Infectious Agents and Cancer

unofficial impact factor 2.33

This article is part of the supplement: Proceedings of the 11th International Conference on Malignancies in AIDS and Other Acquired Immunodeficiencies (ICMAOI): Basic, Epidemiologic, and Clinical Research

Open Access Poster presentation

Immunophenotypic analysis of AIDS-related diffuse large B-cell lymphoma and clinical implications in patients from AIDS malignancies consortium clinical trials 010 and 034

A Chadburn1*, A Chiu1, Y Lee2, X Chen1, E Hyjek1, A Banhmam3, A Noy4, A Kaplan5, J Sparano6, K Bhatia7, E Cesarman1 and the Aids Malignancy Consortium

  • * Corresponding author: A Chadburn

Author Affiliations

1 Weill Cornell Medical College, New York, New York, USA

2 University of Alabama at Birmingham, Birmingham, Alabama, USA

3 Nuffield Department of Clinical Laboratory Sciences, University of Oxford, Headington, Oxford, UK

4 Memorial Sloan Kettering Cancer Center, New York, New York, USA

5 University of California-San Francisco, San Francisco, California, USA

6 Albert Einstein Comprehensive Cancer Center, New York, New York, USA

7 National Cancer Institute, National Institutes of Health Washington, D.C., USA

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Infectious Agents and Cancer 2009, 4(Suppl 2):P14 doi:10.1186/1750-9378-4-S2-P14

Published: 17 June 2009

First paragraph (this article has no abstract)

Diffuse large B cell lymphoma represents a clinically heterogeneous disease, and several immunohistochemical strategies have been shown to help prognosticate clinical outcome. These include subdivision into germinal center (GC) and non-germinal center (non-GC) subtypes, proliferation index (measured by expression of Ki67), and expression of BCL-2, FOXP1 or Blimp-1/PRDM1. We sought to determine whether immunohistochemical analyses of biopsies from DLBCL patients with HIV infection are similarly relevant for prognostication.