The prevalence and clinical relevance of 2R/2R TYMS genotype in patients with gastrointestinal malignancies treated with fluoropyrimidine-based chemotherapy regimens

Introduction The 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. Methods Between 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. Results The 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). Conclusion The 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.


Introduction
Fluoropyrimidines are antimetabolite chemotherapy drugs that are widely used in the treatment of cancer. There are three fluoropyrimidine drugs in clinical use: intravenous 5fluorouracil (5-FU), oral capecitabine, and oral tegafur. Capecitabine and tegafur are precursors of 5-FU [1,2]. Fluoropyrimidines are considered the backbone of most chemotherapeutic regimens approved for the treatment of gastrointestinal (GI) malignancies [3]. They also 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]. Severe FrAEs lead to patients' hospitalization and treatment interruption or discontinuation. The inter-individual variation in the occurrence and severity of FrAEs is partly due to genetic factors [7,8].
Dihydropyrimidine dehydrogenase (DPD) enzyme, encoded by DPYD gene, is the rate-limiting enzyme for 5-FU catabolism, eliminating approximately 80% of administered or formed 5-FU [9]. Any variation in DPD activity can result in a cytotoxic accumulation of free 5-FU. The prevalence of DPD deficiency in Caucasians is approximately 3-5% [10,11]. African Americans, especially women, seem to have a higher prevalence of approximately 4-12% [12]. Genomic analysis of patients with DPD deficiency has identified over 128 mutations and polymorphisms in the DPYD gene, but only four high-risk variants (DPYD*2A, DPYD*13, DPYD*9B, and HapB3) have been consistently associated with DPD deficiency and FrAEs. Genotyping for DPYD helps in identifying patients with DPD deficiency and guide the dosing of fluoropyrimidines. However, genotyping is limited to high-risk variants, and most patients who experience FrAEs are not DPD deficient [13][14][15].
In addition to DPYD, polymorphism in the TYMS gene that encodes thymidylate synthase (TS) may be associated with increased risk of FrAEs. TS is potently inhibited by 5-FU. Cells convert 5-FU to the metabolite fluorodeoxyuridine monophosphate, which binds to TS and inhibits the production of deoxythymidine monophosphate (dTMP). dTMP is essential for DNA replication and repair, so the lack of it leads to cell death [16,17]. Fig. 1 shows the cascade of metabolic reactions where fluoropyrimidines inhibit TS and eventually lead to DNA damage.
TYMS gene expression is regulated by transcription factors that bind to the promoter region. The 5′ untranslated region contains a 28-base-pair variable number of tandem repeats (VNTRs), which act to enhance the promoter and transcriptional activity (Fig. 2). Most patients have either 2 (2R) or 3 (3R) repeats. Homozygous TYMS 3R/3R genotype has a higher level of TS, while homozygous TYMS 2R/2R genotype has low TS level and may be at greater risk of FrAEs [18,19]. A single-nucleotide polymorphism of the second repeat of the 3R allele (3RC) abolishes a binding site in the 3R second repeat allele and reduces TS activity compared to wild-type 3R allele (3RG) [20].
The prevalence of 2R/2R TYMS genotype in different ethnic background is variable but estimated to be around 20-30% in Caucasians [21]. The clinical relevance of TYMS 2R/2R genotype in predicting severe FrAEs is controversial [7,19,[22][23][24][25][26]. Here, in a cohort of patients with GI malignancies treated with fluoropyrimidine-based chemotherapy regimens, we explored the prevalence and clinical relevance of 2R/2R TYMS genotype. Moreover, given the different racial and sex background in our cohort, ethnic and sex differences were explored.

Patient population
This is a retrospective study conducted at the University of South Alabama Mitchell Cancer Institute in Mobile, Alabama, USA in collaboration with ARUP Laboratories, The University of Utah, Salt Lake City, Utah, USA. Cohort was identified through searching our cancer center tumor registry for patients with GI malignancies genotyped for TYMS gene between 2011 and 2018. The University of South Alabama Institutional Review Board (IRB) approved this study and the IRB-approved database provided a waiver of the requirement for informed consent and allowed for the publication of de-identified data.

