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dc.contributor.authorWang, Hsian-Yuen_US
dc.contributor.authorChang, Yu-Lingen_US
dc.contributor.authorCheng, Chun-Chunen_US
dc.contributor.authorChao, Min-Wuen_US
dc.contributor.authorLin, Su-Ien_US
dc.contributor.authorPan, Shiow-Linen_US
dc.contributor.authorHsu, Chih-Chengen_US
dc.contributor.authorLiu, Tsang-Wuen_US
dc.contributor.authorCheng, Han-Chinen_US
dc.contributor.authorTseng, Ching-Pingen_US
dc.contributor.authorLiu, Shih-Jenen_US
dc.contributor.authorTsai, Hui-Juen_US
dc.contributor.authorChang, Hsing-Yien_US
dc.contributor.authorHsu, John T. -A.en_US
dc.date.accessioned2017-04-21T06:56:41Z-
dc.date.available2017-04-21T06:56:41Z-
dc.date.issued2016-12-27en_US
dc.identifier.issn1949-2553en_US
dc.identifier.urihttp://dx.doi.org/10.18632/oncotarget.13185en_US
dc.identifier.urihttp://hdl.handle.net/11536/133073-
dc.description.abstractThe epidermal growth factor receptor (EGFR)-targeting tyrosine kinase inhibitors (TKIs) have shown remarkable benefits in non-small cell lung cancer (NSCLC) patients with drug-sensitive mutations in the EGFR gene. Responsive patients are usually continuously prescribed with TKIs until disease progression. Glucocorticoids (GCs) are potent homeostasis maintaining drugs and are frequently used in cancer patients to alleviate discomforts caused by anti-cancer therapies. Several previous studies reported that concomitant use of GCs may compromise the efficacy of chemo-therapeutics in patients with solid tumors. Little is known in the concomitant use of target therapy with GCs in treating NSCLC. In this study, we hypothesized that concomitant use of GCs in EGFR-TKI therapy may be detrimental and addressed this issue using cell cultures and xenograft studies followed by a retrospective population study based on data from the Taiwan national health insurance system. In cell cultures and xenograft studies, GCs were shown to unequally compromise the anti-cancer efficacy of TKIs in both PC9 and NCI-H1975 NSCLC cells models. In the retrospective population study, patients with similar disease status that were co-medicated with GCs had a significantly higher risk of disease progression.en_US
dc.language.isoen_USen_US
dc.subjectNSCLCen_US
dc.subjectEGFRen_US
dc.subjectTKIen_US
dc.subjectglucocorticoidsen_US
dc.subjectnational health insurance research database taiwanen_US
dc.titleGlucocorticoids may compromise the effect of gefitinib in non-small cell lung canceren_US
dc.identifier.doi10.18632/oncotarget.13185en_US
dc.identifier.journalONCOTARGETen_US
dc.citation.volume7en_US
dc.citation.issue52en_US
dc.citation.spage85917en_US
dc.citation.epage85928en_US
dc.contributor.department生物資訊及系統生物研究所zh_TW
dc.contributor.department分子醫學與生物工程研究所zh_TW
dc.contributor.departmentInstitude of Bioinformatics and Systems Biologyen_US
dc.contributor.departmentInstitute of Molecular Medicine and Bioengineeringen_US
dc.identifier.wosnumberWOS:000391422500022en_US
Appears in Collections:Articles