Childhood acute lymphoblastic leukemia: Four years evaluation of protocols 2013 and 2016 in a single center in Indonesia, a lower-middle-income country

  • Sutaryo Sutaryo
  • , Pudjo Hagung Widjajanto
  • , Sri Mulatsih
  • , Bambang Ardianto
  • , Alexandra Widita Swipratami Pangarso
  • , Eddy Supriyadi
  • , Ignatius Purwanto
  • , Claudia Priska Adelin
  • , Rahmadani Puji Lestari
  • , Lintang Sagoro
  • , Scholastika Dita Christian
  • , Dea Sella Sabrina
  • , Natasha Verena
  • , Wijnanda Adriana Kors
  • , Gertjan J.L. Kaspers
  • , Anjo J.P. Veerman

Research output: Contribution to journalArticlepeer-review

10 Citations (Scopus)

Abstract

Background: The prognosis of childhood acute lymphoblastic leukemia (ALL) in Indonesia, a lower-middle-income country (LMIC), is lower than in high income countries (HICs). The Indonesian ALL2013 protocol resulted in too many toxic deaths (21%) and abandonments (11%). Therefore, we drafted an adapted protocol, ALL2016. Main changes: no anthracyclines in standard risk (SR), prednisone replaced dexamethasone at induction in high risk (HR), and anthracyclines and cyclophosphamide were rescheduled in HR. Procedure: Patients (aged: 1–18 years) were stratified into SR and HR. HR was defined as age over 10 years, leucocyte count over 50 × 109/L, central nervous system (CNS) involvement, mediastinal mass, T-cell phenotype, testicular involvement, or poor prednisone response. Results: ALL2013 included 174 patients (106 SR and 68 HR) and ALL2016 188 (91 SR and 97 HR). Although the number of HR patients was significantly higher in ALL2016 (51.6% vs. 39.1%; p =.017), the outcome of ALL2016 improved over ALL2013 (4-year-probable overall survival (pOS) 60.1% vs. 50.0%; p =.042 and 4-year-probable event-free survival (pEFS) 49.5% vs. 36.8%; p =.018). ALL2016 showed a nonsignificant advantage for SR patients (4-year-pEFS 56.0% vs. 47.2%; p =.220 and 4-year-pOS 70.3% vs. 61.3%; p =.166), but less toxic deaths (7% vs. 20%; p =.011). In HR group, the outcomes were significantly better in ALL2016 (4-year-pEFS 43.3% vs. 20.6%; p =.004; 4-year-pOS 50.5% vs. 32.4%; p =.014) especially due to less relapses (31% vs. 62%; p =.001). Isolated CNS relapses went down from 18 to 8% in HR (p =.010) and 11 to 5% in SR (p =.474). Both SR and HR showed lower numbers of abandonment in ALL2016 (6% vs. 14%; p =.039). Conclusions: Overall ALL2016 results improved over ALL2013. Modest changes in protocol resulted in less initial toxicity and abandonments.

Original languageEnglish
Article numbere29875
Pages (from-to)e29875
JournalPediatric Blood and Cancer
Volume69
Issue number11
DOIs
Publication statusPublished - Nov 2022

Keywords

  • acute lymphoblastic leukemia
  • lower-middle-income country
  • protocol development
  • survival
  • Cyclophosphamide/therapeutic use
  • Prednisone/therapeutic use
  • Recurrence
  • Prognosis
  • Humans
  • Indonesia/epidemiology
  • Treatment Outcome
  • Antineoplastic Combined Chemotherapy Protocols/therapeutic use
  • Disease-Free Survival
  • Dexamethasone/therapeutic use
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy

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