| Literature DB >> 22948049 |
King L Tan1, David W Scott, Fangxin Hong, Brad S Kahl, Richard I Fisher, Nancy L Bartlett, Ranjana H Advani, Rena Buckstein, Lisa M Rimsza, Joseph M Connors, Christian Steidl, Leo I Gordon, Sandra J Horning, Randy D Gascoyne.
Abstract
Increased tumor-associated macrophages (TAMs) are reported to be associated with poor prognosis in classic Hodgkin lymphoma (CHL). We investigated the prognostic significance of TAMs in the E2496 Intergroup trial, a multicenter phase 3 randomized controlled trial comparing ABVD and Stanford V chemotherapy in locally extensive and advanced stage CHL. Tissue microarrays were constructed from formalin-fixed, paraffin-embedded tumor tissue and included 287 patients. Patients were randomly assigned into training (n = 143) and validation (n = 144) cohorts. Immunohistochemistry for CD68 and CD163, and in situ hybridization for EBV-encoded RNA were performed. CD68 and CD163 IHC were analyzed by computer image analysis; optimum thresholds for overall survival (OS) were determined in the training cohort and tested in the independent validation cohort. Increased CD68 and CD163 expression was significantly associated with inferior failure-free survival and OS in the validation cohort. Increased CD68 and CD163 expression was associated with increased age, EBV-encoded RNA positivity, and mixed cellularity subtype of CHL. Multivariate analysis in the validation cohort showed increased CD68 or CD163 expression to be significant independent predictors of inferior failure-free survival and OS. We demonstrate the prognostic significance of TAMs in locally extensive and advanced-stage CHL in a multicenter phase 3 randomized controlled clinical trial.Entities:
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Year: 2012 PMID: 22948049 PMCID: PMC3476539 DOI: 10.1182/blood-2012-04-421057
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113