Abstract

IntroductionThe prevalence of 2R/2R TYMS genotype is variable but estimated to be around 20–30% in Caucasians. The clinical relevance of TYMS 2R/2R genotype in predicting severe fluoropyrimidine-related adverse events (FrAE) is controversial. Here, we explored the prevalence and clinical relevance of 2R/2R TYMS genotype.MethodsBetween 2011 and 2018, 126 patients were genotyped for TYMS. FrAEs were graded according to CTCAE version 5.0. Fisher’s exact test was used for statistical analysis.ResultsThe prevalence of TYMS 2R/2R genotype was 24.6%. Among patients with TYMS genotypes (N = 71) that predict decreased TS expression, 2R/2R TYMS genotype was the most common TYMS genotype seen in female (57%) and African American (60%) patients. Among patients with genotypes that predict increased TS expression (N = 55), 12 patients had grade 3–4 FrAEs (22%), while among patients with genotypes that predict decreased TS expression (N = 71), 30 patients had grade 3–4 FrAEs (42%) (p = 0.0219). Compared to patients with genotypes predicting increased TS expression, 17 out of 31 patients (55%) with TYMS 2R/2R genotype had grade 3–4 FrAEs (p = 0.0039) and 15 out 40 patients (38%) with TYMS 2R/3RC and TYMS 3RC/3RC genotype had grade 3–4 FrAEs (p = 0.1108).ConclusionThe prevalence of TYMS 2R/2R genotype was 24.6%, and it had a unique sex and ethnic distribution. Polymorphism in the promoter region of TYMS gene that predicts decreased TS expression due to 2R/2R variant was associated with grade 3–4 FrAEs. These data suggest that genotyping patients who are not DPD deficient for TYMS might identify patients at risk of severe FrAEs.

Highlights

  • Introduction The prevalence of2R/2R thymidylate synthase gene (TYMS) genotype is variable but estimated to be around 20–30% in Caucasians

  • Between 2011 and 2018, a total of 126 patients with GI malignancies were genotyped for TYMS and had no identifiable high-risk DPYD variants

  • Among patients with TYMS genotypes that predict decreased thymidylate synthase (TS) expression, 2R/ 2R TYMS genotype was the most common TYMS genotype seen in female patients (57%)

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Summary

Introduction

Introduction The prevalence of2R/2R TYMS genotype is variable but estimated to be around 20–30% in Caucasians. The clinical relevance of TYMS 2R/2R genotype in predicting severe fluoropyrimidine-related adverse events (FrAE) is controversial. We explored the prevalence and clinical relevance of 2R/2R TYMS genotype. There are three fluoropyrimidine drugs in clinical use: intravenous 5fluorouracil (5-FU), oral capecitabine, and oral tegafur. Fluoropyrimidines are considered the backbone of most chemotherapeutic regimens approved for the treatment of gastrointestinal (GI) malignancies [3]. They represent treatment options in other malignancies such as breast and head and neck cancer [4, 5]. Among patients treated with 5-FU or capecitabine, approximately 20–25% of patients experience severe (grade 3–4) fluoropyrimidine-related adverse events (FrAEs) [6].

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