TNF-α gene promoter polymorphisms and risk of venous thromboembolism in gastrointestinal cancer patients undergoing chemotherapy

M. Roselli, P. Ferroni, C. Rolfo, M. Peeters, R. Palmirotta, V. Formica, G. Ludovici, A. Laudisi, M. L. De Marchis, F. La Farina, A. Russo, F. Guadagni

Research output: Contribution to journalArticlepeer-review

Abstract

Background: TNF-α has been proposed as a predictive factor for venous thromboembolism (VTE). Genetic polymorphisms could regulate TNF-α production. However, the relationship between TNFA gene variants and VTE is not clarified. This study aims to investigate the predictive role of five different TNFA gene promoter SNPs, or their haplotype combination(s), for a first VTE episode in gastrointestinalcancer out-patients treated with chemotherapy. Patients and methods: Serum TNF-α levels and TNFA -863C/A, -857C/T, -376G/A, -308G/A and -238G/A gene promoter polymorphisms were retrospectively evaluatedin 314 subjects, including 157 controls and 157 Caucasian patients with histologically diagnosed GI cancers beginning chemotherapy delivery (5-fluorouracil either as monotherapy or in combination with platinum compounds or irinotecan). Results: Haplotype analysis showed that a five-loci haplotype (CTGGG haplotype) has higher frequency in GI cancer patients who developed VTE (n = 15) during chemotherapy [odds ratio = 2.7, 95% confidence interval (CI) 1.04-7.11, P = 0.04]. GI patients who remained VTE-free did not differ in CTGGG haplotype frequency from controls. No association was observed between serum TNF-α levels and TNFA haplotype, but both were independent predictors of VTE. Approximately 20% of GI cancer patients carrying the CTGGG haplotype developed VTE compared with 4% of the remaining 101 patients (hazard ratio = 5.6, 95% CI 1.8-17.6, P = 0.003). Conclusion: These results suggest that TNFA might represent a candidate gene contributing to VTE pathogenesis in GI cancer patients and suggest that VTE risk during chemotherapy might be genetically identified. Validation studies are needed for translation into clinical practice.

Original languageEnglish
Pages (from-to)2571-2575
Number of pages5
JournalAnnals of Oncology
Volume24
Issue number10
DOIs
Publication statusPublished - Oct 2013

Keywords

  • Chemotherapy
  • Gastrointestinal cancer
  • Single nucleotide polymorphisms
  • Tumour necrosis factor-a
  • Venous thromboembolism

ASJC Scopus subject areas

  • Oncology
  • Hematology

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