| Literature DB >> 18577710 |
Laura Z Rassenti1, Sonia Jain, Michael J Keating, William G Wierda, Michael R Grever, John C Byrd, Neil E Kay, Jennifer R Brown, John G Gribben, Donna S Neuberg, Feng He, Andrew W Greaves, Kanti R Rai, Thomas J Kipps.
Abstract
Leukemia-cell expression of ZAP-70, CD38, or unmutated immunoglobulin heavy chain variable region genes (U-IGHV) each is associated with aggressive disease in patients with chronic lymphocytic leukemia (CLL). To assess the relative strength of each marker, we defined thresholds for designating a case as positive for CD38 or ZAP-70 in a test cohort of 307 patients and used these data-defined criteria to stratify patients in an independent cohort of 705 patients. Multivariable analysis revealed that ZAP-70 was the strongest risk factor. Knowledge of the IGHV mutation status or CD38 did not improve our ability to predict the time to first treatment except for ZAP-70-negative cases, which could be segregated into 2 groups of intermediate-risk or low-risk disease based on whether they expressed unmutated or mutated IGHV. ZAP-70 maintained its high relative prognostic value for the subset of patients with early-stage, asymptomatic disease, including patients evaluated within 1 year of diagnosis. Although it is premature to recommend therapy based on these risk factors, patients with ZAP-70-positive CLL cells should be monitored closely for disease progression as they have a median time from diagnosis to requiring initial therapy by standard criteria of approximately 3 years.Entities:
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Year: 2008 PMID: 18577710 PMCID: PMC2518894 DOI: 10.1182/blood-2007-05-092882
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113