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ETV6::RUNX1 Acute Lymphoblastic Leukemia: how much therapy is needed for cure?
Østergaard, Anna; Fiocco, Marta; de Groot-Kruseman, Hester; Moorman, Anthony V; Vora, Ajay; Zimmermann, Martin; Schrappe, Martin; Biondi, Andrea; Escherich, Gabriele; Stary, Jan; Imai, Chihaya; Imamura, Toshihiko; Heyman, Mats; Schmiegelow, Kjeld; Pieters, Rob.
Affiliation
  • Østergaard A; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Fiocco M; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • de Groot-Kruseman H; Mathematical Institute, Leiden University, Leiden, The Netherlands.
  • Moorman AV; Department of Biomedical Science, Section Medical Statistics, Leiden University Medical Center, Leiden, The Netherlands.
  • Vora A; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Zimmermann M; Dutch Childhood Oncology Group (DCOG), Utrecht, The Netherlands.
  • Schrappe M; Leukaemia Research Cytogenetics Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
  • Biondi A; United Kingdom Acute Lymphoblastic Leukaemia (UKALL) study group, Liverpool, UK.
  • Escherich G; United Kingdom Acute Lymphoblastic Leukaemia (UKALL) study group, Liverpool, UK.
  • Stary J; Department of Haematology, Great Ormond Street Hospital, London, UK.
  • Imai C; Department of Paediatric Haematology and Oncology, Hannover Medical School, 30625, Hannover, Germany.
  • Imamura T; Berlin-Frankfurt-Münster Study Group (BFM), Frankfurt, Germany.
  • Heyman M; Berlin-Frankfurt-Münster Study Group (BFM), Frankfurt, Germany.
  • Schmiegelow K; Department of Paediatrics, University Medical Centre Schleswig-Holstein, Kiel, Germany.
  • Pieters R; Department of Pediatrics, University of Milano-Bicocca, Monza, Italy.
Leukemia ; 38(7): 1477-1487, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38844578
ABSTRACT
Recent trials show 5-year survival rates >95% for ETV6RUNX1 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 ETV6RUNX1 ALL.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Repressor Proteins / Oncogene Proteins, Fusion / Proto-Oncogene Proteins c-ets / Core Binding Factor Alpha 2 Subunit / Precursor Cell Lymphoblastic Leukemia-Lymphoma / ETS Translocation Variant 6 Protein Limits: Humans Language: En Journal: Leukemia Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Repressor Proteins / Oncogene Proteins, Fusion / Proto-Oncogene Proteins c-ets / Core Binding Factor Alpha 2 Subunit / Precursor Cell Lymphoblastic Leukemia-Lymphoma / ETS Translocation Variant 6 Protein Limits: Humans Language: En Journal: Leukemia Year: 2024 Document type: Article