Thymine as potential biomarker to predict 5-FU systemic exposure in patients with gastro-intestinal cancer: a prospective pharmacokinetic study (FUUT-trial)

被引:0
作者
Hanrath, Maarten A. [1 ]
Banken, Evi [2 ,10 ]
van den Wildenberg, Sebastian A. H. [3 ,4 ]
van de Kerkhof, Daan [3 ,4 ]
Moes, Dirk Jan A. R. [5 ]
Boisdron-Celle, Michele [6 ]
van den Bosch, Bianca J. C. [7 ]
Bax, Ramon [2 ]
Bet, Pierre M. [8 ]
Maring, Jan Gerard [9 ]
Creemers, Geert-Jan M. [2 ]
van Hellemond, Irene. E. G. [2 ]
Deenen, Maarten J. [1 ,5 ]
机构
[1] Catharina Hosp, Dept Clin Pharm, Eindhoven, Netherlands
[2] Catharina Hosp, Dept Med Oncol, Eindhoven, Netherlands
[3] Catharina Hosp, Dept Clin Chem, Eindhoven, Netherlands
[4] Eindhoven Univ Technol, Dept Biomed Engn, Lab Chem Biol, Eindhoven, Netherlands
[5] Leiden Univ, Med Ctr, Dept Clin Pharm & Toxicol, Leiden, Netherlands
[6] Western Canc Inst Paul Papin, Dept Oncopharmacol Pharmacogenet, INSERM, U892, Angers, France
[7] Maastricht Univ Med Ctr MUMC, Dept Clin Genet, Maastricht, Netherlands
[8] Univ Amsterdam, Dept Clin Pharmacol & Pharm, Med Ctr, Amsterdam, Netherlands
[9] Isala, Dept Clin Pharm, Zwolle, Netherlands
[10] Maastricht Univ, GROW Res Inst Oncol & Reprod, Maastricht, Netherlands
关键词
Gastrointestinal cancer; 5-Flurouracil; Endogenous DPD substrates; Toxicity; Thymine; DIHYDROPYRIMIDINE DEHYDROGENASE-ACTIVITY; ADVANCED COLORECTAL-CANCER; DEFICIENT PATIENTS; MONONUCLEAR-CELLS; SEVERE TOXICITY; PLASMA RATIO; 5-FLUOROURACIL; URACIL; FLUOROURACIL; DPYD;
D O I
10.1007/s00280-025-04759-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeIn 20-30% of the patients, fluoropyrimidines (5-FU) based chemotherapy leads to severe toxicity, which is associated with dihydropyridine dehydrogenase (DPD) deficiency. Therefore, DPYD genotyping became standard practice before treatment with fluoropyrimidines. Nevertheless, only 17% of the patients with severe toxicity have a DPYD variant. Therefore, an urgent need persists to investigate other strategies contributing to prediction and prevention of toxicity. Endogenous DPD substrates are considered as potential biomarkers to predict toxicity, yet contradictional data exist on demonstrating uracil as a reliable biomarker. Thymine as biomarker for toxicity has been investigated less. The aim of this study was to determine the association between the concentrations of uracil, thymine dihydrouracil (DHU) and dihydrothymine (DHT), with the systemic drug exposure of 5-FU and DPD enzyme activity in patients treated with 5-FU.MethodsWe included 36 patients with gastrointestinal malignancy who received 5-FU infusion. DPYD genotyping was conducted before start of treatment. Blood samples for determining 5-FU, uracil and thymine concentrations during infusion and DPD enzyme activity were taken.ResultsWe found a significant correlation between the 5-FU systematic exposure and baseline thymine concentrations (R2 = 0.1468; p = 0.0402). DPD enzyme activity was significantly correlated with baseline thymine concentrations but no correlation was found between DPD enzyme activity and 5-FU systemic drug exposure.Conclusion5-FU dose individualization based on thymine concentrations could be a promising addition to DPYD genotyping to predict 5-FU-induced toxicity. Larger prospective trials are needed to examine thymine as predictor for toxicity in daily practice.Trial registrationTrial NL7539 at 'Overview of Medical Research in the Netherlands' (ID NL-OMON21471). Date of registration 19-02-2019.
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页数:13
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