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The role of pharmacogenetics in capecitabine efficacy and toxicity

https://doi.org/10.1016/j.ctrv.2016.08.001
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Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

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The 65 checked references that resolve
resolves10.1007/s10120-013-0297-z
Optimal chemotherapy for advanced gastric cancer: is there a global consensus?
resolves10.3816/CCC.2010.n.004
Evolution of Capecitabine Dosing in Colorectal Cancer
resolves10.3816/CBC.2010.n.017
Evolution of Capecitabine Dosing in Breast Cancer
resolves10.1007/s12032-011-9958-0
5-Fluorouracil or capecitabine in the treatment of advanced colorectal cancer: a pooled-analysis of randomized trials
resolves10.1093/annonc/mdp047
Meta-analysis of the REAL-2 and ML17032 trials: evaluating capecitabine-based combination chemotherapy and infused 5-fluorouracil-based combination chemotherapy for the treatment of advanced oesophago-gastric cancer
resolves10.1016/j.clbc.2012.10.002
Making Capecitabine Targeted Therapy for Breast Cancer: Which is the Role of Thymidine Phosphorylase?
resolves10.1111/bcp.12449
Incidence and relative risk of grade 3 and 4 diarrhoea in patients treated with capecitabine or 5‐fluorouracil: a meta‐analysis of published trials
resolves10.1016/j.ctrv.2013.03.005
Cardiotoxicity in cancer patients treated with 5-fluorouracil or capecitabine: A systematic review of incidence, manifestations and predisposing factors
resolves10.1016/j.clbc.2011.06.005
Dose-Adjusting Capecitabine Minimizes Adverse Effects While Maintaining Efficacy: A Retrospective Review of Capecitabine for Metastatic Breast Cancer
resolves10.1016/j.ejca.2015.10.013
Renal function, body surface area, and age are associated with risk of early-onset fluoropyrimidine-associated toxicity in patients treated with capecitabine-based anticancer regimens in daily clinical care
resolves10.2217/pgs.11.72
Dihydropyrimidine Dehydrogenase Gene as a Major Predictor of Severe 5-Fluorouracil Toxicity
resolves10.1038/ncponc1240
Capecitabine: have we got the dose right?
resolves10.1046/j.1365-2125.2003.01765.x
Population pharmacokinetics and concentration–effect relationships of capecitabine metabolites in colorectal cancer patients
resolves10.1038/clpt.2013.172
Clinical Pharmacogenetics Implementation Consortium Guidelines for Dihydropyrimidine Dehydrogenase Genotype and Fluoropyrimidine Dosing
resolves10.1097/FPC.0b013e32833c6107
PharmGKB summary
resolves10.1124/jpet.104.081265
Hydrolysis of Capecitabine to 5′-Deoxy-5-fluorocytidine by Human Carboxylesterases and Inhibition by Loperamide
resolves10.1159/000074480
Forced Expression of Cytidine Deaminase Confers Sensitivity to Capecitabine
resolves10.1517/17425255.2015.985648
Role of cytidine deaminase in toxicity and efficacy of nucleosidic analogs
resolves10.1007/s00280-008-0889-1
Early severe toxicities after capecitabine intake: possible implication of a cytidine deaminase extensive metabolizer profile
resolves10.1200/JCO.2011.37.9289
Sudden Death Related to Toxicity in a Patient on Capecitabine and Irinotecan Plus Bevacizumab Intake: Pharmacogenetic Implications
resolves10.1007/s002800050043
Preferential activation of capecitabine in tumor following oral administration to colorectal cancer patients
resolves10.2165/00003088-200140020-00002
Clinical Pharmacokinetics of Capecitabine
resolves10.1111/j.1365-2125.2008.03159.x
Candidate mechanisms for capecitabine‐related hand–foot syndrome
