Improved Outcome for ALL by Prolonging Therapy for IKZF1 Deletion and Decreasing Therapy for Other Risk Groups

Rob Pieters, Hester de Groot-Kruseman, Marta Fiocco, Femke Verwer, Merian Van Overveld, Edwin Sonneveld, Vincent van der Velden, H Berna Beverloo, Marc Bierings, Natasja Dors, Valérie de Haas, Peter Hoogerbrugge, Inge Van der Sluis, Wim Tissing, Margreet Veening, Judith Boer, Monique Den Boer

Research output: Contribution to journalArticlepeer-review

Abstract

PURPOSE: The ALL10 protocol improved outcomes for children with ALL by stratifying and adapting therapy into three minimal residual disease-defined risk groups: standard risk, medium risk (MR), and high risk. IKZF1-deleted (IKZF1del) ALL in the largest MR group still showed poor outcome, in line with protocols worldwide, accounting for a high number of overall relapses. ALL10 showed high toxicity in Down syndrome (DS) and excellent outcome in ETV6::RUNX1 ALL. Poor prednisone responders (PPRs) were treated as high risk in ALL10. In ALL11, we prolonged therapy for IKZF1del from 2 to 3 years. We reduced therapy for DS by omitting anthracyclines completely, for ETV6::RUNX1 in intensification, and for PPR by treatment as MR.

METHODS: Eight hundred nineteen patients with ALL (age, 1-18 years) were enrolled on ALL11 and stratified as in ALL10. Results were compared with those in ALL10.

RESULTS: The five-year overall survival (OS), event-free survival (EFS), cumulative risk of relapse (CIR), and death in complete remission on ALL11 were 94.2% (SE, 0.9%), 89.0% (1.2), 8.2% (1.1), and 2.3% (0.6), respectively. Prolonged maintenance for IKZF1del MR improved 5-year CIR by 2.2-fold (10.8% v 23.4%; P = .035) and EFS (87.1% v 72.3%; P = .019). Landmark analysis at 2 years from diagnosis showed a 2.9-fold reduction of CIR (25.6%-8.8%; P = .008) and EFS improvement (74.4%-91.2%; P = .007). Reduced therapy did not abrogate 5-year outcome for ETV6::RUNX1 (EFS, 98.3%; OS, 99.4%), DS (EFS, 87.0%; OS, 87.0%), and PPR (EFS, 81.1%; OS, 94.9%).

CONCLUSION: Children with IKZF1del ALL seem to benefit from prolonged maintenance therapy. Chemotherapy was successfully reduced for patients with ETV6::RUNX1, DS, and PPR ALL. It has to be noted that these results were obtained in a nonrandomized study using a historical control group.

Original languageEnglish
Pages (from-to)4130-4142
Number of pages13
JournalJournal of clinical oncology : official journal of the American Society of Clinical Oncology
Volume41
Issue number25
DOIs
Publication statusPublished - 1 Sept 2023

Keywords

  • Child
  • Humans
  • Infant
  • Child, Preschool
  • Adolescent
  • Treatment Outcome
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy
  • Core Binding Factor Alpha 2 Subunit
  • Disease-Free Survival
  • Neoplasm Recurrence, Local/drug therapy
  • Prognosis
  • Antineoplastic Combined Chemotherapy Protocols/adverse effects
  • Ikaros Transcription Factor/genetics

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