PMID- 34054042 OWN - NLM STAT- MEDLINE DCOM- 20220215 LR - 20231002 IS - 1536-3678 (Electronic) IS - 1077-4114 (Linking) VI - 44 IP - 1 DP - 2022 Jan 1 TI - Management of Hyperleukocytosis in Childhood Acute Leukemia Without Leukapheresis and Rasburicase Prophylaxis. PG - 12-18 LID - 10.1097/MPH.0000000000002225 [doi] AB - Indications of leukapheresis (LPh) and the prophylactic use of rasburicase in tumor lysis syndrome (TLS) of patients with acute leukemia with hyperleukocytosis are not clear. In this retrospective single-center pediatric study, the outcomes of patients with hyperleukocytosis were reviewed. There were 48 patients with acute lymphoblastic leukemia (ALL) and 13 patients with acute myeloblastic leukemia (AML). The treatment strategies included hyperhydration, allopurinol administration, strict monitoring, and early initiation of induction chemotherapy (CT). No patient underwent LPh because it was not available. Rasburicase was used only in 3 ALL patients with hyperuricemia when the drug was available. Laboratory and clinical TLS developed in 54.16% and 14.58% of patients with ALL, respectively. Laboratory and clinical TLS developed in 76.92% and 15.38% of patients with AML, respectively. No patient developed grade III to V TLS requiring dialysis. Thirteen patients (21.3%) had pulmonary leukostasis on admission, but recovered with CT and nasal oxygen. During the first 14 days of presentation, cerebral leukostasis/coagulopathy-related early death (ED) was 4.2% and 7.7% in patients with ALL and AML, respectively, and all of these patients had a white blood cell count >/=400,000/microL. There was also 1 infection-related death. Patients with hyperleukocytosis can be treated without LPh and liberal use of rasburicase. Renal failure is no longer a cause of ED. Intracranial hemorrhage is the main cause of ED, especially in patients already presenting with this complication. LPh may be performed in patients with leukostasis, if it is not possible to start induction CT early. When resources are limited, rasburicase should be administered in patients presenting with or developing hyperuricemia and/or renal dysfunction. CI - Copyright (c) 2021 Wolters Kluwer Health, Inc. All rights reserved. FAU - Aylan Gelen, Sema AU - Aylan Gelen S AD - Department of Pediatrics, Division of Pediatric Hematology, Kocaeli University, Kocaeli, Turkey. FAU - Sarper, Nazan AU - Sarper N FAU - Zengin, Emine AU - Zengin E FAU - Azizoglu, Mehmet AU - Azizoglu M LA - eng PT - Journal Article PL - United States TA - J Pediatr Hematol Oncol JT - Journal of pediatric hematology/oncology JID - 9505928 RN - 08GY9K1EUO (rasburicase) RN - EC 1.7.3.3 (Urate Oxidase) SB - IM MH - Adolescent MH - Child MH - Child, Preschool MH - Female MH - Humans MH - *Induction Chemotherapy MH - Infant MH - Infant, Newborn MH - Leukapheresis MH - Leukemia, Myeloid, Acute/*drug therapy MH - Leukocytosis/etiology/*prevention & control MH - Male MH - Precursor Cell Lymphoblastic Leukemia-Lymphoma/*drug therapy MH - Retrospective Studies MH - Urate Oxidase/*administration & dosage COIS- The authors declare no conflict of interest. EDAT- 2021/06/01 06:00 MHDA- 2022/02/16 06:00 CRDT- 2021/05/31 05:57 PHST- 2020/07/27 00:00 [received] PHST- 2021/05/04 00:00 [accepted] PHST- 2021/06/01 06:00 [pubmed] PHST- 2022/02/16 06:00 [medline] PHST- 2021/05/31 05:57 [entrez] AID - 00043426-202201000-00002 [pii] AID - 10.1097/MPH.0000000000002225 [doi] PST - ppublish SO - J Pediatr Hematol Oncol. 2022 Jan 1;44(1):12-18. doi: 10.1097/MPH.0000000000002225.