Literature DB >> 24592992

High intratumoral macrophage content is an adverse prognostic feature in anaplastic large cell lymphoma.

Martin B Pedersen1, Allan V Danielsen, Stephen J Hamilton-Dutoit, Knud Bendix, Peter Nørgaard, Michael B Møller, Torben Steiniche, Francesco d'Amore.   

Abstract

AIMS: Macrophage infiltration has been associated with prognosis in several cancers, including lymphoma, but has not been assessed systematically in anaplastic large cell lymphoma (ALCL). The aim of the study was to correlate expression of the macrophage-associated antigens CD68 and CD163 with pre-therapeutic parameters and outcome in a cohort of treatment-naive ALCL patients. METHODS AND
RESULTS: Pre-therapeutic tumour specimens from 52 patients with ALCL were included in a tissue microarray. The intratumoral macrophage content was assessed by immunohistochemical staining for CD68 and CD163, and quantified using digital image analysis. Anaplastic lymphoma kinase (ALK)-positive patients were significantly younger and had a favourable outcome compared with ALK-negative ALCL patients (median age: 42 versus 59 years; P = 0.008). However, ALK expression was not a significant predictor when adjusting for age. Although classical risk factors were distributed evenly between the compared groups, high intratumoral content of CD68 and/or CD163 correlated with poor outcome, in both univariate and multivariate analyses. High intratumoral CD163 content showed the strongest adverse association with both overall and progression-free survival in ALK-negative patients (P < 0.001).
CONCLUSIONS: A high content of intratumoral CD68- and/or CD163-positive macrophages correlates with an adverse outcome in ALK-negative ALCL.
© 2014 John Wiley & Sons Ltd.

Entities:  

Keywords:  CD163; CD68; anaplastic large cell lymphoma; immunohistochemistry; macrophages; prognosis

Mesh:

Substances:

Year:  2014        PMID: 24592992     DOI: 10.1111/his.12407

Source DB:  PubMed          Journal:  Histopathology        ISSN: 0309-0167            Impact factor:   5.087


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