Literature DB >> 27864592

Evaluation of 5-fluorouracil degradation rate and Pharmacogenetic profiling to predict toxicity following adjuvant Capecitabine.

Michela Roberto1, Adriana Romiti2, Andrea Botticelli2, Federica Mazzuca2, Luana Lionetto3, Giovanna Gentile3, Ida Paris2, Rosa Falcone2, Maria Bassanelli2, Francesca Romana Di Pietro2, Concetta Elisa Onesti2, Elisabetta Anselmi2, Serena Macrini2, Maurizio Simmaco3, Paolo Marchetti2.   

Abstract

BACKGROUND: On account of the lack of predictive biomarkers of toxicity, we investigated whether polymorphisms of genes involved in fluoropyrimidine metabolism and 5-fluorouracil (5-FU) degradation rate were associated with outcomes of adjuvant capecitabine in patients with early stage gastrointestinal cancers.
METHODS: Genotyping of DPYD GIVS14A, MTHFR C677T and A1298C SNPs were performed by pyro-sequencing technology. PCR analysis was used for genotyping TYMS-TSER. We also evaluated the 5-FU degradation rate, which determines the amount of drug consumed by PBMC in a time unit. Association of these variables with clinical outcome was evaluated using multivariate logistic regression analysis.
RESULTS: One hundred forty-two patients with early stage colon (39%), rectal (28%), stomach (20%) and pancreatic (13%) cancer, treated with adjuvant capecitabine, were included in this retrospective analysis. Seventy and 20% of the patients suffered from at least one G1-4 and G3-4 adverse events, respectively. According to the 5-FU degradation rate, three and 13 patients were assigned as poor (<0.86 ng/mL/106 cells/min) and ultra-rapid (>2.1 ng/mL/106 cells/min) metabolizers, respectively. At a multivariate logistic regression analysis, an altered 5-FU degradation rate (values <0.86 or >2.10 ng/mL/106 cells/min) was associated with grade 3-4 adverse events (OR = 2.09, 95% CI: 1.14-3.82, P = 0.01). No correlation was reported between toxicity and gene polymorphisms except for hand-foot syndrome that was more frequent in the MTHFR 1298CC homozygous variant genotype (OR = 2.03, 95% CI 1.04-3.96, P = 0.03).
CONCLUSIONS: 5-FU degradation rate may be regarded as possible predictive biomarker of capecitabine toxicity in early stage gastrointestinal cancer.

Entities:  

Keywords:  Adjuvant capecitabine; Gene polymorphisms; Oral fluoropyrimidines; Personalized medicine; Predictive biomarkers; Toxicity

Mesh:

Substances:

Year:  2016        PMID: 27864592     DOI: 10.1007/s00228-016-2160-8

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  22 in total

1.  Relationship between single nucleotide polymorphisms and haplotypes in DPYD and toxicity and efficacy of capecitabine in advanced colorectal cancer.

Authors:  Maarten J Deenen; Jolien Tol; Artur M Burylo; Valerie D Doodeman; Anthonius de Boer; Andrew Vincent; Henk-Jan Guchelaar; Paul H M Smits; Jos H Beijnen; Cornelis J A Punt; Jan H M Schellens; Annemieke Cats
Journal:  Clin Cancer Res       Date:  2011-04-15       Impact factor: 12.531

2.  The TYMS-TSER polymorphism is associated with toxicity of low-dose capecitabine in patients with advanced gastrointestinal cancer.

Authors:  Adriana Romiti; Michela Roberto; Chiara D'Antonio; Concetta E Onesti; Viola Barucca; Annalisa Milano; Giovanna Gentile; Luana Lionetto; Emanuela Medda; Federica Mazzuca; Andrea Botticelli; Rosa Falcone; Maurizio Simmaco; Paolo Marchetti
Journal:  Anticancer Drugs       Date:  2016-11       Impact factor: 2.248

3.  Germline TYMS genotype is highly predictive in patients with metastatic gastrointestinal malignancies receiving capecitabine-based chemotherapy.

