open access publication

Article, 2024

ETV6::RUNX1 Acute Lymphoblastic Leukemia: how much therapy is needed for cure?

Leukemia, ISSN 0887-6924, Volume 38, 7, Pages 1477-1487, 10.1038/s41375-024-02287-7

Contributors

Ostergaard A. Fiocco M. [1] [2] de Groot-Kruseman H.A. [3] Moorman A.V. 0000-0002-9781-6107 [4] Vora A. 0000-0002-2167-4368 [5] Zimmermann M. [6] Schrappe M. [7] Biondi A. 0000-0002-6757-6173 [8] [9] Escherich G. 0000-0003-2167-3805 [10] [11] Stary J. 0000-0002-6818-7743 [12] Imai C. 0000-0001-7435-3464 [13] Imamura T. 0000-0002-5727-4470 [14] Heyman M. 0000-0001-7637-1949 [15] [16] Schmiegelow K. 0000-0002-0829-4993 [17] Pieters R. 0000-0003-2997-3570 (Corresponding author) [3]

Affiliations

  1. [1] Leiden University
  2. [NORA names: Netherlands; Europe, EU; OECD];
  3. [2] Leiden University Medical Center
  4. [NORA names: Netherlands; Europe, EU; OECD];
  5. [3] Dutch Childhood Oncology Group
  6. [NORA names: Netherlands; Europe, EU; OECD];
  7. [4] Newcastle University
  8. [NORA names: United Kingdom; Europe, Non-EU; OECD];
  9. [5] Great Ormond Street Hospital
  10. [NORA names: United Kingdom; Europe, Non-EU; OECD];

Abstract

Recent trials show 5-year survival rates >95% for ETV6::RUNX1 Acute Lymphoblastic Leukemia (ALL). Since treatment has many side effects, an overview of cumulative drug doses and intensities between eight international trials is presented to characterize therapy needed for cure. A meta-analysis was performed as a comprehensive summary of survival outcomes at 5 and 10 years. For drug dose comparison in non-high risk trial arms, risk group distribution was applied to split the trials into two groups: trial group A with ~70% (range: 63.5–75%) of patients in low risk (LR) (CCLSG ALL2004, CoALL 07-03, NOPHO ALL2008, UKALL2003) and trial group B with ~45% (range: 38.7–52.7%) in LR (AIEOP-BFM ALL 2000, ALL-IC BFM ALL 2002, DCOG ALL10, JACLS ALL-02). Meta-analysis did not show evidence of heterogeneity between studies in trial group A LR and medium risk (MR) despite differences in treatment intensity. Statistical heterogeneity was present in trial group B LR and MR. Trials using higher cumulative dose and intensity of asparaginase and pulses of glucocorticoids and vincristine showed better 5-year event-free survival but similar overall survival. Based on similar outcomes between trials despite differences in therapy intensity, future trials should investigate, to what extent de-escalation is feasible for ETV6::RUNX1 ALL.

Funders

  • Stichting Prinses Máxima Centrum
  • Deutsche Krebshilfe
  • Børnecancerfonden
  • Kræftens Bekæmpelse

Data Provider: Elsevier