Is the Prenatal Origin of Acute Myeloid Leukaemia Common?
Burjanivová T.1,2, Madžo J.1,2, Mužíková K.1,2, Meyer C.3, Schneider B.3, Starý J.2, Marschalek R.3, Votava F.4, Trka J.1,2, Zuna J.1,2
CLIP – Childhood Leukaemia Investigation, Prague1 Klinika dětské hematologie a onkologie, 2. LF UK a FN Motol, Praha2 přednosta prof. MUDr. J. Starý, DrSc. Institute of Pharmaceutical Biology/DCAL, University of Frankfurt, Německo3 vedoucí prof. Dr. R. Marschalek Klinika dětí a dorostu, 3. LF UK a FN Královské Vinohrady, Praha4 přednosta prof. MUDr. J. Lebl, CSc. |
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Summary:
While there is enough convincing evidence in childhood acute lymphoblastic leukaemia (ALL),
the data on the pre-natal origin in childhood acute myeloid leukaemia (AML) are less comprehensive.
This study aimed to screen Guthrie cards (neonatal blood spots) of non-infant childhood
AML patients for the presence of their respective leukaemic markers. Guthrie cards of 13 AML
patients (1–14 years) were analysed using PML/RARalpha (n=4), CBFbeta/MYH11 (n=3),
AML1/ETO (n=2), MLL/AF6 (n=1), MLL/AF9 (n=1) and MLL/AF10 (n=1) fusion genes and/or internal
tandem duplication of FLT3 gene (FLT3/ITD) (n=2) as clonotypic markers. Assay sensitivity
determined using serial dilutions of patient DNA into the DNA of a healthy donor allowed to
detect the pre-leukaemic clone in Guthrie card provided 1–3 positive cells were present in the
neonatal blood spot. Patient-specific molecular markers were not found in any patient with AML.
In authors’ previous studies an identical approach was used for patients with ALL and 25% Guthrie
cards were found to be positive. The data suggest that either the prenatal origin of AML is less
frequent or the load of pre-leukaemic cells is significantly lower at birth in AML compared to ALL
cases.
Key words:
prenatal origin, acute myeloid leukaemia, clonal marker
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