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Prognostic significance of FCGR2B expression for the response of DLBCL patients to rituximab or obinutuzumab treatment
M. Nowicka, LK. Hilton, M. Ashton-Key, CE. Hargreaves, C. Lee, R. Foxall, MJ. Carter, SA. Beers, KN. Potter, CR. Bolen, C. Klein, A. Knapp, F. Mir, M. Rose-Zerilli, C. Burton, W. Klapper, DW. Scott, LH. Sehn, U. Vitolo, M. Martelli, M. Trneny,...
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
C34999/A18087
Cancer Research UK - United Kingdom
ECMC C24563/A15581
Cancer Research UK - United Kingdom
NLK
Directory of Open Access Journals
od 2016
PubMed Central
od 2016
Europe PubMed Central
od 2016
ROAD: Directory of Open Access Scholarly Resources
od 2016
- MeSH
- cyklofosfamid terapeutické užití MeSH
- difúzní velkobuněčný B-lymfom * farmakoterapie genetika MeSH
- humanizované monoklonální protilátky MeSH
- lidé MeSH
- prognóza MeSH
- protokoly protinádorové kombinované chemoterapie * terapeutické užití MeSH
- receptory IgG genetika MeSH
- rituximab terapeutické užití MeSH
- vinkristin terapeutické užití MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Fc γ receptor IIB (FcγRIIB) is an inhibitory molecule capable of reducing antibody immunotherapy efficacy. We hypothesized its expression could confer resistance in patients with diffuse large B-cell lymphoma (DLBCL) treated with anti-CD20 monoclonal antibody (mAb) chemoimmunotherapy, with outcomes varying depending on mAb (rituximab [R]/obinutuzumab [G]) because of different mechanisms of action. We evaluated correlates between FCGR2B messenger RNA and/or FcγRIIB protein expression and outcomes in 3 de novo DLBCL discovery cohorts treated with R plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) reported by Arthur, Schmitz, and Reddy, and R-CHOP/G-CHOP-treated patients in the GOYA trial (NCT01287741). In the discovery cohorts, higher FCGR2B expression was associated with significantly shorter progression-free survival (PFS; Arthur: hazard ratio [HR], 1.09; 95% confidence interval [CI], 1.01-1.19; P = .0360; Schmitz: HR, 1.13; 95% CI, 1.02-1.26; P = .0243). Similar results were observed in GOYA with R-CHOP (HR, 1.26; 95% CI, 1.00-1.58; P = .0455), but not G-CHOP (HR, 0.91; 95% CI, 0.69-1.20; P = .50). A nonsignificant trend that high FCGR2B expression favored G-CHOP over R-CHOP was observed (HR, 0.67; 95% CI, 0.44-1.02; P = .0622); however, low FCGR2B expression favored R-CHOP (HR, 1.58; 95% CI, 1.00-2.50; P = .0503). In Arthur and GOYA, FCGR2B expression was associated with tumor FcγRIIB expression; correlating with shorter PFS for R-CHOP (HR, 2.17; 95% CI, 1.04-4.50; P = .0378), but not G-CHOP (HR, 1.37; 95% CI, 0.66-2.87; P = .3997). This effect was independent of established prognostic biomarkers. High FcγRIIB/FCGR2B expression has prognostic value in R-treated patients with DLBCL and may confer differential responsiveness to R-CHOP/G-CHOP.
1st Medical Faculty Charles University Prague Czech Republic
BC Cancer Centre for Lymphoid Cancer Vancouver BC Canada
Canada's Michael Smith Genome Sciences Centre Vancouver BC Canada
Department of Hematopathology University of Schleswig Holstein Campus Kiel Kiel Germany
Department of Medicine University of British Columbia Vancouver BC Canada
Department of Molecular Biology and Biochemistry Simon Fraser University Burnaby BC Canada
Department of Translational and Precision Medicine Hematology Sapienza University Rome Italy
F Hoffmann La Roche Ltd Basel Switzerland
Genentech Inc South San Francisco CA
Multidisciplinary Oncology Outpatient Clinic Candiolo Cancer Institute FPO IRCCS Candiolo Italy
Roche Innovation Center Zurich Schlieren Switzerland
Royal Marsden Hospital Sutton United Kingdom
School of Cancer Sciences University of Southampton Southampton United Kingdom
Southampton University Hospitals NHS Foundation Trust Southampton United Kingdom
Citace poskytuje Crossref.org
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