Literature DB >> 24141626

Prognostic significance of pretreatment serum cytokines in classical Hodgkin lymphoma.

Preethi Reddy Marri1, Lucy S Hodge, Matthew J Maurer, Steven C Ziesmer, Susan L Slager, Thomas M Habermann, Brian K Link, James R Cerhan, Anne J Novak, Stephen M Ansell.   

Abstract

PURPOSE: Although the International Prognostic Score (IPS) is the gold standard for risk-stratifying patients with classical Hodgkin lymphoma (cHL), these criteria do not accurately predict outcome. As cytokines are critically involved in driving cHL, we tested whether pretreatment serum cytokine levels could provide additional prognostic information. EXPERIMENTAL
DESIGN: Thirty cytokines were measured in pretreatment serum from 140 patients with cHL and compared with 50 nonlymphoma controls. Patients were followed for event-free survival (EFS) and overall survival (OS), and Cox proportional hazards regression models were used to assess the association of individual cytokines and the cytokine profiles with outcome via unadjusted and IPS-adjusted HR.
RESULTS: Twelve cytokines (EGF, bFGF, G-CSF, HGF, IL-6, IL-8, IL-12, IL-2R, IP-10, MIG, TNF-α, and VEGF) were significantly (P < 0.05) higher in patients with cHL than controls; elevated levels of HGF, IL-6, IL-2R, IP-10, and MIG were all associated with poorer EFS. Only interleukin-2 receptor (IL-2R; P = 0.002) and interleukin (IL)-6 (P < 0.001) were independently prognostic. Patients with increased IL-6 and IL-2R had a significantly higher risk of early relapse and death, a finding that remained significant even after IPS-based risk stratification. Although elevated IL-6 and IL-2R correlated with the IPS, soluble CD30 (sCD30), and thymus and activation-related chemokine (TARC) levels, the two-cytokine model remained independently predictive of prognosis.
CONCLUSIONS: Elevated pretreatment serum cytokines are associated with increased disease relapse and inferior survival in cHL. Thus, the pretreatment cytokine profile, particularly serum levels of IL-6 and IL-2R, may be used to identify patients with cHL at high risk for early-disease relapse. ©2013 AACR.

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Year:  2013        PMID: 24141626      PMCID: PMC3867576          DOI: 10.1158/1078-0432.CCR-13-1879

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  23 in total

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2.  Elevated serum levels of CC thymus and activation-related chemokine (TARC) in primary Hodgkin's disease: potential for a prognostic factor.

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3.  Elevated pretreatment interleukin-10 serum level is an International Prognostic Score (IPS)-independent risk factor for early treatment failure in advanced stage Hodgkin lymphoma.

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4.  SIMPLE: a sequential immunoperoxidase labeling and erasing method.

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5.  Soluble IL-2Rα facilitates IL-2-mediated immune responses and predicts reduced survival in follicular B-cell non-Hodgkin lymphoma.

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Journal:  Clin Cancer Res       Date:  2008-11-01       Impact factor: 12.531

7.  Prognostic impact of tumour-infiltrating Th2 and regulatory T cells in classical Hodgkin lymphoma.

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10.  International Prognostic Score in advanced-stage Hodgkin's lymphoma: altered utility in the modern era.

Authors:  Alden A Moccia; Jane Donaldson; Mukesh Chhanabhai; Paul J Hoskins; Richard J Klasa; Kerry J Savage; Tamara N Shenkier; Graham W Slack; Brian Skinnider; Randy D Gascoyne; Joseph M Connors; Laurie H Sehn
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  27 in total

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3.  Prognostic Significance of IL-6 in Hodgkin Lymphoma.

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4.  Comprehensive serum cytokine analysis identifies IL-1RA and soluble IL-2Rα as predictors of event-free survival in T-cell lymphoma.

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6.  Elevated Serum Levels of sCD30 and IL6 and Detectable IL10 Precede Classical Hodgkin Lymphoma Diagnosis.

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7.  Coexistence of Serum Monoclonal Gammopathy of Uncertain Significance and Hodgkin Lymphoma.

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Review 9.  Mechanisms underlying the association between obesity and Hodgkin lymphoma.

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10.  Elevated soluble IL-2Rα, IL-8, and MIP-1β levels are associated with inferior outcome and are independent of MIPI score in patients with mantle cell lymphoma.

Authors:  Mohamad B Sonbol; Matthew J Maurer; Mary J Stenson; Cristine Allmer; Betsy R LaPlant; George J Weiner; William R Macon; James R Cerhan; Thomas E Witzig; Mamta Gupta
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