resolves10.1038/nrc1074
5-Fluorouracil: mechanisms of action and clinical strategies
resolves10.1016/j.gene.2013.09.063
Folate: Metabolism, genes, polymorphisms and the associated diseases
resolves10.1158/1535-7163.MCT-08-0219
<i>Thymidylate synthase</i>gene variations: predictive and prognostic markers
resolves10.1634/theoncologist.2010-0261
Part 4: Pharmacogenetic Variability in Anticancer Pharmacodynamic Drug Effects
resolves10.2217/pgs.13.118
Current Approaches for <i>TYMS</i> Polymorphisms and their Importance in Molecular Epidemiology and Pharmacogenetics
resolves10.1158/1078-0432.CCR-06-0320
Pharmacogenetics of Capecitabine in Advanced Breast Cancer Patients
resolves10.1093/annonc/mdr445
The Cyclin D1 (CCND1) A870G polymorphism predicts clinical outcome to lapatinib and capecitabine in HER2-positive metastatic breast cancer
resolves10.1002/ijc.29694
Increased risk of severe fluoropyrimidine-associated toxicity in patients carrying a G to C substitution in the first 28-bp tandem repeat of the thymidylate synthase 2R allele
resolves10.2217/14622416.9.9.1195
Pharmacogenetic Relevance of <i>MTHFR</i> Polymorphisms
resolves10.1016/j.ejca.2015.11.008
Prospective DPYD genotyping to reduce the risk of fluoropyrimidine-induced severe toxicity: Ready for prime time
resolves10.1200/JCO.2015.63.1325
Upfront Genotyping of <i>DPYD</i>*<i>2A</i> to Individualize Fluoropyrimidine Therapy: A Safety and Cost Analysis
resolves10.1007/s00280-007-0493-9
Functional study of the 830C&gt;G polymorphism of the human carboxylesterase 2 gene
resolves10.1007/s10549-013-2516-z
Fixed-dose capecitabine is feasible: results from a pharmacokinetic and pharmacogenetic study in metastatic breast cancer
resolves10.2217/pgs.13.56
<i>CDA</i> Gene Polymorphisms and Enzyme Activity: Genotype–phenotype Relationship in an Italian–Caucasian Population
resolves10.1007/s003840100358
Thymidylate synthase gene polymorphism predicts response to capecitabine in advanced colorectal cancer
resolves10.1007/s12094-012-0979-8
Polymorphism of TS 3′-UTR predicts survival of Chinese advanced gastric cancer patients receiving first-line capecitabine plus paclitaxel
resolves10.1007/s00280-015-2698-7
Germline TYMS genotype is highly predictive in patients with metastatic gastrointestinal malignancies receiving capecitabine-based chemotherapy
resolves10.1093/annonc/mdq572
Pharmacogenetic interaction analysis for the efficacy of systemic treatment in metastatic colorectal cancer
resolves10.1158/1078-0432.CCR-07-0425
Thymidylate Synthase and Methylenetetrahydrofolate Reductase Gene Polymorphisms and Toxicity to Capecitabine in Advanced Colorectal Cancer Patients
resolves10.1158/1078-0432.CCR-10-2209
Relationship between Single Nucleotide Polymorphisms and Haplotypes in <i>DPYD</i> and Toxicity and Efficacy of Capecitabine in Advanced Colorectal Cancer
resolves10.2174/138920008784220646
A Carboxylesterase 2 Gene Polymorphism as Predictor of Capecitabine on Response and Time to Progression
resolves10.1634/theoncologist.2014-0379
Standard Versus Continuous Administration of Capecitabine in Metastatic Breast Cancer (GEICAM/2009-05): A Randomized, Noninferiority Phase II Trial With a Pharmacogenetic Analysis
resolves10.1007/s00280-009-0947-3
Prostaglandin synthase 2/cyclooxygenase 2 (PTGS2/COX2) 8473T&gt;C polymorphism associated with prognosis for patients with colorectal cancer treated with capecitabine and oxaliplatin
resolves10.1007/s00432-012-1183-5
