Development of osteonecrosis and improved survival in B-ALL: results of Children’s Oncology Group Trial AALL0232

Osteonecrosis is a significant toxicity of acute lymphoblastic leukemia (ALL) therapy. In retrospective analyses, superior event-free survival was noted among affected adolescents in an earlier trial. We prospectively assessed osteonecrosis incidence, characteristics, and risk factors in patients 1–...

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Veröffentlicht in:Leukemia 2024-02, Vol.38 (2), p.258-265
Hauptverfasser: Mattano, Leonard A., Devidas, Meenakshi, Loh, Mignon L., Raetz, Elizabeth A., Chen, Zhiguo, Winick, Naomi J., Hunger, Stephen P., Carroll, William L., Larsen, Eric C.
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Sprache:eng
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Zusammenfassung:Osteonecrosis is a significant toxicity of acute lymphoblastic leukemia (ALL) therapy. In retrospective analyses, superior event-free survival was noted among affected adolescents in an earlier trial. We prospectively assessed osteonecrosis incidence, characteristics, and risk factors in patients 1–30 years with newly diagnosed high-risk B-ALL on COG AALL0232. Patients were randomized to induction dexamethasone vs prednisone, and interim maintenance high-dose methotrexate vs escalating-dose Capizzi methotrexate/pegaspargase. Event-free and overall survival were compared between patients with/without imaging-confirmed osteonecrosis. Osteonecrosis developed in 322/2730 eligible, evaluable patients. The 5-year cumulative incidence was 12.2%. Risk was greater in patients ≥10 years (hazard ratio [HR], 7.23; P  
ISSN:0887-6924
1476-5551
1476-5551
DOI:10.1038/s41375-023-02099-1