ZAP-70 in chronic lymphocytic leukemia: A meta-analysis
Recent studies have reported that zeta-chain-associated protein kinase 70 (ZAP-70) expression plays a prognostic role in chronic lymphocytic leukemia (CLL). However, these results remain controversial. Thus, we performed a meta-analysis to clarify the prognostic value of ZAP-70 expression in CLL. Re...
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Veröffentlicht in: | Clinica chimica acta 2018-08, Vol.483, p.82-88 |
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Zusammenfassung: | Recent studies have reported that zeta-chain-associated protein kinase 70 (ZAP-70) expression plays a prognostic role in chronic lymphocytic leukemia (CLL). However, these results remain controversial. Thus, we performed a meta-analysis to clarify the prognostic value of ZAP-70 expression in CLL.
Relevant studies were searched in PubMed, Embase, Cochrane library, and Web of Science up to January 2018. Clinicopathological features and prognostic data were extracted from the studies. We pooled estimates and 95% confidence intervals (CIs) and estimated the heterogeneity of studies using Mantel–Haenszel or DerSimonian and Laird method.
Twelve studies that included 1956 patients with CLL were eligible for inclusion. The pooled results revealed that increased ZAP-70 expression was significantly associated with poor overall survival (hazard ratio [HR] = 2.48, 95% CI: 1.72–3.59, P = 0.019, I2 = 53.0%) and event-free survival (HR = 4.17, 95% CI: 2.17–8.01, P = 0.014, I2 = 68.2%) in a random-effects model with significant heterogeneity. Clinicopathological analysis demonstrated that ZAP-70 expression was significantly associated with unmutated immunoglobulin heavy-chain genes, CD38 expression, serum β-2 microglobulin, and lymphocyte doubling time.
Our findings indicated that ZAP-70 was a strong prognostic biomarker for patients with CLL.
•The prognostic role of ZAP-70 in CLL was controversial in previous studies.•Elevated ZAP-70 expression correlated with poor OS and EFS in CLL patients.•ZAP-70 expression was associated with various prognostic factors in CLL•Elevated ZAP-70 expression may be an adverse prognostic biomarker for CLL patients. |
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ISSN: | 0009-8981 1873-3492 |
DOI: | 10.1016/j.cca.2018.04.026 |