Pyrexia in dabrafenib-treated melanoma patients is not associated with common genetic variation or HLA polymorphisms

Pharmacogenomics. 2016 Apr;17(5):459-62. doi: 10.2217/pgs.16.4. Epub 2016 Mar 29.

Abstract

Aim: Pyrexia is a common adverse event (AE) on dabrafenib treatment (monotherapy or combination with trametinib). Since germline SNPs and HLA alleles are implicated in drug-induced AEs, this study investigated their association with pyrexia.

Patients & methods: 1006 melanoma subjects from five dabrafenib-trametinib clinical studies underwent genotyping for genome-wide SNPs, which enabled imputation of 150 HLA alleles. SNP/HLA allele frequencies were compared between pyrexia cases (n = 218) and controls (n = 361) out of the 1006 subjects by meta-analysis.

Results: This analysis had adequate power to detect association of common SNPs or HLA alleles with moderate to large effects on pyrexia (odds ratio >6), but no significant association was found.

Conclusion: The study suggests that common genetic variation or HLA polymorphisms do not contribute substantially to dabrafenib-induced pyrexia.

Keywords: HLA alleles; SNPs; dabrafenib; pyrexia; trametinib.

Publication types

  • Meta-Analysis

MeSH terms

  • Antineoplastic Agents / adverse effects*
  • Case-Control Studies
  • Fever / chemically induced*
  • Fever / genetics
  • Genetic Association Studies
  • HLA Antigens / genetics*
  • Humans
  • Imidazoles / adverse effects*
  • Melanoma / drug therapy*
  • Melanoma / genetics
  • Oximes / adverse effects*
  • Polymorphism, Single Nucleotide
  • Proto-Oncogene Proteins B-raf / antagonists & inhibitors*
  • Proto-Oncogene Proteins B-raf / genetics

Substances

  • Antineoplastic Agents
  • HLA Antigens
  • Imidazoles
  • Oximes
  • Proto-Oncogene Proteins B-raf
  • dabrafenib