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The prognostic significance of early treatment response in pediatric relapsed acute myeloid leukemia: results of the international study Relapsed AML 2001/01

U. Creutzig, M. Zimmermann, MN. Dworzak, B. Gibson, R. Tamminga, J. Abrahamsson, SY. Ha, H. Hasle, A. Maschan, Y. Bertrand, G. Leverger, C. von Neuhoff, B. Razzouk, C. Rizzari, P. Smisek, OP. Smith, B. Stark, D. Reinhardt, GL. Kaspers,

. 2014 ; 99 (9) : 1472-8.

Jazyk angličtina Země Itálie

Typ dokumentu časopisecké články, multicentrická studie, randomizované kontrolované studie

Perzistentní odkaz   https://www.medvik.cz/link/bmc15023459

The prognostic significance of early response to treatment has not been reported in relapsed pediatric acute myeloid leukemia. In order to identify an early and easily applicable prognostic factor allowing subsequent treatment modifications, we assessed leukemic blast counts in the bone marrow by morphology on days 15 and 28 after first reinduction in 338 patients of the international Relapsed-AML2001/01 trial. Both day 15 and day 28 status was classified as good (≤20% leukemic blasts) in 77% of patients. The correlation between day 15 and 28 blast percentages was significant, but not strong (Spearman correlation coefficient = 0.49, P<0.001). Survival probability decreased in a stepwise fashion along with rising blast counts at day 28. Patients with bone marrow blast counts at this time-point of ≤5%, 6-10%, 11-20% and >20% had 4-year probabilities of survival of 52%±3% versus 36%±10% versus 21%±9% versus 14%±4%, respectively, P<0.0001; this trend was not seen for day 15 results. Multivariate analysis showed that early treatment response at day 28 had the strongest prognostic significance, superseding even time to relapse (< or ≥12 months). In conclusion, an early response to treatment, measured on day 28, is a strong and independent prognostic factor potentially useful for treatment stratification in pediatric relapsed acute myeloid leukemia. This study was registered with ISRCTN code: 94206677.

AIEOP c o Department of Pediatrics Hospital S Gerardo Monza Italy

BFM AML Group Hannover c o Pediatric Hematology Oncology Hannover Medical High School Germany

BFM AML Group St Anna Children's Hospital and Children's Cancer Research Institute Department of Pediatrics Medical University of Vienna Austria

c o Department of Haematology and Oncology Our Lady's Children's Hospital Dublin Ireland

c o Unité d'Onco Hématologie Pédiatrique Hôpital d'Enfants Armand Trousseau Paris France

Center of Pediatric Hematology Oncology Schneider Children's Medical Center of Israel Petah Tikva Israel

CPH c o Department of Pediatric Hematology and Oncology 2nd Faculty of Medicine and University Hospital Motol Charles University Prague Czech Republic

Department of Pediatrics Aarhus University Hospital Skejby Denmark

FRALLE CLCG

FRALLE CLCG c o Institut d'Hématologie et d'Oncologie Pédiatrique Lyon France

Hong Kong Paediatric Haematology and Oncology Study Group c o Department of Paediatrics and Adolescent Medicine Queen Mary Hospital Hong Kong China

NOPHO

NOPHO Department of Pediatrics Queen Silvia's Children's Hospital Göteborg Sweden

Pediatric Oncology Hematology Beatrix Children's Hospital UMCG Groningen The Netherlands Dutch Childhood Oncology Group The Hague The Netherlands

Pediatric Oncology Hematology VU University Medical Center Amsterdam The Netherlands Dutch Childhood Oncology Group The Hague The Netherlands

Research Center for Pediatric Hematology Oncology and Immunology Moscow Russia

St Jude's Children Research Hospital Memphis TN USA c o Children's Center For Cancer and Blood Diseases Peyton Manning Children's Hospital at St Vincent Indianapolis IN USA

UK CCLG

UK NCRI Childhood Leukaemia Group Department of Paediatric Haematology Royal Hospital for Sick Children Glasgow Scotland UK

Citace poskytuje Crossref.org

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