Tumor-associated macrophages predict inferior outcomes in classic Hodgkin lymphoma: a correlative study from the E2496 Intergroup trial

Author:

Tan King L.1,Scott David W.1,Hong Fangxin2,Kahl Brad S.3,Fisher Richard I.4,Bartlett Nancy L.5,Advani Ranjana H.6,Buckstein Rena7,Rimsza Lisa M.8,Connors Joseph M.1,Steidl Christian1,Gordon Leo I.9,Horning Sandra J.10,Gascoyne Randy D.1

Affiliation:

1. Centre for Lymphoid Cancer, British Columbia Cancer Agency and the University of British Columbia, Vancouver, BC;

2. Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA;

3. Department of Medicine-Hematology/Oncology, University of Wisconsin, Madison, WI;

4. James P. Wilmot Cancer Center, University of Rochester, Rochester, NY;

5. Washington University School of Medicine, St Louis, MO;

6. School of Medicine, Stanford University, Stanford, CA;

7. Odette Cancer Center, Sunnybrook Hospital, Toronto, ON;

8. Department of Pathology, University of Arizona, Tucson, AZ;

9. Division of Hematology/Oncology and the Robert H. Lurie Comprehensive Cancer Centre, Northwestern University Feinberg School of Medicine, Chicago, IL; and

10. Genentech Inc, South San Francisco, CA

Abstract

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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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