Ig V Gene Mutation Status and CD38 Expression As Novel Prognostic Indicators in Chronic Lymphocytic Leukemia

Rajendra N. Damle(North Shore University Hospital), Tarun Wasil(North Shore University Hospital), Franco Fais(North Shore University Hospital), Fabio Ghiotto(North Shore University Hospital), Angelo Valetto(North Shore University Hospital), Steven L. Allen(North Shore University Hospital), Aby Buchbinder(North Shore University Hospital), Daniel R. Budman(North Shore University Hospital), Klaus Dittmar(North Shore University Hospital), Jonathan E. Kolitz(North Shore University Hospital), Stuart M. Lichtman(North Shore University Hospital), Philip Schulman(North Shore University Hospital), Vincent Vinciguerra(North Shore University Hospital), Kanti R. Rai(North Shore University Hospital), Manlio Ferrarini(North Shore University Hospital), Nicholas Chiorazzi(North Shore University Hospital)
Blood
September 15, 1999
Cited by 2,589

Abstract

Cellular immunophenotypic studies were performed on a cohort of randomly selected IgM(+) B-chronic lymphocytic leukemia (B-CLL) cases for which Ig V(H) and V(L) gene sequences were available. The cases were categorized based on V gene mutation status and CD38 expression and analyzed for treatment history and survival. The B-CLL cases could be divided into 2 groups. Those patients with unmutated V genes displayed higher percentages of CD38(+) B-CLL cells (>/=30%) than those with mutated V genes that had lower percentages of CD38(+) cells (<30%). Patients in both the unmutated and the >/=30% CD38(+) groups responded poorly to continuous multiregimen chemotherapy (including fludarabine) and had shorter survival. In contrast, the mutated and the <30% CD38(+) groups required minimal or no chemotherapy and had prolonged survival. These observations were true also for those patients who stratified to the Rai intermediate risk category. In the mutated and the <30% CD38(+) groups, males and females were virtually equally distributed, whereas in the unmutated and the >/=30% CD38(+) groups, a marked male predominance was found. Thus, Ig V gene mutation status and the percentages of CD38(+) B-CLL cells appear to be accurate predictors of clinical outcome in B-CLL patients. These parameters, especially CD38 expression that can be analyzed conveniently in most clinical laboratories, should be valuable adjuncts to the present staging systems for predicting the clinical course in individual B-CLL cases. Future evaluations of new therapeutic strategies and drugs should take into account the different natural histories of patients categorized in these manners.


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