Authors:  M Joerger; A D R Huitema; H Boot; A Cats; V D Doodeman; P H M Smits; L Vainchtein; H Rosing; I Meijerman; M Zueger; D Meulendijks; T D Cerny; J H Beijnen; J H M Schellens
Journal:  Cancer Chemother Pharmacol       Date:  2015-02-13       Impact factor: 3.333

4.  Role of genetic and nongenetic factors for fluorouracil treatment-related severe toxicity: a prospective clinical trial by the German 5-FU Toxicity Study Group.

Authors:  Matthias Schwab; Ulrich M Zanger; Claudia Marx; Elke Schaeffeler; Kathrin Klein; Jürgen Dippon; Reinhold Kerb; Julia Blievernicht; Joachim Fischer; Ute Hofmann; Carsten Bokemeyer; Michel Eichelbaum
Journal:  J Clin Oncol       Date:  2008-02-25       Impact factor: 44.544

5.  Thymidylate synthase gene polymorphism predicts toxicity in colorectal cancer patients receiving 5-fluorouracil-based chemotherapy.

Authors:  Thierry Lecomte; Jean-Marc Ferraz; Franck Zinzindohoué; Marie-Anne Loriot; David-Alexandre Tregouet; Bruno Landi; Anne Berger; Paul-Henri Cugnenc; Raymond Jian; Philippe Beaune; Pierre Laurent-Puig
Journal:  Clin Cancer Res       Date:  2004-09-01       Impact factor: 12.531

6.  Association of molecular markers with toxicity outcomes in a randomized trial of chemotherapy for advanced colorectal cancer: the FOCUS trial.

Authors:  Michael S Braun; Susan D Richman; Lindsay Thompson; Catherine L Daly; Angela M Meade; Julian W Adlard; James M Allan; Mahesh K B Parmar; Philip Quirke; Matthew T Seymour
Journal:  J Clin Oncol       Date:  2009-10-26       Impact factor: 44.544

7.  Pharmacogenetic profiling in patients with advanced colorectal cancer treated with first-line FOLFIRI chemotherapy.

Authors:  A Ruzzo; F Graziano; F Loupakis; D Santini; V Catalano; R Bisonni; R Ficarelli; A Fontana; F Andreoni; A Falcone; E Canestrari; G Tonini; D Mari; P Lippe; F Pizzagalli; G Schiavon; P Alessandroni; L Giustini; P Maltese; E Testa; E T Menichetti; M Magnani
Journal:  Pharmacogenomics J       Date:  2007-06-05       Impact factor: 3.550

8.  Methylenetetrahydrofolate reductase genetic polymorphisms and toxicity to 5-FU-based chemoradiation in rectal cancer.

Authors:  F Thomas; A A Motsinger-Reif; J M Hoskins; A Dvorak; S Roy; A Alyasiri; R J Myerson; J W Fleshman; B R Tan; H L McLeod
Journal:  Br J Cancer       Date:  2011-11-01       Impact factor: 7.640

9.  Pharmacogenetic variants in the DPYD, TYMS, CDA and MTHFR genes are clinically significant predictors of fluoropyrimidine toxicity.

Authors:  A Loganayagam; M Arenas Hernandez; A Corrigan; L Fairbanks; C M Lewis; P Harper; N Maisey; P Ross; J D Sanderson; A M Marinaki
Journal:  Br J Cancer       Date:  2013-06-04       Impact factor: 7.640

Review 10.  Genetic markers of toxicity from capecitabine and other fluorouracil-based regimens: investigation in the QUASAR2 study, systematic review, and meta-analysis.

