Your browser doesn't support javascript.
loading
Angiogenesis' related genetic variants alter clinical features and prognosis of diffuse large B-cell lymphoma patients.
Brito, Angelo Borsarelli Carvalho; Delamain, Marcia Torresan; Fanelli, Marcello Ferreti; Soares, Fernando Augusto; de Souza, Cármino Antônio; Vassallo, José; Lima, Carmen Silvia Passos.
Affiliation
  • Brito ABC; Department of Internal Medicine, Faculty of Medical Sciences, University of Campinas, Campinas, São Paulo, Brazil.
  • Delamain MT; Haematology and Haemotherapy Centre, University of Campinas, Campinas, São Paulo, Brazil.
  • Fanelli MF; A. C. Camargo Cancer Centre, São Paulo, São Paulo, Brazil.
  • Soares FA; A. C. Camargo Cancer Centre, São Paulo, São Paulo, Brazil.
  • de Souza CA; Department of Internal Medicine, Faculty of Medical Sciences, University of Campinas, Campinas, São Paulo, Brazil.
  • Vassallo J; Haematology and Haemotherapy Centre, University of Campinas, Campinas, São Paulo, Brazil.
  • Lima CSP; A. C. Camargo Cancer Centre, São Paulo, São Paulo, Brazil.
Tumour Biol ; 43(1): 129-140, 2021.
Article in En | MEDLINE | ID: mdl-34219681
OBJECTIVES: Single nucleotide variants (SNVs) in vascular endothelial growth factor A (VEGFA) and VEGFA receptor (KDR) genes confer different inherited abilities in angiogenesis (AG) pathway. We aimed in the present study to evaluate influence of six VEGFA and four KDR SNVs in clinical features and survival of diffuse large B-cell lymphoma (DLBCL) patients. METHODS: One hundred and sixty-eight DLBCL patients diagnosed between June 2009-September 2014 were enrolled in the study. Patients were homogeneously treated with R-CHOP. Genotypes were identified in genomic DNA by real-time polymerase chain reaction. RESULTS: Patients with VEGFA -634CC and +936CT or TT genotypes were at increased risk of showing grade III / IV toxicities and not achieving complete remission with treatment, and shorter event-free and overall survival were seen in patients with VEGFA -1154GA or AA genotype and VEGFA ATAGCC haplotype. CONCLUSION: Our data suggest that inherited abnormalities in AG's gene modulate clinical features and prognosis of DLBCL patients homogeneously treated with R-CHOP.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Biomarkers, Tumor / Lymphoma, Large B-Cell, Diffuse / Polymorphism, Single Nucleotide / Vascular Endothelial Growth Factor A / Neovascularization, Pathologic Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Tumour Biol Journal subject: NEOPLASIAS Year: 2021 Document type: Article Affiliation country: Brazil Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Biomarkers, Tumor / Lymphoma, Large B-Cell, Diffuse / Polymorphism, Single Nucleotide / Vascular Endothelial Growth Factor A / Neovascularization, Pathologic Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Tumour Biol Journal subject: NEOPLASIAS Year: 2021 Document type: Article Affiliation country: Brazil Country of publication: Netherlands