Fluoropyrimidine-based chemotherapy
The fluoropyrimidine-based chemotherapy regimens that the patients in this cohort received include FOLFIRINOX, FOLFOX with or without bevacizumab, cetuximab or panitumumab, XELOX, FOLFIRI with or without bevacizumab, cetuximab or panitumumab, XELIRI with or without bevacizumab, cetuximab or panitumumab, FLOT, 5-FU and mitomycin, 5-FU and liposomal irinotecan, Fig. 1 Schematic representation of fluoropyrimidine-based drug metabolic pathway. The capecitabine and tegafur are the oral pre-pro and pro-drug, respectively, which in turn converted into 5-FU, while 5-FU is directly administered as IV. In normal condition of DPD and TS activity, maximum drug is eliminated from body while minimal amount is functionally active and inhibits the DNA and RNA synthesis leading to cell death during cancer treatment. Patients possessing the DPD deficiency show grade 3-4 toxicity as maximum drug is accumulated in the body that inhibit the TYMS. The TYMS 2R/2R genotype has low TS level and correlated with severe fluoropyrimidines-related adverse events. DPD dihydropyrimidine dehydrogenase, UP uridine phosphorylase, UK uridine kinase, TK thymidine kinase, TP thymidine phosphorylase, TS thymidylate synthetase, OPRT orotate phosphoribosyltransferase, RNR ribonucleotide reductase, NME1-NME2 nucleoside diphosphate kinase. capecitabine and gemcitabine, single agent 5-FU with or without concurrent radiotherapy, and capecitabine with or without concurrent radiotherapy.

Genotyping strategy
Genotyping strategies were quite variable. The most common genotyping strategy was to genotype patients prior to initiating treatment with fluoropyrimidines-based chemotherapy. Between 2016 and 2018, genotyping was conducted almost universally on all patients with GI malignancies treated with fluoropyrimidines-based chemotherapy. Prior to 2016, only 24 patients were genotyped and genotyping was conducted at the discretion of the treating medical oncologist. Those patients were genotyped either because they experienced toxicities or because they had significant comorbidities and their medical oncologist decided to do upfront genotyping.

TYMS genotyping
Germline DNA was obtained from peripheral blood specimens and genotyped TYMS gene in ARUP laboratories (Salt Lake City, UT, USA). The VNTRs of the 5'UTR flank of TYMS (rs45445694) and their additional single-nucleotide variant (SNV) G>C in the first repeat of the 2R allele (rs183205964, named 2RG or 2RC), the SNV G>C in the second repeat of the 3R allele (rs2863542, named 3RG or 3RC), and the 6 bp insertion in the second repeat of the 3R allele (rs538469385) (all located into the rs45445694 variant) were performed by polymerase chain reactionrestriction fragment length polymorphism. A 6-bp deletion variant at the 3′UTR region of TYMS (rs151264360) was genotyped as well.

Toxicity grading and statistical analysis
Demographic and clinical data were extracted from the patients' charts. FrAEs were graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (version 5.0). Association between dichotomous fluoropyrimidine-related toxicities and TYMS genotype was performed using Fisher's exact test. Analyses with p values ≤ 0.05 were considered significant. Tests were performed using GraphPad software QuickCalcs (GraphPad software 2016, San Diego, CA).

Patient characteristics
Between 2011 and 2018, a total of 126 patients with GI malignancies were genotyped for TYMS and had no identifiable high-risk DPYD variants. The baseline characteristics of the patients are summarized in Table 1. Median age is 59 years. Males represented 55% of the patients, while females represented 45%. In our cohort, 63% were Caucasian, 35% were African Americans, and 2% were other ethnicities (Hispanics, Asians, and Indian Americans). Colon adenocarcinoma represented the most common malignancy in our cohort. Other patients had anal squamous cell carcinoma, appendix adenocarcinoma, cholangiocarcinoma, esophageal adenocarcinoma, gastric adenocarcinoma, neuroendocrine tumor, pancreatic adenocarcinoma, and rectal adenocarcinoma. A fluorouracil-based chemotherapy regimen was administered in 74% of the patients, while 26% of the patients received a capecitabinebased chemotherapy regimen.

Sex differences
In our cohort, the distribution of 2R/3RG TYMS genotype was similar between males and females. The distribution of all other genotypes apart from 2R/2R and 3RG/3RC TYMS genotypes was more frequent in males than females. The 2R/2R TYMS genotype had a very unique sex distribution where 20 out of 31 patients (65%) were females. This is the only TYMS genotype where females were twice as common as males. In fact, among all the female patients in our cohort (N = 57), the 2R/2R TYMS genotype was present in 20 female patients (35%). Moreover, among patients with TYMS genotypes that predict decreased TS expression, 2R/ 2R TYMS genotype was the most common TYMS genotype seen in female patients (57%). Of note, the three patients with 4R containing TYMS genotypes (2R/4R, 3R/4R, and 4R/3RG) were all males. TYMS genotyping in patients with

Ethnic differences
Caucasians were the majority in both genotypes that predict decreased TS expression and in genotypes (3RG/ 3RG and 3RG/3RC) that predict increased TS expression. Among patients with TYMS genotypes that predict decreased TS expression, 2R/2R TYMS genotype was the most common TYMS genotype seen in African American patients (60%). Of note, the three patients with 4R containing TYMS genotypes (2R/4R, 3R/4R, and 4R/3RG) were all African Americans. There was minimal representation of other ethnic backgrounds in our cohort. TYMS genotyping in patients with GI malignancies with mixed racial background is summarized in Table 2. Asian. c Hispanic. Table 3 The frequency of grade 1-2 and grade 3-4 fluoropyrimidines-related adverse events in patients with TYMS genotypes that predict increased and decreased TS expression.     Statistical analysis was performed using Fisher's exact test.
The prevalence and clinical relevance of 2R/2R TYMS genotype in patients with gastrointestinal. . .

