Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0134102
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dc.titleAssociation of ABCB1 and FLT3 polymorphisms with toxicities and survival in asian patients receiving sunitinib for renal cell carcinoma
dc.contributor.authorChu Y.-H.
dc.contributor.authorLi H.
dc.contributor.authorTan H.S.
dc.contributor.authorKoh V.
dc.contributor.authorLai J.
dc.contributor.authorPhyo W.M.
dc.contributor.authorChoudhury Y.
dc.contributor.authorKanesvaran R.
dc.contributor.authorChau N.M.
dc.contributor.authorToh C.K.
dc.contributor.authorNg Q.S.
dc.contributor.authorTan P.H.
dc.contributor.authorChowbay B.
dc.contributor.authorTan M.-H.
dc.date.accessioned2019-11-06T01:27:56Z
dc.date.available2019-11-06T01:27:56Z
dc.date.issued2015
dc.identifier.citationChu Y.-H., Li H., Tan H.S., Koh V., Lai J., Phyo W.M., Choudhury Y., Kanesvaran R., Chau N.M., Toh C.K., Ng Q.S., Tan P.H., Chowbay B., Tan M.-H. (2015). Association of ABCB1 and FLT3 polymorphisms with toxicities and survival in asian patients receiving sunitinib for renal cell carcinoma. PLoS ONE 10 (8) : e0134102. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0134102
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161494
dc.description.abstractSunitinib is a tyrosine kinase inhibitor used as first-line treatment for metastatic renal cell carcinoma (mRCC). Asian ethnicity has been previously associated with lower clearance and greater toxicities for sunitinib treatment, relative to Caucasian ethnicity. Research focusing on identifying corresponding biomarkers of efficacy and toxicity has been hitherto conducted in Caucasian populations, and few of the reported associations have been externally validated. Our work thus aims to investigate candidate biomarkers in Asian patients receiving sunitinib, comparing the observed genotype effects with those reported in Caucasian populations. Using data from 97 Asian mRCC patients treated with sunitinib, we correlated 7 polymorphisms in FLT3, ABCB1, VEGFR2, ABCG2 and BIMwith patient toxicities, response, and survival. We observed a stronger association of FLT3 738T genotype with leucopenia in our Asian dataset than that previously reported in Caucasian mRCC patients (odds ratio [OR] =8.0; P=0.03). We observed significant associations of FLT3 738T (OR=2.7), ABCB11236T (OR=0.3), ABCB1 3435T (OR=0.1), ABCB1 2677T (OR=0.4), ABCG2 421A (OR=0.3) alleles and ABCB1 3435, 1236, 2677 TTT haplotype (OR=0.1) on neutropenia. Primary resistance (OR=0.1, P=0.004) and inferior survival (progression-free: hazard ratio [HR]=5.5, P=0.001; overall: HR=5.0, P=0.005) were associated with the ABCB1 3435, 1236, 2677 TTT haplotype. In conclusion, ABCB1 and FLT3 polymorphisms may be helpful in predicting sunitinib toxicities, response and survival benefit in Asian mRCC patients. We have also validated the association between FLT3 738T and sunitinib-induced leucopenia previously reported in Caucasian populations, but have not validated other reported genetic associations. © 2015 Chu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectBIM protein
dc.subjectbreast cancer resistance protein
dc.subjectCD135 antigen
dc.subjectmultidrug resistance protein 1
dc.subjectsunitinib
dc.subjecttumor marker
dc.subjectvasculotropin receptor 2
dc.subjectABCB1 protein, human
dc.subjectantineoplastic agent
dc.subjectCD135 antigen
dc.subjectFLT3 protein, human
dc.subjectindole derivative
dc.subjectmultidrug resistance protein
dc.subjectpyrrole derivative
dc.subjectsunitinib
dc.subjectABCB1 gene
dc.subjectABCG2 gene
dc.subjectadult
dc.subjectallele
dc.subjectArticle
dc.subjectAsian
dc.subjectBIM gene
dc.subjectcancer survival
dc.subjectCaucasian
dc.subjectcomorbidity
dc.subjectcontrolled study
dc.subjectdrug safety
dc.subjectethnicity
dc.subjectfemale
dc.subjectFLT3 gene
dc.subjectgene frequency
dc.subjectgenetic association
dc.subjectgenetic marker
dc.subjectgenetic polymorphism
dc.subjecthand foot syndrome
dc.subjecthaplotype
dc.subjecthuman
dc.subjectkidney carcinoma
dc.subjectleukopenia
dc.subjectliver toxicity
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectmultiple cycle treatment
dc.subjectneutropenia
dc.subjectprediction
dc.subjectprogression free survival
dc.subjectthrombocytopenia
dc.subjectvalidation process
dc.subjectVEGFR2 gene
dc.subjectadolescent
dc.subjectadverse drug reaction
dc.subjectaged
dc.subjectAsian continental ancestry group
dc.subjectCarcinoma, Renal Cell
dc.subjectdisease free survival
dc.subjectethnology
dc.subjectgenetic predisposition
dc.subjectgenetics
dc.subjectgenotype
dc.subjectKidney Neoplasms
dc.subjectmetastasis
dc.subjectmiddle aged
dc.subjectSingapore
dc.subjectsingle nucleotide polymorphism
dc.subjecttreatment outcome
dc.subjectyoung adult
dc.subjectAdolescent
dc.subjectAdult
dc.subjectAged
dc.subjectAntineoplastic Agents
dc.subjectAsian Continental Ancestry Group
dc.subjectCarcinoma, Renal Cell
dc.subjectDisease-Free Survival
dc.subjectDrug-Related Side Effects and Adverse Reactions
dc.subjectFemale
dc.subjectfms-Like Tyrosine Kinase 3
dc.subjectGene Frequency
dc.subjectGenetic Predisposition to Disease
dc.subjectGenotype
dc.subjectHaplotypes
dc.subjectHumans
dc.subjectIndoles
dc.subjectKidney Neoplasms
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNeoplasm Metastasis
dc.subjectP-Glycoproteins
dc.subjectPolymorphism, Single Nucleotide
dc.subjectPyrroles
dc.subjectSingapore
dc.subjectTreatment Outcome
dc.subjectYoung Adult
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.contributor.departmentNUSHS PROJECT
dc.description.doi10.1371/journal.pone.0134102
dc.description.sourcetitlePLoS ONE
dc.description.volume10
dc.description.issue8
dc.description.pagee0134102
dc.published.statePublished
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