Germline variants in the CYP19A1 gene are related to specific adverse events in aromatase inhibitor users: a substudy of Dutch patients in the TEAM trial

• Published in: Breast cancer research and treatment 2014-04, Vol.144 (3), p.599-606
• Main Authors: Fontein, Duveken B. Y., Houtsma, Daniel, Nortier, Johan W. R., Baak-Pablo, Renee F., Kranenbarg, Elma Meershoek-Klein, van der Straaten, Tahar R. J. H. M., Putter, Hein, Seynaeve, Caroline, Gelderblom, Hans, van de Velde, Cornelis J. H., Guchelaar, Henk-Jan
• Format: Article
• Language: English
• Subjects: Adult; Aged; Aged, 80 and over; Analysis; Aromatase - genetics; Aromatase Inhibitors - administration & dosage; Aromatase Inhibitors - adverse effects; Breast cancer; Breast Neoplasms - drug therapy; Breast Neoplasms - genetics; Breast Neoplasms - pathology; Cancer research; Cancer therapies; Care and treatment; Chemotherapy; Clinical Trial; Combined Modality Therapy; Complications and side effects; Cytochrome P-450; Female; Genes; Genetic research; Genotype; Germ-Line Mutation; Humans; Inhibitor drugs; Medicine; Medicine & Public Health; Middle Aged; Neoplasm Grading; Neoplasm Staging; Netherlands; Odds Ratio; Oncology; Pharmacology; Polymorphism, Single Nucleotide; Postmenopausal women; Postmenopause; Risk Factors; Side effects; Single nucleotide polymorphisms; Tamoxifen; Treatment Outcome
• ISSN: 0167-6806; 1573-7217
• DOI: 10.1007/s10549-014-2873-2

Musculoskeletal adverse events (MSAEs) and vasomotor symptoms (VMSs) are known side-effects of aromatase inhibitors, and may be related to genetic variations of the aromatase gene (CYP19A1). We investigated the relationship between these specific AEs and single nucleotide polymorphisms (SNPs) in the CYP19A1 gene in postmenopausal, hormone receptor-positive early breast cancer (BC) patients treated with adjuvant exemestane for 5 years. Dutch patients who were randomized to receive 5 years of exemestane in the Tamoxifen Exemestane Adjuvant Multinational (TEAM) trial were included. A tagging-SNP approach was performed, covering 80 % of variations of the CYP19A1 gene with 30 SNPs. Logistic regression analyses were used to assess the risk of reporting VMSs or MSAEs in relation to genotypes within selected SNPs. Of 737 included patients, 281 patients reported at least one MSAE ( n  = 210) or VMS ( n  = 163). Homozygous AA genotype of rs934635 was associated with a significantly higher odds of MSAEs (multivariate odds ratio (OR) 4.66, p  = 0.008) and VMSs (multivariate OR 2.78, p  = 0.044). Regarding both rs1694189 and rs7176005, the homozygous variant genotypes (TT) were associated with a higher odds of VMSs, but not MSAEs (OR 1.758, p  = 0.025 and OR 6.361, p  = 0.021, respectively). Our exploratory analysis demonstrated that some CYP19A1 gene variations may be associated with MSAEs and/or VMSs. Specifically, patients with the homozygous variant rs934635 genotype reported more MSAEs and VMSs. Although further confirmatory studies are warranted, genomic profiling can help identify patients at an increased risk of reporting these specific AEs, potentiating further personalized BC treatment.