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Lack of association of tumor-associated macrophages with clinical outcome in patients with classical Hodgkin's lymphoma. Ann Oncol 2012 Mar;23(3):736-742

Date

05/24/2011

Pubmed ID

21602260

Pubmed Central ID

PMC3331732

DOI

10.1093/annonc/mdr157

Scopus ID

2-s2.0-84857534118 (requires institutional sign-in at Scopus site)   85 Citations

Abstract

BACKGROUND: A recent study demonstrated that an increased number of CD68+ macrophages were correlated with primary treatment failure, shortened progression-free survival (PFS) and disease-specific survival (DSS) in patients with classical Hodgkin's lymphoma (cHL).

PATIENTS AND METHODS: The aim of the present study was to verify the relationship between the number of CD68+ and CD163+ macrophages with clinical outcomes in a cohort of 265 well-characterized patients with cHL treated uniformly with the standard doxorubicin, bleomycin, vinblastine and dacarbazine chemotherapy regimen. Two pairs of hematopathologists carried out independent pathological evaluations of tissue microarray slides.

RESULTS: There were no associations between clinical characteristics and the expression of CD68 or CD163. However, higher levels of CD68 and CD163 expression were correlated with the presence of Epstein-Barr virus-positive Hodgkin tumor cells (P = 0.01 and 0.037, respectively). The expression of CD68 or CD163 was not associated with either the PFS or the DSS.

CONCLUSION: CD68 and CD163 expression require further evaluation before their use can be recommended for prognostic stratification of patients with cHL.

Author List

Azambuja D, Natkunam Y, Biasoli I, Lossos IS, Anderson MW, Morais JC, Spector N

Author

Matthew W. Anderson MD, PhD Assistant Professor in the Pathology department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Adolescent
Adult
Aged
Aged, 80 and over
Antigens, CD
Antigens, Differentiation, Myelomonocytic
Antineoplastic Combined Chemotherapy Protocols
Disease-Free Survival
Epstein-Barr Virus Infections
Female
Hodgkin Disease
Humans
Immunohistochemistry
In Situ Hybridization
Kaplan-Meier Estimate
Macrophages
Male
Middle Aged
Prognosis
Receptors, Cell Surface
Tissue Array Analysis
Treatment Outcome
Young Adult