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FCGR3A/2A polymorphisms and diffuse large B-cell lymphoma outcome treated with immunochemotherapy: a meta-analysis on 1134 patients from two prospective cohorts.
Ghesquières, Hervé; Larrabee, Beth R; Haioun, Corinne; Link, Brian K; Verney, Aurélie; Slager, Susan L; Ketterer, Nicolas; Ansell, Stephen M; Delarue, Richard; Maurer, Matthew J; Fitoussi, Olivier; Habermann, Thomas M; Peyrade, Fréderic; Dogan, Ahmet; Molina, Thierry J; Novak, Anne J; Tilly, Hervé; Cerhan, James R; Salles, Gilles.
Afiliación
  • Ghesquières H; Department of Hematology, Centre Hospitalier Lyon Sud, Pierre-Bénite, France.
  • Larrabee BR; Centre de Recherche en Cancérologie de Lyon - INSERM U 1052/CNRS UMR 5286/Centre Léon Bérard, Lyon, France.
  • Haioun C; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
  • Link BK; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
  • Verney A; Lymphoid Malignancies Unit, Hôpital Henri Mondor, Assistance Publique-Hôpitaux de Paris (AP-HP) and University Paris Est, Créteil, France.
  • Slager SL; Holden Comprehensive Cancer Center, University of Iowa, Iowa City, IA, USA.
  • Ketterer N; Centre de Recherche en Cancérologie de Lyon - INSERM U 1052/CNRS UMR 5286/Centre Léon Bérard, Lyon, France.
  • Ansell SM; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
  • Delarue R; Department of Oncology, University Hospital, Lausanne, Switzerland.
  • Maurer MJ; Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA.
  • Fitoussi O; Department of Hematology, Necker Hospital, Paris, France.
  • Habermann TM; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
  • Peyrade F; Onco-Hematology, Polyclinique Bordeaux-Nord, Bordeaux, France.
  • Dogan A; Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA.
  • Molina TJ; Medical Oncology, Centre Antoine Lacassagne, Nice, France.
  • Novak AJ; Departments of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Tilly H; Department of Pathology, Necker Hospital, Paris, France.
  • Cerhan JR; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
  • Salles G; Department of Hematology, Centre Henri Becquerel, Rouen, France.
Hematol Oncol ; 35(4): 447-455, 2017 Dec.
Article en En | MEDLINE | ID: mdl-27282998
ABSTRACT
Single nucleotide polymorphisms (SNPs) in FCγ-receptor genes FCGR3A (rs396991) and FCGR2A (rs1801274) influence the affinity of the Fc portion of anti-CD20 immunoglobulin G1 monoclonal antibody. Their roles in diffuse large B-cell lymphoma (DLBCL) treated with rituximab in combination with anthracycline-based chemotherapy remain controversial. To address this question, we genotyped FCGR2A and FCGR3A SNPs in two prospective DLBCL cohorts from Lymphoma Study Association trials (N = 554) and Iowa/Mayo Specialized Program Of Research Excellence (N = 580). Correlations with treatment response and hematological toxicity were assessed in Lymphoma Study Association. Correlation with event-free survival (EFS) and overall survival (OS) was performed in both cohorts, followed by a meta-analysis to increase power. Our study shows the absence of correlation between these SNPs and treatment response. Grades 3 and 4 febrile neutropenia during treatment was more frequently observed in FCGR3A VV (39%) than VF (29%) and FF (32%) carriers (p = 0.04). Our analysis for EFS and OS shows that FCGR3A was not associated with outcome. In a meta-analysis using an ordinal model, FCGR2A (per R allele) was associated with a better EFS (hazard ratio = 0.87; 95%CI, 0.76-0.99; p = 0.04) and OS (hazard ratio = 0.86; 95%CI, 0.73-1.00; p = 0.05) which was not altered after adjustment for the International Prognostic Index. Overall, our data demonstrate that patients with DLBCL with the low-affinity FCγRIIA RR had an unexpectedly better outcome than FCγRIIA H carriers. Whether rituximab efficacy is improved in FCγRIIA RR patients due a clearance reduction or other functions of FCγRIIA in DLBCL should be investigated (clinicaltrials.gov identifiers NCT00135499, NTC00135499 NCT00140595, NCT00144807, NCT00144755, NCT01087424, and NCT00301821). Copyright © 2016 John Wiley & Sons, Ltd.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfoma de Células B Grandes Difuso / Receptores de IgG / Inmunoterapia Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male Idioma: En Revista: Hematol Oncol Año: 2017 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfoma de Células B Grandes Difuso / Receptores de IgG / Inmunoterapia Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male Idioma: En Revista: Hematol Oncol Año: 2017 Tipo del documento: Article País de afiliación: Francia