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Erschienen in: Journal of Cancer Research and Clinical Oncology 10/2015

01.10.2015 | Original Article – Clinical Oncology

Prognostic value of CD56 in patients with acute myeloid leukemia: a meta-analysis

verfasst von: Shuangnian Xu, Xi Li, Jianmin Zhang, Jieping Chen

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 10/2015

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Abstract

Purpose

Extensive studies have investigated the prognostic value of CD56 for patients with acute myeloid leukemia (AML), but the results remained inconclusive. The aim of this meta-analysis is to resolve this controversial issue.

Methods

A systematic search of PubMed, Embase, Cochrane Library, and CBM was performed to identify studies that assessed the prognostic value of CD56 in AML patients. Pooled hazard ratios (HRs) with 95 % confidence intervals (CIs) for overall survival (OS) and disease-free survival (DFS) and pooled odds ratio (OR) with 95 % CIs for complete remission rate (CRR) and relapse rate (RR) were calculated.

Results

Totally, 32 studies with 4074 patients were included. For AML with t(8;21) translocation, CD56 overexpression was associated with shorter OS (HR 2.22; 95 % CI 1.30–3.78) and DFS (HR 2.63; 95 % CI 1.10–6.29) and increased RR (OR 3.29; 95 % CI 1.67–6.48), but did not affect CRR (OR 0.94; 95 % CI 0.49–1.80). For AML with t(15;17) translocation, CD56 overexpression was associated with shorter OS (HR 2.43; 95 % CI 1.66–3.57) and DFS (HR 4.27; 95 % CI 1.15–15.78), increased RR (OR 3.11; 95 % CI 2.01–4.81), and decreased CRR (OR 0.42; 95 % CI 0.25–0.72). For AML as a whole, CD56 overexpression was associated with shorter OS (HR 1.74; 95 % CI 1.38–2.19) and DFS (HR 2.38; 95 % CI 1.87–3.02), increased RR (OR 5.19; 95 % CI 2.84–9.48), and decreased CRR (OR 0.62; 95 % CI 0.41–0.96).

Conclusions

This meta-analysis indicated that CD56 overexpression may be an adverse prognostic factor for AML.
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Metadaten
Titel
Prognostic value of CD56 in patients with acute myeloid leukemia: a meta-analysis
verfasst von
Shuangnian Xu
Xi Li
Jianmin Zhang
Jieping Chen
Publikationsdatum
01.10.2015
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 10/2015
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-015-1977-3

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