TY - JOUR
T1 - Therapy with low-dose azacitidine for MDS in children and young adults: A retrospective analysis of the EWOG-MDS study group
AU - Cseh, Annamaria M.
AU - Niemeyer, Charlotte M.
AU - Yoshimi, Ayami
AU - Catala, Albert
AU - Frühwald, Michael C.
AU - Hasle, Henrik
AU - van den Heuvel-Eibrink, Mary M.
AU - Lauten, Melchior
AU - De Moerloose, Barbara
AU - Smith, Owen P.
AU - Bernig, Toralf
AU - Gruhn, Bernd
AU - Kulozik, Andreas E.
AU - Metzler, Markus
AU - Olcay, Lale
AU - Suttorp, Meinolf
AU - Furlan, Ingrid
AU - Strahm, Brigitte
AU - Flotho, Christian
N1 - Publisher Copyright:
© 2016 John Wiley & Sons Ltd.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Low-dose azacitidine is efficient and safe in the therapy of malignant myeloid disorders in adults but data in children are lacking. We present a retrospective analysis of 24 children and young adults with myelodysplastic syndrome (MDS) who received azacitidine at the time of first diagnosis or relapse after allotransplant (2 children were treated with azacitidine both initially and for relapse). Diagnoses were refractory cytopenia of childhood (N = 4), advanced primary MDS (N = 9) and secondary MDS (N = 11). The median duration of treatment was four cycles. Azacitidine was well tolerated, but cytopenias led to dose reduction in five cases. Treatment was discontinued in one child because of impaired renal function. Sixteen MDS patients were treated with azacitidine at first diagnosis. One complete clinical remission was observed and one child showed complete marrow remission; six children experienced stable disease with haematological improvement. Ten children received azacitidine for relapsed MDS after transplant: of these, seven experienced stable disease for 2-30 cycles (median 3), including one patient with haematological improvement for seven cycles. In summary, azacitidine is effective in some children with MDS and appears to be a non-toxic option in palliative situations to prolong survival.
AB - Low-dose azacitidine is efficient and safe in the therapy of malignant myeloid disorders in adults but data in children are lacking. We present a retrospective analysis of 24 children and young adults with myelodysplastic syndrome (MDS) who received azacitidine at the time of first diagnosis or relapse after allotransplant (2 children were treated with azacitidine both initially and for relapse). Diagnoses were refractory cytopenia of childhood (N = 4), advanced primary MDS (N = 9) and secondary MDS (N = 11). The median duration of treatment was four cycles. Azacitidine was well tolerated, but cytopenias led to dose reduction in five cases. Treatment was discontinued in one child because of impaired renal function. Sixteen MDS patients were treated with azacitidine at first diagnosis. One complete clinical remission was observed and one child showed complete marrow remission; six children experienced stable disease with haematological improvement. Ten children received azacitidine for relapsed MDS after transplant: of these, seven experienced stable disease for 2-30 cycles (median 3), including one patient with haematological improvement for seven cycles. In summary, azacitidine is effective in some children with MDS and appears to be a non-toxic option in palliative situations to prolong survival.
UR - http://www.scopus.com/inward/record.url?scp=84960090251&partnerID=8YFLogxK
U2 - 10.1111/bjh.13915
DO - 10.1111/bjh.13915
M3 - Journal articles
C2 - 26766110
AN - SCOPUS:84960090251
SN - 0007-1048
VL - 172
SP - 930
EP - 936
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 6
ER -