Macrophages predict treatment outcome in Hodgkin’s lymphoma

Although Hodgkin’s lymphoma (HL) can be considered a successful paradigm of modern treatment strategies, about 15–20% of patients with advanced-stage HL still die following relapse or progressive disease and a similar proportion of patients are over-treated,1,2 leading to treatment-related late sequelae including solid tumors and end-organ dysfunction.3,4 To help guide treatment decisions, the distinction between classical HL and nodular lymphocyte-predominant HL and the separation of limited and advanced-stage disease are widely used in clinical practice. Most patients present with advanced-stage classical HL and for this group of patients the International Prognostic Score was introduced more than a decade ago to improve risk stratification.5 However, neither the International Prognostic Score itself nor any of the individual clinical variables can predict the majority of patients in whom standard therapy will fail to eradicate the disease. Novel biological markers that improve on primary treatment outcome prediction across all clinical stages will, therefore, be critical to advancing the field.

The histological hallmark of HL is the presence of the malignant mononuclear Hodgkin and polynucleated Reed Sternberg (HRS) cells in classical HL and so-called lymphocyte predominant cells in nodular lymphocyte-predominant HL.6 These malignant cells are, however, greatly outnumbered by the reactive cells in the tumor microenvironment.7 Because of the prominent and abnormal immune reaction that creates this variable microenvironment, the biology of HL can be considered unique among lymphomas. Many studies in HL have, therefore, focused on the cellular composition of the microenvironment, not only to gain more insight into the pathobiology of the disease, but also to explore whether these immune-related cells in some way contribute to outcome prediction.

In this issue of the journal, Kamper et al. used immunohistochemistry to investigate a large number (n = 288) of pretreatment biopsies from patients with HL and found a significant correlation between tumor-associated macrophages and adverse treatment outcome. Moreover, they demonstrated a previously unrecognized association of CD68 macrophages with latent Epstein-Barr virus (EBV) infection of the tumor cells.8 This study, together with others listed in Table 1, convincingly validates similar findings of an earlier study suggesting that the number of CD68 macrophages can be used as a reliable biomarker in HL.9

Table 1.Studies on the prognostic value of tumor-associated macrophages in classical Hodgkin’s lymphoma.

Tumor-associated macrophages predict unfavorable treatment outcomes in classical Hodgkin’s lymphoma

Including the study by Kamper et al., multiple reports now support the value of enumerating tumor-associated macrophages in pretreatment biopsies for outcome prediction in classical HL (Table 1). As early as 1985, Ree and Kadin suggested that macrophages in HL biopsies had a prognostic value when they found the number of peanut agglutinin-binding macrophages was correlated with the presence of B symptoms and primary treatment failure.10 However, the authors restricted their analysis to nodular lymphocyte-predominant and mixed cellularity HL. Further evidence of the importance of tumor-associated macrophages was suggested from gene expression profiling studies of larger cohorts of patients, including those with all subtypes of classical HL: these studies identified macrophage signatures as being associated with primary treatment failure.9,11 From these studies, CD68 in particular emerged as the first routinely used immunohistochemical marker detecting a macrophage-associated antigen that was independent from other clinical parameters in multivariate analysis. Of note, the number of CD68 cells in pretreatment biopsies was not only associated with primary treatment failure, but also with failure of subsequent secondary therapies including autologous stem cell transplantation. Thus far, only one published study has found a correlation of gene expression of macrophage-associated genes with favorable outcome.12 However, in two earlier studies, the authors of this study reported that the same genes, namely LYZ and STAT1, were linked to unfavorable outcome, findings that the authors also validated by immunohistochemistry.11,13 Clarification of these contradictory results is needed.

Lack of reproducibility and inconsistency of scoring have been repeatedly named as potential pitfalls for the routine use of immunohistochemical biomarkers. In the present study Kamper et al. address this issue by employing a semi-quantitative computer-assisted stereological analysis system that records the percentage of positively stained cells in an unbiased way that is free of inter- and intra-observer variability. Although it is reassuring that the correlation of tumor-associated macrophages with adverse treatment outcome was validated using this more objective methodology, the standard use of semi-quantitative methods for the assessment of immunohistochemical biomarkers will be confounded by the general lack of availability of such technologies in the routine laboratory setting.

The phenotype of tumor-associated macrophages and correlation with latent Epstein-Barr virus infection

The authors of the present study also used CD163 as a reportedly more specific marker for alternatively activated macrophages (M2) and found similar correlations with overall and event-free survival as for CD68. Interestingly, both CD68 and CD163, determined by immunohistochemistry, were associated with latent EBV infection of the malignant cells as detected by the presence of EBV-encoded RNA. However, when comparing both immunohistochemical stains, the number of CD163 cells seemed to be more closely correlated with EBV infection. These associations have not been previously described and warrant further investigations aiming to define the specific phenotypes of tumor-associated macrophages in HL which are possibly linked to EBV infection. In a re-analysis of our data we were able to confirm a relationship between increased tumor-associated macrophages and EBV positivity; however, virtually all of our cases were of the nodular sclerosis subtype and EBV alone was not associated with treatment outcome (unpublished observations, 2010). EBV infection of HRS cells has been reported in up to 60% of patients and is more frequent in mixed cellularity subtype, although varying with geographical location, age, gender, clinical stage and histological subtype.14 The impact of EBV infection on outcome remains controversial, but appears to be dependent on age. Accordingly, many studies support an association between EBV positivity and adverse outcome in older adult patients,15–17 while in younger and, specifically in pediatric patients, EBV positivity has been linked to better outcome.15,18,19 It will be of interest in subsequent studies to assess the interaction between EBV infection and tumor-associated macrophages as outcome predictors in cHL.

