Evaluation of adverse effects of chemotherapy regimens of 5-fluoropyrimidines derivatives and their association with DPYD polymorphisms in colorectal cancer patients

Background 5-Fluorouracil (5-FU) and capecitabine are fluoropyrimidine derivatives that mainly metabolized with dihydropyrimidine dehydrogenase enzyme (DPD). The genetic polymorphism in the genes encoding this enzyme may result in a decrease or loss of enzyme activity which may lead to the accumulation of medicines, their metabolites and potential toxicity. Method This cross-sectional study was conducted on 88 participants with colorectal cancer (CRC). After DNA extraction, polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method was used to determine the DPD gene (DPYD) polymorphisms including IVS 14 + 1 G > A, 2846 A > T and 2194 G > A. Chemotherapy-induced side effects were evaluated according to the Common Terminology Criteria for Adverse Events (CTCAE Version 5.0). Result Data were collected from 227 chemotherapy cycles of 88 patients with CRC. In a comparison of FOLFOX and FOLFIRI regimens, there was no significant difference in the occurrence of chemotherapy-induced diarrhea, nausea, vomiting and oral mucositis. However, the peripheral neuropathy was more frequent in patients who were treated with FOLFOX (P <  0.001) and hair loss was more common in patients who received FOLFIRI regimen (P = 0.048). Incidence of the DPD IVS14 + 1 G > A polymorphism was observed in four patients (5.5%). There was no association between IVS14 + 1 G > A polymorphism and the occurrence of adverse reactions. Conclusion FOLFOX and FOLFIRI were the most common regimens in CRC patients and their toxicity profile was different in some adverse reactions. Prevalence of IVS14 + 1G > A variant was relatively higher than other similar studies. Trial registration Approval code; IR.MAZUMS.REC.95.2480.


Background
Nearly 50,000 incident cancer cases are reported in Iran annually. It has been reported that gastrointestinal (GI) cancers have the highest incidence rate in Iran [1]. CRC is the third most frequent cancer in the worldwide and is ranked third in terms of mortality [2]. There are different types of cancer treatments, including surgery, targeted therapies, and chemotherapy. The choice of therapy depends upon several factors such as tumor stage, molecular tumor indices, and functional status of the patient [3]. Fluoropyrimidine derivatives including 5-FU and capecitabine (prodrug of 5-FU) inhibit the synthesis of thymidylate synthase (TS) leading to inhibition of synthesis of purine and pyrimidine bases [4][5][6]. 5-FU is a cytotoxic chemotherapy medicine that is widely used in the treatment of a variety of cancers, including colon, rectum, breast, stomach, and pancreas [7]. A substantial number of enzymes are involved in the metabolism of 5-FU, First, thymidine phosphorylase (TP) catalyzes the conversion of 5-FU to its active metabolite, 5-fluoro-2′deoxyuridine. Subsequently, 5′-fluoro-2-deoxyuridine converts to its active metabolite 5-fluoro-2′-deoxyuridine 5′-monophosphate (FdUMP) through phosphorylation by the thymidine kinase. FdUMP forms a ternary complex with methylene tetrahydrofolate and TS which finally lead to the inhibition of DNA synthesis. By inhibiting the participation of uracil in RNA, the complex will also inhibit RNA synthesis [5][6][7][8]. DPD is an enzyme present in the liver and accountable for about 80-85% of 5-FU catabolism. DPD catabolizes 5-FU to 5,6-dihydro-5-fluorouracil (DHFU) [5][6][7][8][9]. DPD deficiency can be associated with an exacerbation of diarrhea, nausea, vomiting, mucositis, and neurotoxicity of fluoropyrimidine derivatives [10]. The DPD enzyme is encoded by the DPYD and several single nucleotide polymorphisms (SNP) including IVS14 + 1G > A, 464 T > A, 2194 G > A, 496 A > G, and 1627 A > G have been reported in the DPYD [11][12][13]. DPYD deficiency following absence or mutation of the allele reduces the 5-FU clearance and may increase the risk of developing severe toxicity. Mutation in some variants such as IVS14 + 1 G > A, 2846 A > T and 2194 G > A may lead to reduced DPD enzyme levels [14].
The most common type of genetic polymorphism reported in patients with CRC that leads to a decrease or elimination of the activity of the DPD enzyme is mutation from guanine to adenine in DPYD of intron 14 called rs3918290 or IVS14 + 1G > A or * 2 A [15]. In addition to IVS14 + 1G > A, other polymorphisms including 464 T > A and 2194 G > A have also been associated with 5-FU side effects such as bone marrow depression and digestive tract complications [16]. Different chemotherapy regimens have been used in the treatment of CRC including FOLFOX (5-FU; 400 mg/m 2 IV   bolus over 5 min and 2400 mg/m 2 IV over 46 h; leucovorin 400 mg/m 2 IV day 1 and oxaliplatin 85 mg/m 2 IV  day 1), FOLFIRI (5-FU 400 mg/m2 IV bolus over 5 min  and 2400 mg/m2 IV over 46 h; leucovorin 400 mg/m 2 IV  and irinotecan 180 mg/m 2 IV), and XELOX (capecitabine 1000 mg/m2 twice daily for 14 of every 21 days and oxaliplatin 130 mg/m 2 on day 1) [17,18].
The frequency of occurrence and severity of side effects of 5-FU and capecitabine may vary according to the type of chemotherapy regimen and interpersonal differences in the expression of genes encoding enzymes involved in the metabolism of drugs.
Further studies are required to have a better understanding of the association between DPYD polymorphism and the side effects of chemotherapy regimens of 5-FU derivatives [19]. This study aimed to evaluate the adverse effects of different chemotherapy regimens used in CRC patients and the relationship between genetic polymorphism of DPYD and the adverse effects of chemotherapy regimens in a sample of CRC patients in the north of Iran.

