dc.contributor.author | Nikitas, N. | en |
dc.contributor.author | Karadimou, A. | en |
dc.contributor.author | Tsitoura, E. | en |
dc.contributor.author | Soupos, N. | en |
dc.contributor.author | Tsiatas, M. | en |
dc.contributor.author | Karavasilis, V. | en |
dc.contributor.author | Pectasides, Dimitrios | en |
dc.contributor.author | Pavlidis, Nicholas | en |
dc.contributor.author | Chrisofos, M. | en |
dc.contributor.author | Adamakis, I. | en |
dc.contributor.author | Murray, S. | en |
dc.contributor.author | Fountzilas, George | en |
dc.contributor.author | Dimopoulos, M. A. | en |
dc.contributor.author | Bamias, A. T. | en |
dc.creator | Nikitas, N. | en |
dc.creator | Karadimou, A. | en |
dc.creator | Tsitoura, E. | en |
dc.creator | Soupos, N. | en |
dc.creator | Tsiatas, M. | en |
dc.creator | Karavasilis, V. | en |
dc.creator | Pectasides, Dimitrios | en |
dc.creator | Pavlidis, Nicholas | en |
dc.creator | Chrisofos, M. | en |
dc.creator | Adamakis, I. | en |
dc.creator | Murray, S. | en |
dc.creator | Fountzilas, George | en |
dc.creator | Dimopoulos, M. A. | en |
dc.creator | Bamias, A. T. | en |
dc.date.accessioned | 2018-06-22T09:54:05Z | |
dc.date.available | 2018-06-22T09:54:05Z | |
dc.date.issued | 2012 | |
dc.identifier.uri | https://gnosis.library.ucy.ac.cy/handle/7/42190 | |
dc.description.abstract | Aim: The association between two polymorphisms of ERCC1 and treatment outcomes after platinum-based chemotherapy in patients with advanced urothelial cancer (UC) was examined. Materials & methods: Genotyping of 19007C>T and 8092C>A polymorphisms was determined by PCR amplification and RFLP in 113 advanced UC patients, treated with platinum-based chemotherapy. Results: Seventy eight patients (69%) were carriers of the 19007T polymorphic allele: 51 (45%) heterozygotes and 27 (24%) homozygotes. Fifty three (47%) patients were carriers of the 8092A polymorphic allele: the frequencies of C/A and A/A genotypes were 37% and 10%, respectively. The T/T genotype was independently associated with prolonged median cancer-specific survival (not-reached vs 14.8 months; p = 0.026). There was no interaction between T/T or any other genotype with the type of platinum derivative (cisplatin/carboplatin). Conclusion: 19007C>T, especially in its homozygotic state, but not 8092C>A polymorphism, could be a useful prognostic marker in advanced UC treated with platinum-based chemotherapy. Original submitted 17 July 2012; Revision submitted 21 September 201. © 2012 Future Medicine Ltd. | en |
dc.language.iso | eng | en |
dc.source | Pharmacogenomics | en |
dc.subject | Article | en |
dc.subject | Cancer chemotherapy | en |
dc.subject | Cisplatin | en |
dc.subject | Doxorubicin | en |
dc.subject | Human | en |
dc.subject | Methotrexate | en |
dc.subject | Vinblastine | en |
dc.subject | Humans | en |
dc.subject | Adult | en |
dc.subject | Aged | en |
dc.subject | Cancer patient | en |
dc.subject | Female | en |
dc.subject | Major clinical study | en |
dc.subject | Middle aged | en |
dc.subject | Advanced cancer | en |
dc.subject | Carboplatin | en |
dc.subject | Drug response | en |
dc.subject | Neoplasm staging | en |
dc.subject | Platinum derivative | en |
dc.subject | Disease-free survival | en |
dc.subject | Gemcitabine | en |
dc.subject | Treatment outcome | en |
dc.subject | Cancer prognosis | en |
dc.subject | Male | en |
dc.subject | Genetic association | en |
dc.subject | Single nucleotide polymorphism | en |
dc.subject | Gene frequency | en |
dc.subject | Genotype | en |
dc.subject | Polymorphism | en |
dc.subject | Single nucleotide | en |
dc.subject | Survival time | en |
dc.subject | Urogenital tract cancer | en |
dc.subject | Kaplan-meier estimate | en |
dc.subject | Dna | en |
dc.subject | Gene amplification | en |
dc.subject | Polymerase chain reaction | en |
dc.subject | Messenger rna | en |
dc.subject | Progression free survival | en |
dc.subject | Dna-binding proteins | en |
dc.subject | Genetic analysis | en |
dc.subject | Heterozygote | en |
dc.subject | Homozygote | en |
dc.subject | Platinum | en |
dc.subject | Urologic neoplasms | en |
dc.subject | Restriction fragment length polymorphism | en |
dc.subject | Biomarkers | en |
dc.subject | Cancer specific survival | en |
dc.subject | Dose densification | en |
dc.subject | Endonucleases | en |
dc.subject | Ercc1 gene | en |
dc.subject | Excision repair cross complementing protein 1 | en |
dc.subject | Genetic association studies | en |
dc.subject | Human ercc1 gene | en |
dc.subject | Nucleotide excision repair | en |
dc.subject | Pharmacogenetics | en |
dc.subject | Pharmacological | en |
dc.subject | Single-nucleotide polymorphism | en |
dc.subject | Urothelial cancer | en |
dc.title | Association of ERCC1 SNPs with outcome in platinum-treated patients with advanced urothelial cancer: A Hellenic Cooperative Oncology Group study | en |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | 10.2217/pgs.12.162 | |
dc.description.volume | 13 | |
dc.description.issue | 14 | |
dc.description.startingpage | 1595 | |
dc.description.endingpage | 1607 | |
dc.author.faculty | Ιατρική Σχολή / Medical School | |
dc.author.department | Ιατρική Σχολή / Medical School | |
dc.type.uhtype | Article | en |
dc.contributor.orcid | Pavlidis, Nicholas [0000-0002-2195-9961] | |
dc.contributor.orcid | Karavasilis, V. [0000-0002-5806-9399] | |
dc.gnosis.orcid | 0000-0002-2195-9961 | |
dc.gnosis.orcid | 0000-0002-5806-9399 | |