Abstract

Background:Tumor lysis syndrome (TLS) is an oncologic emergency commonly seen in children with hemato-lymphoid malignancies. Recombinant urate oxidase (RUO) is used in both the prophylaxis and treatment of TLS. However, in resource-constrained countries, its role is mostly limited to the treatment of established TLS and data regarding the use of RUO and its outcome is sparse. Objective:To describe the outcome of Pediatric TLS following the use of a fixed – dose of RUO. Methods:A retrospective chart review of all children <15 years of age admitted in the Department of Paediatric Oncology, Kidwai Cancer Institute from April 2017 to July 2018 with TLS and treated with a single, fixed – dose (1.5 mg) RUO was undertaken. Results:During the study period, 255 children with hemato-lymphoid malignancies were diagnosed to be at risk of developing TLS. Of these, only 22 (8.6%) children developed TLS and received RUO. Among those with TLS, 15 (68.2%) had Acute Lymphoblastic Leukemia (ALL) while 7 (31.8%) had Non - Hodgkin lymphoma (NHL). 91% (20/22) children had spontaneous TLS and the remainder developed therapy-related TLS. Median age at presentation was 8 years (IQR 5.25,1.75) with 4.5:1 male: female ratio. The mean urate level at admission was 19.12 mg/dl (+/- 8mg/dl) (Range: 10.7–34.5). 91% (20/22) children received RUO at less than 0.15 mg/kg and the median dose of RUO was 0.05 mg/kg (IQR 0.038-0.08). Of the 22 children with TLS, 2 children failed to achieve normal serum urate levels at 24 hours in response to a single fixed-dose of RUO and hence received an extra dose of RUO. Serum urate levels remarkably declined following RUO administration from 19.12 mg/dl (+/-8) to 8.2 mg/dl (+/-3.9), 3.99 mg/dl (+/-1.6) and 2.84 mg/dl (+/-1.3) at 12h, 24h and 48h respectively. AKI was present in 15 (68.2%) children. The median eGFR of the group at diagnosis was 49 ml/min/1.73m2 (IQR 26.3, 70). None of the children required hemodialysis. No significant adverse events occurred. Conclusion:Fixed-dose RUO can achieve rapid, adequate and sustained drop in serum urate levels in Paediatric TLS. It is a useful strategy for managing TLS in resource-constrained settings.

Highlights

  • Tumor lysis syndrome (TLS) is a metabolic oncologic emergency characterised by the triad of hyperuricemia, hyperphosphatemia and hyperkalemia arising due to the abrupt and massive release of intracellular components into systemic circulation following lysis of malignant tumour cells (Coiffier et al, 2008)

  • The present study aims to describe the utility of fixed-dose Recombinant urate oxidase (RUO) in the management of Paediatric TLS in resourceconstrained settings

  • Tumour lysis syndrome can present with diverse clinical features ranging from asymptomatic dyselectrolytemia to life-threatening cardiac arrhythmias, renal failure and seizures (Coiffier et al, 2008)

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Summary

Introduction

Tumor lysis syndrome (TLS) is a metabolic oncologic emergency characterised by the triad of hyperuricemia, hyperphosphatemia and hyperkalemia arising due to the abrupt and massive release of intracellular components into systemic circulation following lysis of malignant tumour cells (Coiffier et al, 2008). The present study aims to describe the utility of fixed-dose RUO in the management of Paediatric TLS in resourceconstrained settings. Methods: A retrospective chart review of all children

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