Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pone.0134102
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dc.title | Association of ABCB1 and FLT3 polymorphisms with toxicities and survival in asian patients receiving sunitinib for renal cell carcinoma | |
dc.contributor.author | Chu Y.-H. | |
dc.contributor.author | Li H. | |
dc.contributor.author | Tan H.S. | |
dc.contributor.author | Koh V. | |
dc.contributor.author | Lai J. | |
dc.contributor.author | Phyo W.M. | |
dc.contributor.author | Choudhury Y. | |
dc.contributor.author | Kanesvaran R. | |
dc.contributor.author | Chau N.M. | |
dc.contributor.author | Toh C.K. | |
dc.contributor.author | Ng Q.S. | |
dc.contributor.author | Tan P.H. | |
dc.contributor.author | Chowbay B. | |
dc.contributor.author | Tan M.-H. | |
dc.date.accessioned | 2019-11-06T01:27:56Z | |
dc.date.available | 2019-11-06T01:27:56Z | |
dc.date.issued | 2015 | |
dc.identifier.citation | Chu 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.issn | 19326203 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/161494 | |
dc.description.abstract | Sunitinib 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.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20191101 | |
dc.subject | BIM protein | |
dc.subject | breast cancer resistance protein | |
dc.subject | CD135 antigen | |
dc.subject | multidrug resistance protein 1 | |
dc.subject | sunitinib | |
dc.subject | tumor marker | |
dc.subject | vasculotropin receptor 2 | |
dc.subject | ABCB1 protein, human | |
dc.subject | antineoplastic agent | |
dc.subject | CD135 antigen | |
dc.subject | FLT3 protein, human | |
dc.subject | indole derivative | |
dc.subject | multidrug resistance protein | |
dc.subject | pyrrole derivative | |
dc.subject | sunitinib | |
dc.subject | ABCB1 gene | |
dc.subject | ABCG2 gene | |
dc.subject | adult | |
dc.subject | allele | |
dc.subject | Article | |
dc.subject | Asian | |
dc.subject | BIM gene | |
dc.subject | cancer survival | |
dc.subject | Caucasian | |
dc.subject | comorbidity | |
dc.subject | controlled study | |
dc.subject | drug safety | |
dc.subject | ethnicity | |
dc.subject | female | |
dc.subject | FLT3 gene | |
dc.subject | gene frequency | |
dc.subject | genetic association | |
dc.subject | genetic marker | |
dc.subject | genetic polymorphism | |
dc.subject | hand foot syndrome | |
dc.subject | haplotype | |
dc.subject | human | |
dc.subject | kidney carcinoma | |
dc.subject | leukopenia | |
dc.subject | liver toxicity | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | multiple cycle treatment | |
dc.subject | neutropenia | |
dc.subject | prediction | |
dc.subject | progression free survival | |
dc.subject | thrombocytopenia | |
dc.subject | validation process | |
dc.subject | VEGFR2 gene | |
dc.subject | adolescent | |
dc.subject | adverse drug reaction | |
dc.subject | aged | |
dc.subject | Asian continental ancestry group | |
dc.subject | Carcinoma, Renal Cell | |
dc.subject | disease free survival | |
dc.subject | ethnology | |
dc.subject | genetic predisposition | |
dc.subject | genetics | |
dc.subject | genotype | |
dc.subject | Kidney Neoplasms | |
dc.subject | metastasis | |
dc.subject | middle aged | |
dc.subject | Singapore | |
dc.subject | single nucleotide polymorphism | |
dc.subject | treatment outcome | |
dc.subject | young adult | |
dc.subject | Adolescent | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Antineoplastic Agents | |
dc.subject | Asian Continental Ancestry Group | |
dc.subject | Carcinoma, Renal Cell | |
dc.subject | Disease-Free Survival | |
dc.subject | Drug-Related Side Effects and Adverse Reactions | |
dc.subject | Female | |
dc.subject | fms-Like Tyrosine Kinase 3 | |
dc.subject | Gene Frequency | |
dc.subject | Genetic Predisposition to Disease | |
dc.subject | Genotype | |
dc.subject | Haplotypes | |
dc.subject | Humans | |
dc.subject | Indoles | |
dc.subject | Kidney Neoplasms | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Neoplasm Metastasis | |
dc.subject | P-Glycoproteins | |
dc.subject | Polymorphism, Single Nucleotide | |
dc.subject | Pyrroles | |
dc.subject | Singapore | |
dc.subject | Treatment Outcome | |
dc.subject | Young Adult | |
dc.type | Article | |
dc.contributor.department | DUKE-NUS MEDICAL SCHOOL | |
dc.contributor.department | NUSHS PROJECT | |
dc.description.doi | 10.1371/journal.pone.0134102 | |
dc.description.sourcetitle | PLoS ONE | |
dc.description.volume | 10 | |
dc.description.issue | 8 | |
dc.description.page | e0134102 | |
dc.published.state | Published | |
Appears in Collections: | Staff Publications Elements |
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