DPYD genotype-guided fluoropyrimidines dose: is it ready for prime time?
暂无分享,去创建一个
[1] J. Schellens,et al. DPYD genotype-guided dose individualization to improve patient safety of fluoropyrimidine therapy: call for a drug label update , 2017, Annals of oncology : official journal of the European Society for Medical Oncology.
[2] M. Martín,et al. Pharmacogenetic clinical randomized phase II trial to evaluate the efficacy and safety of FOLFIRI with high dose of irinotecan (FOLFIRI-HD) in metastatic colorectal cancer patients according to UGT1A 1 genotype. , 2017, Annals of oncology : official journal of the European Society for Medical Oncology.
[3] F. Pinguet,et al. New advances in DPYD genotype and risk of severe toxicity under capecitabine , 2017, PloS one.
[4] J. Schellens,et al. Improving safety of fluoropyrimidine chemotherapy by individualizing treatment based on dihydropyrimidine dehydrogenase activity - Ready for clinical practice? , 2016, Cancer treatment reviews.
[5] R. Greil,et al. Fluorouracil and Dihydropyrimidine Dehydrogenase Genotyping. , 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[6] J. Schellens,et al. Upfront Genotyping of DPYD*2A to Individualize Fluoropyrimidine Therapy: A Safety and Cost Analysis. , 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[7] F. Innocenti,et al. Genotype-Guided Dosing Study of FOLFIRI plus Bevacizumab in Patients with Metastatic Colorectal Cancer , 2016, Clinical Cancer Research.
[8] U. Amstutz,et al. Rs895819 in MIR27A improves the predictive value of DPYD variants to identify patients at risk of severe fluoropyrimidine‐associated toxicity , 2016, International journal of cancer.
[9] J. Schellens,et al. Reply to T. Magnes et al. , 2016, Journal of Clinical Oncology.
[10] R. Diasio,et al. Is It Finally Time for a Personalized Medicine Approach for Fluorouracil-Based Therapies? , 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[11] J. Ciccolini. DPD deficiency in patients treated with fluorouracil. , 2015, The Lancet. Oncology.
[12] J. Sanderson,et al. Clinical relevance of DPYD variants c.1679T>G, c.1236G>A/HapB3, and c.1601G>A as predictors of severe fluoropyrimidine-associated toxicity: a systematic review and meta-analysis of individual patient data. , 2015, The Lancet. Oncology.
[13] Gabriel L. Butterfield,et al. Comparative functional analysis of DPYD variants of potential clinical relevance to dihydropyrimidine dehydrogenase activity. , 2014, Cancer research.
[14] J. Maring,et al. Evaluation of predictive tests for screening for dihydropyrimidine dehydrogenase deficiency , 2014, The Pharmacogenomics Journal.
[15] Teri E. Klein,et al. Clinical Pharmacogenetics Implementation Consortium Guidelines for Dihydropyrimidine Dehydrogenase Genotype and Fluoropyrimidine Dosing , 2013, Clinical pharmacology and therapeutics.
[16] R. Danesi,et al. DPYD IVS14+1G>A and 2846A>T genotyping for the prediction of severe fluoropyrimidine-related toxicity: a meta-analysis. , 2013, Pharmacogenomics.
[17] M. Baiget,et al. A genotype-directed phase I–IV dose-finding study of irinotecan in combination with fluorouracil/leucovorin as first-line treatment in advanced colorectal cancer , 2011, British Journal of Cancer.
[18] R. Diasio,et al. Dihydropyrimidine dehydrogenase deficiency, a pharmacogenetic syndrome associated with potentially life-threatening toxicity following 5-fluorouracil administration. , 2004, Clinical colorectal cancer.
[19] Soma Das,et al. Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.