| Literature DB >> 24428673 |
David A Rizzieri1, Jeffrey L Johnson, John C Byrd, Gerard Lozanski, Kristie A Blum, Bayard L Powell, Thomas C Shea, Sreenivasa Nattam, Eva Hoke, Bruce D Cheson, Richard A Larson.
Abstract
To improve long-term outcomes for Burkitt leukaemia/lymphoma (BL) or aggressive lymphomas in adults, we assessed the benefit of adding rituximab and filgrastim support to a dose-dense modified chemotherapy regimen from the Cancer and Leukemia Group B (CALGB) 9251 trial. One hundred and five patients (aged 19-79 years) were enrolled; 27% were >60 years old; 47% had high or high-intermediate risk by International Prognostic Index (IPI) criteria. Common severe toxicities included stomatitis/upper gastrointestinal toxicity (69%), renal insufficiency (10%), neurological events (25%) and pulmonary events (18%). Seven died from treatment-related causes (one central nervous system bleed, four infections, two respiratory failure); five were >60 years old. Results in this adult population are encouraging as complete response (CR) was observed in 83% and 4-year event-free (EFS) and overall survivals (OS) were 74% and 78%, respectively. Results compare favourably to our prior chemotherapy alone study (CALGB 9251) but despite this, high-risk patients still had worse outcomes. In conclusion, short duration, intensive chemo-immunotherapy is feasible and should be considered in adults with BL as it results in high remission rates and durable remissions.Entities:
Keywords: Burkitt leukaemia; Burkitt lymphoma; chemo-immunotherapy; rituximab
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Year: 2014 PMID: 24428673 PMCID: PMC3996561 DOI: 10.1111/bjh.12736
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998