lange, Jerald P. Radich

Onderzoeksoutput: Bijdrage aan tijdschriftArtikelpeer review

308 Citaten (Scopus)

Samenvatting

Activating mutations of the FLT3 gene occur because of an internal tandem duplication of the juxta-membrane domain (FLT3/ITD) or point mutation of the activation loop domain (FLT3/ALM). The presence of FLT3 mutations as well as the allelic ratio of FLT3/ITD (ITD-AR, mutant-wild type ratio) may have prognostic significance. FLT3 mutation status of 630 children with de novo acute myeloid leukemia (AML) treated on CCG-2941 and -2961 was determined, and ITD-AR was calculated for patients with FLT3/ITD. Clinical characteristics and outcomes for patients with FLT3/ALM and FLT3/ITD at varying ITD-ARs was determined and compared with those without FLT3 mutations (FLT3/WT). FLT3/ITD and FLT3/ALM were detected in 77 (12%) and 42 (6.7%) of the patients. Progression-free survival (PFS) was similar in patients with FLT3/ ALM and FLT3/WT (51% versus 55%, P = .862). In contrast, PFS at 4 years from study entry for patients with FLT3/ITD was inferior to that of patients with FLT3/WT (31% versus 55%, P < .001). PFS decreased with increasing FLT3/ITD-AR (P < .001), and those with ITD-AR greater than 0.4 had a significantly worse PFS than those with lower ITD-AR (16% versus 72%, P = .001) or with FLT3/WT (55%, P < .001). ITD-AR defines the prognostic significance in FLT3/ITD-positive AML, and ITD-AR greater than 0.4 is a significant and independent prognostic factor for relapse in pediatric AML.

Originele taal-2Engels
Pagina's (van-tot)3654-3661
Aantal pagina's8
TijdschriftBlood
Volume108
Nummer van het tijdschrift12
DOI's
StatusGepubliceerd - 1 dec. 2006
Extern gepubliceerdJa

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