The study in this issue of the journal also raises the question of which marker should be used to reliably and reproducibly identify tumor-associated macrophages and which provides the best information for clinical use. Kamper et al. used two different antibodies against macrophage-associated antigens, namely CD68 and CD163, but no firm conclusions could be reached concerning which marker should be preferred. While CD68 is reported to be a pan-macrophage marker with less specificity, CD163 expression is considered more specific for tumor-infiltrating macrophages.20 However, in their study only CD68 staining retained a significant influence on overall survival in multivariate analysis, rather suggesting that CD68 staining could be used for outcome prediction. Further study is needed to determine the optimal antigen (e.g. CD68 versus CD163), anti-CD68 antibody clone (e.g. KP1 versus PGM1) and scoring thresholds (e.g. manual versus computer-assisted) for detecting HL-associated macrophages.

Combination of CD68 with other biomarkers

The prognostic value of individual biomarkers, especially those based on immunohistochemistry, has been repeatedly demonstrated in lymphoid malignancies. In HL, several biomarkers other than CD68 have been reported to be associated with treatment outcome, in particular markers expressed by certain T-cell subsets.21–24 It, therefore, appears to be a logical next step to explore whether multi-gene predictors combining different markers can exceed the performance of individual biomarkers alone with the aim of better outcome prediction following primary treatment in HL. This approach was already tried in some studies using low-density gene expression techniques12,13 or genome-wide gene-expression profiling, developing predictors for favorable and unfavorable treatment outcome.9 The results show some promise; however, widespread application in routine practice is doubtful given the challenges of technical reproducibility. The preliminary results of an immunohistochemistry study combining two markers, CD68 and FOXP3 (a marker for regulatory T cells), were presented at the ASH 2010 meeting. The authors showed that a combined FOXP3/CD68 immunohistochemistry score was an improvement over the predictive value of the individual markers alone and that this score was applicable to both limited and advanced-stage disease. The value of this combined biomarker strategy must await publication of the complete results of the study.25

Perspective

The number of tumor-associated macrophages has been identified as an adverse prognostic factor in many solid tumors.26 In lymphoid cancers, studies of follicular lymphoma and the most recent data from HL confirm that the presence of macrophages as part of the tumor microenvironment reflects specific tumor biology linked to treatment failure.27 However, many questions remain regarding the exact mechanisms of how HRS cells can attract and induce differentiation of monocytes/macrophages, how macrophages contribute to HRS cell growth and how HRS cells might gain immune privilege through this unique interaction. Besides further detailed molecular characterization of HRS cells, it appears that cellular enrichment and characterization of macrophages from primary clinical material will be critical to gain further insight into the unique phenotype and gene expression profile of HL-associated macrophages. Recently, several molecules that have been implicated in macrophage chemotaxis and signaling have been linked to HL pathobiology, including CSF1R, fractalkine, MIF and CD74.28–30 Some of these molecules might be promising targets for novel drug therapies aiming at macrophages directly or at the interface between HRS cells and their tumor microenvironment.

The research towards the goal of better outcome prediction in HL is dominated by two important questions. First, can information on tumor-associated macrophages and other biomarkers be integrated into routine clinical practice in order to facilitate the decision to escalate or de-escalate primary treatment? Secondly, can the same biomarker profile be used to guide the choice of salvage therapy? To resolve these issues it seems reasonable to combine biomarkers such as CD68 with other immunohistochemical and clinical markers (e.g. regulatory T cells, stage) on the basis of pre-existing data derived from retrospective studies. However, integration of biomarkers into prospective clinical trials is desperately needed to convincingly show an improvement compared to risk stratification based solely on clinical parameters. Finally, future studies should examine whether the approach of identifying biomarkers prior to therapy is equal or superior to assessing disease markers during and after treatment, as realized by interim positron emission tomography scanning31 and measuring serum markers (e.g. TARC).32,33 However, based on ten of the 11 studies listed in Table 1, the prognostic relevance of tumor-associated macrophages in HL has been retrospectively validated and now deserves to be analyzed going forward at both biological and clinical levels in the context of prospective clinical trials.

Acknowledgments

This work is supported by a postdoctoral fellowship of the Cancer Research Society (CRS, Steven E. Drabin Fellowship), by the Michael Smith Foundation for Health Research (MSFHR), and the Lymphoma Research Foundation (LRF) to CS. RDG is supported by the Canadian Institutes for Health Research (CIHR #178536).

Footnotes

• Dr. Christian Steidl is a research fellow in the Department of Pathology and Centre for Lymphoid Cancer of the British Columbia Cancer Agency. He has a keen interest in the biology of lymphoid malignancies with a focus on interactions of neoplastic B cells with the microenvironment. Dr. Pedro Farinha worked as a fellow with Dr. Gascoyne in Vancouver and now practises pathology and does translational research at Centro Hospitalar Lisboa Central in Lisbon, Portugal. Dr. Randy Gascoyne is a hematopathologist and scientist at the BC Cancer Agency with a focus on lymphoid cancers.
• Related Original Article on page 269
• Financial and other disclosures provided by the author using the ICMJE (www.icmje.org) Uniform Format for Disclosure of Competing Interests are available with the full text of this paper at www.haematologica.org.