Methods
From October of 2016 to June of 2017, this crosssectional study was carried out in outpatient oncology clinic of Imam Khomeini Hospital, Sari, Mazandaran. Eighty-eight patients with colon or rectal cancer were randomly assigned to receive either 5-FU or capecitabine in common chemotherapy regimens in use for CRC, including FOLFOX and FOLFIRI. Some of the patients were unable to continue the study due to different reasons including the changing of the medical center, discontinuing chemotherapy regimen, and death. Consequently, 73 patients were enrolled in this study. The study was approved by the Mazandaran University of Medical Sciences (MAZUMS) Review Board and all patients were given informed consent prior to participation in the study. The demographic and clinical data of patients including age, sex, tumor location, TNM stage (Tumor size, Lymph nodes involvement, Metastasis) and chemotherapy regimen were recorded.
Two milliliters of peripheral blood were collected from each participant and transferred to EDTA-containing tubes and then stored in a freezer at − 80°C until time of analysis.
Three SNP of DPYD gene including IVS14 + 1 G > A, 2194 A > G and 2846 A > T were studied based on PCR-RFLP method.
Genomic DNA was extracted from peripheral blood using the QIA Amp DNA Mini kit (Qiagen, Germany). PCR-RFLP method was used to determine the IVS14 + 1 G > A and 2846 A > T variants applying Mae II and Bse8I restriction enzymes, respectively. Tetra-primer ARMS-PCR was optimized to detect the 2194 G > A variant.
Amplification performed with an initial denaturation step (5 min at 95°C) followed by 35 cycles of 95°C for 1 min, 60°C for 1 min for IVS14 + 1 G > A variant, 62°C for 2846 A > T, 58°C for 2846 A > T variants, and then 72°C for 1 min followed by an extension step of 72°C for 5 min [20].
Side effects experienced by patients including diarrhea, nausea, vomiting, mucositis, peripheral neuropathy, and hair loss were recorded and graded according to CTCAE Version 5.0 [21].
Data analysis was performed using SPSS 24 software. Mean and standard deviation was reported for quantitative data and qualitative dichotomous data were presented as frequency and percent. Comparison of qualitative data was done using Chi-square test. In all cases, P < 0.05 was considered a statistically significant difference.