Discussion
The prevalence of 2R/2R TYMS genotype in different ethnic background is quite variable. In Caucasian Americans, the prevalence of 2R/2R TYMS genotype in infants with conotruncal heart defects and control group was 21% and 26%, respectively. In the same study, the prevalence of 2R/2R TYMS genotype in American Hispanics was 17% and 18%, respectively [27]. In children with acute lymphoblastic leukemia (ALL) and matched control, the prevalence of 2R/2R TYMS genotype, respectively, was 21% and 24% in the Netherlands, 21% and 21% in Germany, 25% and 24% in United kingdom, and 25% and 30% in Slovenia [28][29][30][31]. In patients with colorectal cancer, the prevalence of 2R/2R TYMS genotype was 18% in Hungary and 28% in Denmark [17,32]. Many studies have explored the prevalence of 2R/2R TYMS genotype in Hispanic population as well. In healthy volunteers from Argentina, the reported prevalence is 26% [33]. In Brazil, the prevalence of 2R/2R TYMS genotype in children with ALL and matched control was 26% and 18%, respectively, in one study and 21% and 24%, respectively, in another study [34,35]. In Mexico, the prevalence of 2R/ 2R TYMS genotype in patients with colorectal cancer and healthy subjects is 22% and 19%, respectively.
The prevalence of 2R/2R TYMS genotype in other ethnicities (Asians and Indians) showed lower reported prevalence compared to Caucasians and Hispanics. In children with ALL and matched control, the prevalence of 2R/2R TYMS genotype, respectively, was 16% and 0% in one study and 1% and 0% in another study from Indonesia. The prevalence was 2% and 2% in Singapore and 19% and 10% in India [36][37][38][39]. Table 6 summarizes several studies that explored the prevalence of 2R/2R TYMS genotype.
In our cohort of 126 patients, the prevalence of 2R/2R TYMS genotype was 24.6% of the total cohort and 44% of the patients with genotypes that predict decreased expression of TS. Among Caucasians (N = 80), 19 patients (24%) had 2R/2R TYMS genotype, which is not very different from the reported prevalence of 2R/2R TYMS genotype in Caucasians in America or Europe. Among African Americans (N = 43), 12 patients (28%) had 2R/2R TYMS genotype, which is slightly higher than the prevalence of 2R/2R TYMS genotype in Caucasians. The prevalence of 2R/2R TYMS genotype in African Americans is not well established. In one study that explored pharmacogenomics in patients with colorectal cancer, 36 patients were African Americans, and among this group, 25 patients (69%) had either 2R/2R or 2R/3R TYMS genotypes [40].
Our study has several limitations. This study represents a single-institution experience with limited cohort of ethnic diversity. Our cohort was made of Caucasians and African Americans for the most part, and only three patients were from other ethnic backgrounds (Asian, Hispanic, and Indian American). Our cohort is also quite heterogenous regarding the primary site of the tumor and stage. It is also important to recognize that this study is a retrospective study and there are inherent limitations with a retrospective analysis, particularly regarding selection bias. TYMS genotyping strategies were quite variable as TYMS genotyping was at the discretion of the treating medical oncologist, and the selected treatment included several different fluoropyrimidine-based regimens. The medical oncologists followed the recommended dose management guidelines per package insert when they managed FrAEs. However, they still had a degree of variation in their practice. The process of attributing an experienced toxicity to 5-FU or capecitabine when they were part of fluoropyrimidine-based chemotherapy regimens was quite challenging sometimes. Every effort was made to make that attribution as accurate as possible. The aforementioned limitations should be kept in mind prior to drawing any conclusions.

Conclusion
The prevalence of TYMS 2R/2R genotype in our cohort was 24.6%. Among Caucasians and African Americans, it was 24% and 28%, respectively. Polymorphism in the promoter region of TYMS gene that predict 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.
The 2R/2R TYMS genotype had a very unique sex and ethnic distribution. Among patients with TYMS genotypes that predict decreased TS expression (2R/2R, 2R/3RC, 3RC/ 3RC), 2R/2R TYMS genotype was the most common TYMS genotype seen in female patients (57%) and in African American patients (60%). The reported higher prevalence of 2R/2R TYMS genotype in female African American patients in our study might represent one possible explanation for why women, especially African Americans, experience more grade 3-4 FrAEs.

Compliance with ethical standards
Conflict of interest The authors declare that they have no conflict of interest.
Publisher's note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons. org/licenses/by/4.0/.