Authors:  Dan Rosmarin; Claire Palles; David Church; Enric Domingo; Angela Jones; Elaine Johnstone; Haitao Wang; Sharon Love; Patrick Julier; Claire Scudder; George Nicholson; Anna Gonzalez-Neira; Miguel Martin; Daniel Sargent; Erin Green; Howard McLeod; Ulrich M Zanger; Matthias Schwab; Michael Braun; Matthew Seymour; Lindsay Thompson; Benjamin Lacas; Valérie Boige; Nuria Ribelles; Shoaib Afzal; Henrik Enghusen; Søren Astrup Jensen; Marie-Christine Etienne-Grimaldi; Gérard Milano; Mia Wadelius; Bengt Glimelius; Hans Garmo; Milena Gusella; Thierry Lecomte; Pierre Laurent-Puig; Eva Martinez-Balibrea; Rohini Sharma; Jesus Garcia-Foncillas; Zdenek Kleibl; Alain Morel; Jean-Pierre Pignon; Rachel Midgley; David Kerr; Ian Tomlinson
Journal:  J Clin Oncol       Date:  2014-03-03       Impact factor: 50.717

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  6 in total

Review 1.  Pharmacogenetic profiling and individualised therapy in the treatment of degenerative spinal conditions.

Authors:  Jake M McDonnell; Brian Rigney; James Storme; Daniel P Ahern; Gráinne Cunniffe; Joseph S Butler
Journal:  Ir J Med Sci       Date:  2022-08-13       Impact factor: 2.089

2.  Importance of Rare DPYD Genetic Polymorphisms for 5-Fluorouracil Therapy in the Japanese Population.

Authors:  Eiji Hishinuma; Yoko Narita; Kai Obuchi; Akiko Ueda; Sakae Saito; Shu Tadaka; Kengo Kinoshita; Masamitsu Maekawa; Nariyasu Mano; Noriyasu Hirasawa; Masahiro Hiratsuka
Journal:  Front Pharmacol       Date:  2022-06-15       Impact factor: 5.988

3.  Polymorphisms in TYMS for Prediction of Capecitabine-Induced Hand-Foot Syndrome in Chinese Patients with Colorectal Cancer.

Authors:  Si-Qi Dong; Tong-Min Wang; Jiang-Bo Zhang; Yong-Qiao He; Wen-Qiong Xue; Zi-Yi Wu; Da-Wei Yang; Lian-Jing Cao; Jing-Wen Huang; Xi-Zhao Li; Pei-Fen Zhang; Xiao-Hui Zheng; Wei-Hua Jia
Journal:  Cancer Res Treat       Date:  2020-12-02       Impact factor: 4.679

4.  Drug-Drug Interactions and Pharmacogenomic Evaluation in Colorectal Cancer Patients: The New Drug-PIN® System Comprehensive Approach.

Authors:  Michela Roberto; Alessandro Rossi; Martina Panebianco; Leda Marina Pomes; Giulia Arrivi; Debora Ierinò; Maurizio Simmaco; Paolo Marchetti; Federica Mazzuca
Journal:  Pharmaceuticals (Basel)       Date:  2021-01-15

5.  A Meta-Analysis: Methylenetetrahydrofolate Reductase C677T Polymorphism in Gastric Cancer Patients Treated with 5-Fu Based Chemotherapy Predicts Serious Hematologic Toxicity but Not Prognosis.

Authors:  Cheng Tang; Shan Yu; Huiqin Jiang; Wei Li; Xiaojing Xu; Xi Cheng; Ke Peng; Erbao Chen; Yuehong Cui; Tianshu Liu
Journal:  J Cancer       Date:  2018-02-28       Impact factor: 4.207

Review 6.  Individualized Dosing of Fluoropyrimidine-Based Chemotherapy to Prevent Severe Fluoropyrimidine-Related Toxicity: What Are the Options?

Authors:  Jonathan E Knikman; Hans Gelderblom; Jos H Beijnen; Annemieke Cats; Henk-Jan Guchelaar; Linda M Henricks
Journal:  Clin Pharmacol Ther       Date:  2020-11-12       Impact factor: 6.875

  6 in total

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