Protocol AML-MM-2000 treatment results of unfavorable prognostic group in children with acute myeloid leukemia
- Authors: Kirsanova N.P.1, Aleinikova O.V.1, Kustanovich A.M.1, Savitskay T.V.1, Yutskevich R.I.1, Volochnik E.V.1, Baidun L.V.2, Mareiko Y.E.1, Strongin Y.S.1, Minakovskay N.V.1, Migal N.V.1, Proleskovskay I.V.1, Emelyanova I.V.1, Karas O.V.1, Drekov A.G.1, Maschan M.M.3,2, Litvinov D.V.3,2, Myakova N.V.3,2, Skorobogatova E.V.3,2, Baidildina D.D.2, Kalinina I.I.2, Solopova G.G.2, Suntsova E.V.2, Petrova U.N.2, Hachatryan L.A.2, Scheider M.M.3, Maschan A.A.3
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Affiliations:
- Republic Centre for Paediatric Oncology and Haematology
- Russian Children Clinical Hospital
- Federal Research Center of Pediatric Hematology, Oncology and Immunology
- Issue: No 1 (2009)
- Pages: 5-13
- Section: HEMATOLOGIC MALIGNANCIES: TREATMENT, SUPPORTIVE CARE
- Published: 24.02.2009
- URL: https://oncohematology.abvpress.ru/ongm/article/view/645
- DOI: https://doi.org/10.17650/1818-8346-2009-0-1-5-13
- ID: 645
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Abstract
Protocol AML-MM-2000 treatment results of unfavorable prognostic group in children with primary acute myeloid leukemia (AML) in Russia and Belarus are presented. 105 children at the age from 2 weeks till 18 years (a median age — 10.8 years) are included in the study. In 91 patients (86.7%) hematological remission have reached, from them 34 patients (37.4%) are in the first continuous complete remission (CCR). 6-years overall survival (OS), event-free survival (EFS) and relapse-free survival (RFS) rate for all group of patients was 0.35 ±} 0.05; 0.32 ±} 0.04 and 0.43 ±} 0.05, respectively. Survival analysis of children with different cytogenetic anomalies has allowed to define two prognostic groups of patients: the intermediate prognosis, including patients with normal kariotype and t(9;11) which EFS and RFS rate was 40—50%, and unfavorable prognosis with EFS and RFS rate less than 40%. The efficiency analysis of three postremission therapy type (allogeneic and autological hematopoietic stem cells transplantation (HSCT) and chemotherapy (HT)) in intermediate and unfavorable prognostis groups was carried out. High efficiency of related HLA-identical HSCT in patients both intermediate and unfavorable prognostis groups have been shown. Autological HSCT is possible in intermediate prognosis patients with absence of HLA-identical siblings and in unfavorable prognosis patients with absence of HLA-identical unrelated donor.
About the authors
N. P. Kirsanova
Republic Centre for Paediatric Oncology and Haematology
Author for correspondence.
Minsk
BelarusO. V. Aleinikova
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusA. M. Kustanovich
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusT. V. Savitskay
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusR. I. Yutskevich
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusE. V. Volochnik
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusL. V. Baidun
Russian Children Clinical HospitalRussian Federation
Yu. E. Mareiko
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusYu. S. Strongin
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusN. V. Minakovskay
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusN. V. Migal
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusI. V. Proleskovskay
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusI. V. Emelyanova
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusO. V. Karas
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusA. G. Drekov
Republic Centre for Paediatric Oncology and Haematology
Minsk
BelarusM. M. Maschan
Federal Research Center of Pediatric Hematology, Oncology and Immunology; Russian Children Clinical HospitalRussian Federation
D. V. Litvinov
Federal Research Center of Pediatric Hematology, Oncology and Immunology; Russian Children Clinical HospitalRussian Federation
N. V. Myakova
Federal Research Center of Pediatric Hematology, Oncology and Immunology; Russian Children Clinical HospitalRussian Federation
E. V. Skorobogatova
Federal Research Center of Pediatric Hematology, Oncology and Immunology; Russian Children Clinical HospitalRussian Federation
D. D. Baidildina
Russian Children Clinical HospitalRussian Federation
I. I. Kalinina
Russian Children Clinical HospitalRussian Federation
G. G. Solopova
Russian Children Clinical HospitalRussian Federation
E. V. Suntsova
Russian Children Clinical HospitalRussian Federation
U. N. Petrova
Russian Children Clinical HospitalRussian Federation
L. A. Hachatryan
Russian Children Clinical HospitalRussian Federation
M. M. Scheider
Federal Research Center of Pediatric Hematology, Oncology and ImmunologyRussian Federation
A. A. Maschan
Federal Research Center of Pediatric Hematology, Oncology and ImmunologyRussian Federation
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