Pharmacogenetic assessment of clinical outcome in patients with metastatic breast cancer treated with docetaxel plus capecitabine
resolves10.1002/cncr.26737
Identification of novel germline polymorphisms governing capecitabine sensitivity
resolves10.1097/FPC.0000000000000119
Clinical validation study of genetic markers for capecitabine efficacy in metastatic colorectal cancer patients
resolves10.18632/oncotarget.3289
Variants in<i>CDA</i>and<i>ABCB1</i>are predictors of capecitabine-related adverse reactions in colorectal cancer
resolves10.1200/JCO.2013.51.1857
Genetic Markers of Toxicity From Capecitabine and Other Fluorouracil-Based Regimens: Investigation in the QUASAR2 Study, Systematic Review, and Meta-Analysis
resolves10.1158/1078-0432.CCR-10-1741
A Polymorphism in the <i>Cytidine Deaminase</i> Promoter Predicts Severe Capecitabine-Induced Hand-Foot Syndrome
resolves10.1007/s00280-015-2872-y
Phase 1a/1b and pharmacogenetic study of docetaxel, oxaliplatin and capecitabine in patients with advanced cancer of the stomach or the gastroesophageal junction
resolves10.4161/cbt.2.4.424
A Novel Function for the rTS gene
resolves10.1038/bjc.2013.262
Pharmacogenetic variants in the DPYD, TYMS, CDA and MTHFR genes are clinically significant predictors of fluoropyrimidine toxicity
resolves10.1038/sj.bjc.6605595
Oxaliplatin, irinotecan and capecitabine as first-line therapy in metastatic colorectal cancer (mCRC): a dose-finding study and pharmacogenomic analysis
resolves10.1038/nrg3352
Cancer pharmacogenomics: strategies and challenges
resolves10.2217/pgs.10.167
5-Fluorouracil Pharmacogenomics: Still Rocking after all these years?
resolves10.1016/S1470-2045(15)00286-7
Clinical relevance of DPYD variants c.1679T&gt;G, c.1236G&gt;A/HapB3, and c.1601G&gt;A as predictors of severe fluoropyrimidine-associated toxicity: a systematic review and meta-analysis of individual patient data
resolves10.1038/nrg1916
A tutorial on statistical methods for population association studies
resolves10.1200/JCO.2016.66.6057
Fluorouracil and Dihydropyrimidine Dehydrogenase Genotyping
resolves10.1007/s00280-010-1282-4
DPD-based adaptive dosing of 5-FU in patients with head and neck cancer: impact on treatment efficacy and toxicity
resolves10.1016/j.ygyno.2006.09.002
Phase II clinical trial of capecitabine in the treatment of advanced, persistent or recurrent squamous cell carcinoma of the cervix with translational research: A gynecologic oncology group study
resolves10.1093/annonc/mdp336
EGF61A&gt;G polymorphism as predictive marker of clinical outcome to first-line capecitabine and oxaliplatin in metastatic colorectal cancer
resolves10.1158/1078-0432.1226.11.3
UGT1A7 and UGT1A9 Polymorphisms Predict Response and Toxicity in Colorectal Cancer Patients Treated with Capecitabine/Irinotecan
The 5 references without a DOI — listed, not checked
no DOI — not checkedImmunological quantitation of thymidylate synthase using the monoclonal antibody TS 106 in 5-fluorouracil-sensitive and -resistant human cancer cell lines
no DOI — not checkedA candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS
no DOI — not checkedPolymorphisms in the thymidylate synthase and dihydropyrimidine dehydrogenase genes predict response and toxicity to capecitabine-raltitrexed in colorectal cancer
no DOI — not checkedReply to T. Magnes et al.
no DOI — not checkedPharmacogenetic approach for capecitabine or 5-fluorouracil selection to be combined with oxaliplatin as first-line chemotherapy in advanced colorectal cancer
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