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Vandetanib in pretreated patients with advanced non-small cell lung cancer-harboring RET rearrangement: a phase II clinical trial

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dc.contributor.authorLee, Se-Hoon-
dc.contributor.authorLee, J. -K.-
dc.contributor.authorAhn, M. -J.-
dc.contributor.authorKim, D. -W.-
dc.contributor.authorSun, J. -M.-
dc.contributor.authorKeam, B.-
dc.contributor.authorKim, T. M.-
dc.contributor.authorHeo, D. S.-
dc.contributor.authorAhn, J. S.-
dc.contributor.authorChoi, Y. -L.-
dc.contributor.authorMin, H. -S.-
dc.contributor.authorJeon, Y. K.-
dc.contributor.authorPark, K.-
dc.date.accessioned2020-04-27T11:05:57Z-
dc.date.available2020-04-27T11:05:57Z-
dc.date.created2018-07-26-
dc.date.issued2017-02-
dc.identifier.citationAnnals of Oncology, Vol.28 No.2, pp.292-297-
dc.identifier.issn0923-7534-
dc.identifier.other41332-
dc.identifier.urihttps://hdl.handle.net/10371/165246-
dc.description.abstractBackground: Chromosomal rearrangements involving RET, which are found in about 1% of non-small cell lung cancer (NSCLC), define a unique molecular subset. We performed this study to examine the efficacy and safety of vandetanib 300 mg daily in this patient population. Patients and methods: This study was a multi-center, open-label, phase II clinical trial. Patients were enrolled if they had metastatic or recurrent NSCLC with a RET rearrangement, which was confirmed by fluorescence in situ hybridization, had progressive disease against platinum-based doublet chemotherapy, and had a performance status of 0-2. The primary endpoint was the objective response rate. Results: A total of 18 patients were enrolled in this study between July 2013 and October 2015. Patients were aged 35-71 years; three had a performance status of 2, and the majority were a heavily pretreated population (two different previous chemotherapy regimens in 72% of the patients). Among the 17 evaluable patients, three had a partial response (objective response rate >= 18%) and eight had a stable disease (disease control rate = 65%). Among these patients, the partial response or disease stabilization was durable for more than 6 months in eight patients. Vandetanib also showed a progression-free survival of 4.5 months, and an overall survival of 11.6 months during a median follow-up duration of 14 months. The safety profile was comparable with previous studies of vandetanib. Most vandetanib-related adverse events were mild with prevalent hypertension and rash (in>70% of patients). Grade 3 toxicity included hypertension (n = 3), QT prolongation (2), and elevation of aminotransferases (1), and as a consequence the dose was reduced in four patients. There were no adverse events associated with grade 4 or 5 toxicity. Conclusion: Vandetanib is moderately active in pretreated patients with advanced NSCLC-harboring RET rearrangements.-
dc.language영어-
dc.publisherOxford University Press-
dc.titleVandetanib in pretreated patients with advanced non-small cell lung cancer-harboring RET rearrangement: a phase II clinical trial-
dc.typeArticle-
dc.contributor.AlternativeAuthor전윤경-
dc.contributor.AlternativeAuthor김동완-
dc.identifier.doi10.1093/annonc/mdw559-
dc.citation.journaltitleAnnals of Oncology-
dc.identifier.wosid000397278300015-
dc.identifier.scopusid2-s2.0-85019621936-
dc.citation.endpage297-
dc.citation.number2-
dc.citation.startpage292-
dc.citation.volume28-
dc.identifier.sci000397278300015-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, D. -W.-
dc.contributor.affiliatedAuthorJeon, Y. K.-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusTHYROID-CANCER-
dc.subject.keywordPlusADENOCARCINOMA-
dc.subject.keywordPlusFUSION-
dc.subject.keywordPlusALK-
dc.subject.keywordPlusKINASE-
dc.subject.keywordPlusCRIZOTINIB-
dc.subject.keywordPlusMEDULLARY-
dc.subject.keywordPlusINHIBITOR-
dc.subject.keywordAuthorvandetanib-
dc.subject.keywordAuthorRET rearrangement-
dc.subject.keywordAuthornon-small cell lung cancer-
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