Results
The demographic and clinical characteristics of patients are presented in Table 1. The colon cancer incidence was more frequent compared to rectal cancer incidence. Most patients had a disease with a TNM stage of 3 or 4 (71%). FOLFOX (72.7%) and FOLFIRI (20.8%) were the most used regimens compared to other chemotherapy regimens (93.5% versus 6.5%).
IVS14 + 1G > A polymorphism was found in 4 of 73 patients (5.5%), all of which were heterozygous. There were no cases of two other polymorphisms (2846 A > T and 2194 G > A).
The frequencies of chemotherapy-related side effects were summarized in Table 3.
Patients treated with FOLFOX showed higher rate of peripheral neuropathy (96% versus 76.6%, P < 0.001), whereas FOLFIRI regimen was associated with a higher occurrence of hair loss (58.5% vs. 40%, P = 0.04). The rate of other adverse effects including diarrhea, nausea, vomiting and oral mucositis were not different. The severity of the side effects experienced with each of the chemotherapy cycles was presented in the Table 4.
The grading of most of the adverse reactions was not statistically different for FOLFOX and FOLFIRI regimens, except hair loss. A higher grade toxicity (grade 2) was more common with FOLFIRI compared to FOLFOX (20.8% versus 5.4%, P = 0.034). In the case of diarrhea, 5 out of 41 patients who received FOLFIRI (12%) and 13 out of 140 patients who received FOLFOX (9.2%) experienced grade 3/ 4 diarrhea (P = 0.95). Grade 3 nausea was observed only in one case of FOLFOX regimen and there was not any Grade 3 or 4 nausea with FOLFIRI regimen (P = 0.32). Vomiting Grade 3/4 was observed in 14.3 and 11.1% of patients received FOLFOX and FOLFIRI, respectively (P = 0.9). Grade 3/4 oral mucositis occurred in 11.4 and 16.7% of patients treated with FOLFOX and FOLFIRI, respectively (P = 0.59). Peripheral neuropathy was a common adverse effect with both FOLFOX and FOLFIRI regimens, but almost all patients experienced Grade 1 or 2 toxicity. Grade 3 toxicity of peripheral neuropathic symptom occurred only in one patient with a FOLFOX regimen (P = 0.39).
The incidence of adverse drug reactions considering IVS14 + 1G > A polymorphism was presented in Table 5. Diarrhea, vomiting, oral mucositis, peripheral neuropathy, and hair loss were not different between patients with and without IVS14 + 1G > A polymorphism.
All of the patients with IVS14 + 1G > A polymorphism showed hair loss, whereas 50.7% of patients who did not have this polymorphism experienced this side effect (P = 0.093).
There was no significant difference between the presence or absence of IVS14 + 1G > A polymorphism with incidence of diarrhea (25% vs. 23.2%; P = 0.663), nausea Common symptoms reported were diarrhea (12%), neutropenia (11.7%), nausea and vomiting (5%), fatigue (4.9%), and mucositis (4.2%) [25]. In this study, the prevalence of diarrhea, nausea, vomiting, oral mucositis, peripheral neuropathy, and hair loss was 24.7, 30.8, 19.4, 34.4, 92.1 and 46.7%, respectively. We did not find any  Patients were received regimes containing Oxaliplatin and Capecitabine and the prevalence of IVS14 + 1G > A polymorphism was 1%, that was less than the amount detected in our study. The results showed a significant correlation between polymorphisms and side effects of  Capecitabine. Five out of seven of the patients with IVS141G > A polymorphism experienced diarrhea (71%). All patients with IVS141G > A polymorphism showed Grade 3 or 4 diarrhea symptoms [13]. Unlike our study, He et al. did not see the IVS14 + 1G > A polymorphism in 142 Chinese patients with colorectal and nasopharyngeal cancers [26].
In a study conducted by Uzunkoy et al. in 2007 on 56 patients with CRC cancer in Turkey, they found two cases of IVS14 + 1G > A polymorphism (0.6%), both of which were heterozygous [27]. The rate of IVS14 + 1G > A heterozygous polymorphism was less in their study compared to our population studied.
In a study conducted by Raida et al. in Germany, of 851 Caucasian patients with CRC treated with 5-FU, the prevalence of IVS14 + 1G > A was 0.94%, all of which were heterozygous, and approximately 25% of those who experienced Grade 3 and 4 had this polymorphism [28]. The prevalence of IVS14 + 1G > A polymorphism was higher in our population. Different populations and races show different prevalence of IVS14 + 1G > A polymorphism in the DPYD [29]. In a study on 72 patients in Taiwan, 2.7% of patients had IVS14 + 1G > A polymorphism in the DPYD [30]. However, in another study on 262 patients in Taiwan, this polymorphism was not observed [31]. DPD enzyme activity was reported to be higher than normal in North Korea [8] that may influence the efficacy and toxicity of fluoropyrimidine-based adjuvant chemotherapy.
In addition to IVS14 + 1G > A polymorphism, in this study we also examined the presence of other DPYD polymorphism including A > T 2846 and 2194 G > A, but these polymorphisms were not observed in our patients. Lee et al. reported that the prevalence of A > T 2846 polymorphism in 2886 Caucasian patients with Grade 3 colon cancer who received FOLFOX and FOLFIRI regimens was about 1.1% [25]. In a study by Terrazzino et al. on 2308 patients, the prevalence of 2846 A > T polymorphisms was 0.2% [32].
Deenen et al. reported that 2194 G > A polymorphism in 568 Dutch patients with CRC receiving the XELOX regimen was about 7%, and they observed the relationship between severity of diarrhea (Grade 3/4) and 2194 G > A polymorphism [13]. But in another study conducted on 142 Chinese patients with colorectal and nasopharyngeal cancers receiving 5-FU-treated regimens, the prevalence of the 2194 G > A polymorphism was reported 1.4% and there was not any relationship with the DPD enzyme activity [26]. Although efforts have been made to determine the association between the DPYD and the 5-FU toxicities, it seems that DPYD alone can detect approximately 20% of the early side effects of 5FU [15]. Present study shows that there was no significant correlation between IVS14 + 1G > A polymorphism and the profile of side effects of 5-FU in CRC patients. It other words, a major part of the symptoms experienced by patients is independent of DPYD polymorphism. But the results of our study should be interpreted cautiously as the sample size of our study was small and the relevant SNPs was only observed in four cases.

Conclusion
Among the studied polymorphisms, only the IVS14 + 1G > A polymorphism was found in our patients and its prevalence was somewhat higher than the similar studies. Two other polymorphisms including 2194 G > A and 2846 A > T were not found. FOLFOX and FOLFIRI regimens were used more than other regimens. The profile of toxicities of FOLFOX and FOLFIRI regimens was different in some adverse reactions such as peripheral neuropathy and alopecia and we did not observe any relationship between adverse reactions and DPYD polymorphism.