| Literature DB >> 32552472 |
Robert J Hayashi1, Stuart S Winter2, Kimberly P Dunsmore3, Meenakshi Devidas4, Zhiguo Chen5, Brent L Wood6, Michelle L Hermiston7, David T Teachey8, Sherrie L Perkins9, Rodney R Miles9, Elizabeth A Raetz10, Mignon L Loh7, Naomi J Winick11, William L Carroll10, Stephen P Hunger8, Megan S Lim12, Thomas G Gross13, Catherine M Bollard14.
Abstract
PURPOSE: The Children's Oncology Group (COG) protocol AALL0434 evaluated the safety and efficacy of multi-agent chemotherapy with Capizzi-based methotrexate/pegaspargase (C-MTX) in patients with newly diagnosed pediatric T-cell lymphoblastic lymphoma (T-LL) and gained preliminary data using nelarabine in high-risk patients. PATIENTS AND METHODS: The trial enrolled 299 patients, age 1-31 years. High-risk (HR) patients had ≥ 1% minimal detectable disease (MDD) in the bone marrow at diagnosis or received prior steroid treatment. Induction failure was defined as failure to achieve a partial response (PR) by the end of the 4-week induction. All patients received the augmented Berlin-Frankfurt-Muenster (ABFM) C-MTX regimen. HR patients were randomly assigned to receive or not receive 6 5-day courses of nelarabine incorporated into ABFM. Patients with induction failure were nonrandomly assigned to ABFM C-MTX plus nelarabine. No patients received prophylactic cranial radiation; however, patients with CNS3 disease (CSF WBC ≥ 5/μL with blasts or cranial nerve palsies, brain/eye involvement, or hypothalamic syndrome) were ineligible.Entities:
Year: 2020 PMID: 32552472 PMCID: PMC7479761 DOI: 10.1200/JCO.20.00531
Source DB: PubMed Journal: J Clin Oncol ISSN: 0732-183X Impact factor: 44.544