PMID- 30915498 OWN - NLM STAT- MEDLINE DCOM- 20190605 LR - 20191210 IS - 1432-0584 (Electronic) IS - 0939-5555 (Linking) VI - 98 IP - 6 DP - 2019 Jun TI - Survival and risk factors for mortality in pediatric patients with acute myeloid leukemia in a single reference center in low-middle-income country. PG - 1403-1411 LID - 10.1007/s00277-019-03661-7 [doi] AB - Despite advances in therapy and care for children with acute myeloid leukemia (AML), survival rates for children in low- and middle-income countries (LMICs) remain poor. We studied risk factors for mortality and survival in children with AML in a LMIC to develop strategies to improve survival for AML children in these countries. This retrospective cohort (2000-2014) analyzed newly diagnosed AML patients (age < 19 years) at a reference center in Brazil. Demographic and clinical variables were reviewed by AML subtype: acute promyelocytic leukemia (APL), AML with Down syndrome (AML-DS), and other AML subtypes. Cumulative hazard risk for early death (ED) until 6 weeks of treatment and risk factors for mortality were determined by the multivariate Cox hazard models. Survival was assessed for each AML subtypes. A total of 220 patients were diagnosed: APL 50 (22.7%), AML-DS 16 (7.3%), and other AML subtypes 154 (70.0%). The cumulative hazard function values for ED for all patients with AML were 12.5% (95% CI 8.5-18.4%); for each AML patients subtypes: APL, 21.7% (95% CI 11.7-40.5%); AML-DS, 6.2% (95% CI 0.9-44.4%); and other AML subtypes, 10.2% (95% CI 6.2-17.0%). White blood cell count (cutoff 10 x 10(9)/L for APL and 100 x 10(9)/L for other AML subtypes) and Afro-descendance were significant risk factors for mortality in APL and other AML subtypes, respectively. Overall survival for patients with APL, AML-DS, and other AML subtypes was 66.8%, 62.5%, and 38.0%, respectively. APL patients had the highest incidence of ED and those with other subtypes had increased relapse risk. We also observed high rates of death in complete remission mainly due to infection. Better risk classification and identification of risk factors for infection may improve the survival of these patients. FAU - Lins, Mecneide Mendes AU - Lins MM AD - Pediatric Oncology Unit, Instituto de Medicina Integral Prof. Fernando Figueira, Recife, PE, Brazil. FAU - Mello, Maria Julia Goncalves AU - Mello MJG AUID- ORCID: 0000-0003-4645-8343 AD - Pediatric Research Center, Instituto de Medicina Integral Prof. Fernando Figueira, Rua dos Coelhos, 300 Boa Vista, Recife, PE, 50070-550, Brazil. mjuliagmello@gmail.com. FAU - Ribeiro, Raul C AU - Ribeiro RC AD - Department of Oncology and Global Pediatric Medicine, St. Jude Children's Research Hospital, Memphis, TN, USA. AD - Department of Pediatrics, University of Tennessee Health Science Center, Memphis, TN, USA. FAU - De Camargo, Beatriz AU - De Camargo B AD - Research Center, Instituto Nacional de Cancer, Rio de Janeiro, Brazil. FAU - de Fatima Pessoa Militao de Albuquerque, Maria AU - de Fatima Pessoa Militao de Albuquerque M AD - Departamento de Saude Coletiva (Collective Health Department) of CPqAM, FIOCRUZ, Recife, Brazil. FAU - Thuler, Luiz Claudio Santos AU - Thuler LCS AD - Research Center, Instituto Nacional de Cancer, Rio de Janeiro, Brazil. LA - eng PT - Journal Article DEP - 20190326 PL - Germany TA - Ann Hematol JT - Annals of hematology JID - 9107334 SB - IM MH - Adolescent MH - Antineoplastic Combined Chemotherapy Protocols/therapeutic use MH - Brazil/epidemiology MH - Child MH - Child, Preschool MH - Comorbidity MH - Developing Countries MH - Down Syndrome/epidemiology MH - Female MH - Humans MH - Income MH - Infant MH - Infections/mortality MH - Leukemia, Myeloid, Acute/drug therapy/economics/ethnology/*mortality MH - Leukemia, Promyelocytic, Acute/drug therapy/mortality MH - Male MH - Proportional Hazards Models MH - Recurrence MH - Retrospective Studies MH - Risk Factors OTO - NOTNLM OT - AML OT - Acute promyelocytic leukemia OT - Children OT - Low- and middle-income countries OT - Risk factor OT - Survival EDAT- 2019/03/28 06:00 MHDA- 2019/06/06 06:00 CRDT- 2019/03/28 06:00 PHST- 2018/10/31 00:00 [received] PHST- 2019/03/06 00:00 [accepted] PHST- 2019/03/28 06:00 [pubmed] PHST- 2019/06/06 06:00 [medline] PHST- 2019/03/28 06:00 [entrez] AID - 10.1007/s00277-019-03661-7 [pii] AID - 10.1007/s00277-019-03661-7 [doi] PST - ppublish SO - Ann Hematol. 2019 Jun;98(6):1403-1411. doi: 10.1007/s00277-019-03661-7. Epub 2019 Mar 26.