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Cited 9 time in webofscience Cited 10 time in scopus
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Clinical Significance of ABCG2 Haplotype-tagging Single Nucleotide Polymorphisms in Patients With Unresectable Non-Small Cell Lung Cancer Treated With First-line Platinum-based Chemotherapy

Authors
Kim, Seok-HyunKim, Moon JinCho, Yu JiJeong, Yi YeongKim, Ho-CheolLee, Jong DukHwang, Young SilKim, In-SukLee, SueeOh, Sung YongLing, HuiLee, Gyeong-Won
Issue Date
Jun-2015
Publisher
Lippincott Williams & Wilkins Ltd.
Keywords
non-small cell lung cancer; platinum; ABCG2; drug resistance; survival
Citation
American Journal of Clinical Oncology, v.38, no.3, pp 294 - 299
Pages
6
Indexed
SCI
SCIE
SCOPUS
Journal Title
American Journal of Clinical Oncology
Volume
38
Number
3
Start Page
294
End Page
299
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/17200
DOI
10.1097/COC.0b013e318297f333
ISSN
0277-3732
1537-453X
Abstract
Objectives: The ATP-binding cassette (ABC) ABCG2, involved in multidrug resistance (MDR) in cancer cells, plays an integral role in drug resistance. Single nucleotide polymorphisms (SNPs) have been identified in many MDR-associated ABC genes that seem to influence drug sensitivity/resistance through various mechanisms. Therefore, we investigated whether ABCG2 haplotype-tagging SNPs (htSNPs) were associated with clinical outcomes in patients with unresectable non-small cell lung cancer (NSCLC) treated with front-line platinum-based chemotherapy. Patients and Methods: We genotyped 4 ABCG2 htSNPs for 129 unresectable NSCLC cases treated with first-line platinum-based chemotherapy. Clinical characteristics, treatment outcomes, and predictive value of the htSNPs in patient response, survival, and adverse events related to platinum-based chemotherapy were analyzed according to each ABCG2 htSNP using the chi(2) test, Kaplan-Meier method, and Cox proportional hazard model. Results: The rs2725264 was significantly related to overall survival (OS) (P = 0.018, log-rank test). The median survival duration (in months) for patients with the rs2725264 T/T, T/C, and C/C genotypes was 35.75 (95% confidence interval [CI], 24.25-47.25), 34.25 (hazard ratio [HR] 1.27 [0.68 to 2.35]; 95% CI, 27.16-41.34), and 14.89 (HR 3.22 [1.26 to 8.24], 95% CI, 13.86-15.92), respectively. The rs2725264 was identified as an independent factor by Cox proportional hazard model analysis (P = 0.028). In the taxane-based groups, OS was associated with rs2725264 (P = 0.041), whereas in the gemcitabine-based groups, OS was associated with rs4148149 (P = 0.014). Conclusions: Our data suggest ABCG2 htSNPs rs2725264 (overall group and taxane-platinum combination group) and rs4148149 (gemcitabine- platinum combination group) were associated with OS in unresectable NSCLC patients treated with first-line platinum-based chemotherapy. Thus, the ABCG2 htSNP rs2725264 may be independently associated with OS in unresectable NSCLC patients treated with first-line platinum-based chemotherapy.
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