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01.03.2010 | Original Article

Contribution of dihydropyrimidinase gene alterations to the development of serious toxicity in fluoropyrimidine-treated cancer patients

verfasst von: Julie Fidlerova, Petra Kleiblova, Matej Bilek, Stanislav Kormunda, Zuzana Formankova, Jan Novotny, Zdenek Kleibl

Erschienen in: Cancer Chemotherapy and Pharmacology | Ausgabe 4/2010

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Abstract

Purpose

Decreased 5-fluorouracil catabolism has been considered a major factor contributing to fluoropyrimidine (FP)-related toxicity. Alterations in the dihydropyrimidine dehydrogenase gene coding for the first and rate-limiting enzyme of FP catabolic pathway could explain toxicity in only a limited proportion of FP-treated patients. The importance of gene variants in dihydropyrimidinase (DPYS) coding for subsequent catabolic enzyme of FP degradation is not fully understood.

Methods

We performed genotyping of DPYS based on denaturing high-performance liquid chromatography in 113 cancer patients including 67 with severe FP-related toxicity and 46 without toxicity excellently tolerating FPs treatment.

Results

We detected nine DPYS variants including four located in non-coding sequence (c.-1T>C, IVS1+34C>G, IVS1-58T>C, and novel IVS4+11G>T), four silent (c.15G>A, c.216C>T, and novel c.105C>T and c.324C>A), and one novel missense variant c.1441C>T (p.R481W). All novel alterations were detected once only in patients without toxicity. The c.-1T>C and IVS1-58T>C variants were found to modify the risk of toxicity. The CC carriers of the c.-1C alleles were at higher risk of mucositis (OR = 4.13; 95% CI = 1.51–11.31; P = 0.006) and gastrointestinal toxicity (OR = 3.54; 95% CI = 1.59–7.88; P = 0.002), whereas the presence of the IVS1-58C allele decreased the risk of gastrointestinal toxicity (OR = 0.4; 95% CI = 0.17–0.93; P = 0.03) and leucopenia (OR = 0.29; 95% CI = 0.08–1.01; P = 0.05).

Conclusions

Our results indicate that missense and nonsense variants in DPYS are infrequent, however, the development of serious primarily gastrointestinal toxicity could be influenced by non-coding DPYS sequence variants c.-1T>C and IVS1-58T>C.

The IVS2-62G > T variant (with MAF = 0.42 and 0.25 for overall and Caucasian subpopulation, respectively in Thomas et al. study) was not detected in our population being localized outside DNA sequence amplified in amplicon covering exon 3 and flanking intronic sequences in our analysis.

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Titel: Contribution of dihydropyrimidinase gene alterations to the development of serious toxicity in fluoropyrimidine-treated cancer patients
verfasst von: Julie Fidlerova
Petra Kleiblova
Matej Bilek
Stanislav Kormunda
Zuzana Formankova
Jan Novotny
Zdenek Kleibl
Publikationsdatum: 01.03.2010
Verlag: Springer-Verlag
Erschienen in: Cancer Chemotherapy and Pharmacology / Ausgabe 4/2010
Print ISSN: 0344-5704
Elektronische ISSN: 1432-0843
DOI: https://doi.org/10.1007/s00280-009-1071-0

Springer Medizin

Contribution of dihydropyrimidinase gene alterations to the development of serious toxicity in fluoropyrimidine-treated cancer patients