The pharmacogenomics journal · 2016
Sunitinib-induced hypertension in CYP3A4 rs4646437 A-allele carriers with metastatic renal cell carcinoma.
СтатьяМногоцентровое исследованиеНаблюдательное исследованиеНазвание и аннотация: Перевод в очереди
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Diekstra M H, Belaustegui A, Swen J J, Boven E, Castellano D, Gelderblom H, Mathijssen R H, García-Donas J, Rodríguez-Antona C, Rini B I, Guchelaar H-J
Аннотация
The single nucleotide polymorphism (SNP) rs4646437G>A in CYP3A4 was suggested to be related to sunitinib toxicity. Our objective was to perform an in-depth investigation of the association between this SNP and sunitinib toxicity and efficacy using a large cohort of metastatic renal cell carcinoma (mRCC) patients. We collected DNA and clinical information of mRCC patients treated with sunitinib. SNP rs4646437 in CYP3A4 was tested for associations with toxicity using logistic regression. Cox regression modeling was used for association analysis of rs4646437 with progression-free survival (PFS) and overall survival (OS). In a total of 287 patients, the A-allele of CYP3A4 rs4646437 was associated with an increased risk for hypertension (odds ratio=2.4, 95% confidence interval: 1.1-5.2, P=0.021) and showed no significant association with PFS or OS. In conclusion, hypertension is more likely to occur in A-allele carriers of the CYP3A4 rs4646437 variant in our cohort of mRCC patients treated with sunitinib.
Предметные рубрики MeSH
AdultAgedAged, 80 and overAngiogenesis InhibitorsCarcinoma, Renal CellChi-Square DistributionCytochrome P-450 CYP3ADisease-Free SurvivalEuropeFemaleGene FrequencyGenetic Predisposition to DiseaseHeterozygoteHomozygoteHumansHypertensionIndolesKidney NeoplasmsLogistic ModelsMaleMiddle AgedMultivariate AnalysisOdds RatioOhioPharmacogenomic VariantsPhenotypePolymorphism, Single NucleotideProportional Hazards ModelsProtein Kinase InhibitorsPyrrolesRetrospective StudiesRisk FactorsSunitinibTime FactorsTreatment Outcome