Haematologica (Oct 2011)

Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial

  • Rachel Wade,
  • Maria Chiara Di Bernardo,
  • Sue Richards,
  • Davide Rossi,
  • Dalemari Crowther-Swanepoel,
  • Gianluca Gaidano,
  • David G. Oscier,
  • Daniel Catovsky,
  • Richard S. Houlston

DOI
https://doi.org/10.3324/haematol.2011.043471
Journal volume & issue
Vol. 96, no. 10

Abstract

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Background There is variability in the outcome of patients with chronic lymphocytic leukemia with apparently the same stage of disease. Identifying genetic variants that influence patients’ outcome and response to treatment may provide important insights into the biology of the disease.Design and Methods We investigated the possibility that genetic variation influences outcome by conducting a genome-wide analysis of 346,831 single nucleotide polymorphisms in 356 patients entered into a phase III trial comparing the efficacy of fludarabine, chlorambucil, and fludarabine with cyclophosphamide as first-line treatment. Genotypes were linked to individual patients’ outcome data and response to chemotherapy. The association between genotype and progression-free survival was assessed by Cox regression analysis adjusting for treatment and clinicopathology.Results The strongest associations were shown for rs1949733 (ACOX3; P=8.22x10-7), rs1342899 (P=7.72x10−7) and rs11158493 (PPP2R5E; P=8.50×10−7). In addition, the 52 single nucleotide polymorphisms associated at P