An internally and externally validated nomogram for predicting the risk of irinotecan-induced severe neutropenia in advanced colorectal cancer patients

scientific article published on 16 April 2015

An internally and externally validated nomogram for predicting the risk of irinotecan-induced severe neutropenia in advanced colorectal cancer patients is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1038/BJC.2015.122
P932PMC publication ID4430714
P698PubMed publication ID25880011
P5875ResearchGate publication ID275051704

P2093author name stringM Nakamura
T Takahashi
A Tsuji
S Sadahiro
Yukio Ando
Y Ohashi
C Tanaka
K Fujita
T Sugiyama
M Sugihara
K Uehara
K Shinozaki
Y Sakata
S Morita
T Moriwaki
W Ichikawa
Y Takii
H Miyauchi
Y Okutani
K Minamimura
P2860cites workPhase II study of CPT-11, a new camptothecin derivative, in metastatic colorectal cancer. CPT-11 Gastrointestinal Cancer Study Group.Q54241012
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Irinotecan pharmacokinetics/pharmacodynamics and UGT1A genetic polymorphisms in Japanese: roles of UGT1A1*6 and *28Q80452767
UGT1A1*28 genotype and irinotecan-induced neutropenia: dose mattersQ80865711
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Comprehensive analysis of UGT1A polymorphisms predictive for pharmacokinetics and treatment outcome in patients with non-small-cell lung cancer treated with irinotecan and cisplatinQ83195720
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UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancerQ24648015
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Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecanQ28249001
Risk factors for severe adverse effects and treatment-related deaths in Japanese patients treated with irinotecan-based chemotherapy: a postmarketing surveyQ33406703
Dose-finding and pharmacokinetic study to optimize the dosing of irinotecan according to the UGT1A1 genotype of patients with cancerQ33927990
Pharmacogenetic predictors of adverse events and response to chemotherapy in metastatic colorectal cancer: results from North American Gastrointestinal Intergroup Trial N9741.Q33990876
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Dose-response and trend analysis in epidemiology: alternatives to categorical analysisQ34294668
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A genotype-directed phase I-IV dose-finding study of irinotecan in combination with fluorouracil/leucovorin as first-line treatment in advanced colorectal cancerQ35108413
Genotype-driven phase I study of irinotecan administered in combination with fluorouracil/leucovorin in patients with metastatic colorectal cancerQ36915163
Clinical and pharmacogenetic factors associated with irinotecan toxicityQ37192912
Can UGT1A1 genotyping reduce morbidity and mortality in patients with metastatic colorectal cancer treated with irinotecan? An evidence-based reviewQ37345974
Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomesQ37378223
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UGT1A1*28 polymorphism predicts irinotecan-induced severe toxicities without affecting treatment outcome and survival in patients with metastatic colorectal carcinomaQ40426198
Irinotecan plus S-1 (IRIS) versus fluorouracil and folinic acid plus irinotecan (FOLFIRI) as second-line chemotherapy for metastatic colorectal cancer: a randomised phase 2/3 non-inferiority study (FIRIS study).Q42937632
Additive effects of drug transporter genetic polymorphisms on irinotecan pharmacokinetics/pharmacodynamics in Japanese cancer patientsQ43273259
UGT1A1*6, 1A7*3, and 1A9*22 genotypes predict severe neutropenia in FOLFIRI-treated metastatic colorectal cancer in two prospective studies in Japan.Q43714693
Identification and activities of human carboxylesterases for the activation of CPT-11, a clinically approved anticancer drugQ43804754
Human carboxylesterase 2 is commonly expressed in tumor tissue and is correlated with activation of irinotecanQ44097380
UGT1A1 haplotypes associated with reduced glucuronidation and increased serum bilirubin in irinotecan-administered Japanese patients with cancerQ44922991
Relevance of different UGT1A1 polymorphisms in irinotecan-induced toxicity: a molecular and clinical study of 75 patientsQ45009159
UGT1A7 and UGT1A9 polymorphisms predict response and toxicity in colorectal cancer patients treated with capecitabine/irinotecanQ45263765
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue10
P407language of work or nameEnglishQ1860
P921main subjectcolorectal cancerQ188874
P304page(s)1709-1716
P577publication date2015-04-16
P1433published inBritish Journal of CancerQ326309
P1476titleAn internally and externally validated nomogram for predicting the risk of irinotecan-induced severe neutropenia in advanced colorectal cancer patients
P478volume112

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cites work (P2860)
Q88813314Association of Patient Sex With Chemotherapy-Related Toxic Effects: A Retrospective Analysis of the PETACC-3 Trial Conducted by the EORTC Gastrointestinal Group
Q88651638Chemotherapy-Induced Neutropenia as a Prognostic and Predictive Marker of Outcomes in Solid-Tumor Patients
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Q93186317Impact of UGT1A1 genetic polymorphism on toxicity in unresectable pancreatic cancer patients undergoing FOLFIRINOX
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Q93143934Patient factors and their impact on neutropenic events: a systematic review and meta-analysis
Q59797795Severe Neutropenia is Associated with Better Clinical Outcomes in Patients with Advanced Pancreatic Cancer Who Receive Modified FOLFIRINOX Therapy
Q26778004Treatment-related gastrointestinal toxicities and advanced colorectal or pancreatic cancer: A critical update
Q37682812UGT1A1 polymorphisms in cancer: impact on irinotecan treatment

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