ZAP-70 expression and prognosis in chronic lymphocytic leukaemia.

Orchard, J. A., Ibbotson, R. E., Davis, Z. A., Wiestner, A., Rosenwald, A., Thomas, P., Hamblin, T. J.H., Staudt, L. M. and Oscier, D. G., 2004. ZAP-70 expression and prognosis in chronic lymphocytic leukaemia. Lancet, 363 (9403), pp. 105-111.

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DOI: 10.1016/S0140-6736(03)15260-9

Abstract

Background Chronic lymphocytic leukaemia (CLL) is a heterogeneous disease; many patients never need treatment, whereas some have poor outcomes. New treatments, which can induce complete remissions, allow patients with poor outlook to be treated while they are still asymptomatic. Whether or not the IgVH gene is mutated is the best predictor of clinical outcome, but this assay is unsuited to the routine laboratory. The gene coding for ZAP- 70, a tyrosine kinase protein normally expressed in T and NK cells, has been shown by gene-expression profiling to be differentially expressed between patients with mutated and unmutated IgVH genes. We assessed whether ZAP-70 could be used as a prognostic marker in CLL. Methods We developed a flow cytometry assay for ZAP-70 protein expression and investigated its concordance with ZAP-70 mRNA expression, IgVH gene mutational status, and clinical outcome in 167 patients with CLL. Findings We showed high concordance between ZAP-70 protein expression and IgVH gene mutations. 108 patients (65%) had mutated IgVH genes and were ZAP-70 negative; 46 (28%) had unmutated IgVH genes and were ZAP-70 positive. Findings were discordant in 13 patients: six (4%) had mutated IgVH genes but were ZAP-70 positive, and seven (4%) had unmutated IgVH genes and were ZAP-70 negative. Expression of mRNA showed 97% concordance with ZAP-70 protein. Median survival was 24·4 years (95% CI 15·1–33·8) in ZAP-70 negative patients and 9·3 years (7·0–11·5) in those who were ZAP-70 positive (hazard ratio 5·5, 2·8–10·8). Interpretation ZAP-70 protein, which can be measured by flow cytometry in the general laboratory, is a reliable prognostic marker in CLL, equivalent to that of IgVH gene mutational.

Item Type:Article
ISSN:0140-6736
Subjects:Technology > Medicine and Health
Group:School of Health and Social Care > Centre for Social Work and Social Policy
ID Code:1189
Deposited By:INVALID USER
Deposited On:03 Apr 2007
Last Modified:07 Mar 2013 14:36

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