367 423

Cited 200 times in

Impact of bone and liver metastases on patients with renal cell carcinoma treated with targeted therapy.

DC Field Value Language
dc.contributor.author라선영-
dc.date.accessioned2015-12-28T11:04:54Z-
dc.date.available2015-12-28T11:04:54Z-
dc.date.issued2014-
dc.identifier.issn0302-2838-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/138652-
dc.description.abstractBACKGROUND: The skeleton and liver are frequently involved sites of metastasis in patients with metastatic renal cell carcinoma (RCC). OBJECTIVE: To analyze outcomes based on the presence of bone metastases (BMs) and/or liver metastases (LMs) in patients with RCC treated with targeted therapy. DESIGN, SETTING, AND PARTICIPANTS: We conducted a review from the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) of 2027 patients with metastatic RCC. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: We analyzed the impact of the site of metastasis on overall survival (OS) and time-to-treatment failure. Statistical analyses were performed using multivariable Cox regression. RESULTS AND LIMITATIONS: The presence of BMs was 34% overall, and when stratified by IMDC risk groups was 27%, 33%, and 43% in the favorable-, intermediate-, and poor-risk groups, respectively (p<0.001). The presence of LMs was 19% overall and higher in the poor-risk patients (23%) compared with the favorable- or intermediate-risk groups (17%) (p=0.003). When patients were classified into four groups based on the presence of BMs and/or LMs, the hazard ratio, adjusted for IMDC risk factors, was 1.4 (95% confidence interval [CI], 1.22-1.62) for BMs, 1.42 (95% CI, 1.17-1.73) for LMs, and 1.82 (95% CI, 1.47-2.26) for both BMs and LMs compared with other metastatic sites (p<0.0001). The prediction model performance for OS was significantly improved when BMs and LMs were added to the IMDC prognostic model (likelihood ratio test p<0.0001). Data in this analysis were collected retrospectively. CONCLUSIONS: The presence of BMs and LMs in patients treated with targeted agents has a negative impact on survival. Patients with BMs and/or LMs may benefit from earlier inclusion on clinical trials of novel agents or combination-based therapies.-
dc.description.statementOfResponsibilityopen-
dc.format.extent577~584-
dc.relation.isPartOfEUROPEAN UROLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHBone Neoplasms/secondary*-
dc.subject.MESHCarcinoma, Renal Cell/drug therapy*-
dc.subject.MESHCarcinoma, Renal Cell/secondary*-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHKidney Neoplasms/drug therapy*-
dc.subject.MESHKidney Neoplasms/pathology*-
dc.subject.MESHLiver Neoplasms/secondary*-
dc.subject.MESHMale-
dc.subject.MESHMolecular Targeted Therapy-
dc.subject.MESHRetrospective Studies-
dc.titleImpact of bone and liver metastases on patients with renal cell carcinoma treated with targeted therapy.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorRana R. McKay-
dc.contributor.googleauthorNils Kroeger-
dc.contributor.googleauthorWanling Xie-
dc.contributor.googleauthorJae Lyun Lee-
dc.contributor.googleauthorJennifer J. Knox-
dc.contributor.googleauthorGeorg A. Bjarnason-
dc.contributor.googleauthorMary J. MacKenzie-
dc.contributor.googleauthorLori Wood-
dc.contributor.googleauthorSandy Srinivas-
dc.contributor.googleauthorUlka N. Vaishampayan-
dc.contributor.googleauthorSun Young Rha-
dc.contributor.googleauthorSumanta K. Pal-
dc.contributor.googleauthorFrede Donskov-
dc.contributor.googleauthorSrinivas K. Tantravahi-
dc.contributor.googleauthorBrian I. Rini-
dc.contributor.googleauthorDaniel Y. C. Heng-
dc.contributor.googleauthorToni K. Choueiri-
dc.identifier.doi10.1016/j.eururo.2013.08.012-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01316-
dc.relation.journalcodeJ00854-
dc.identifier.eissn1873-7560-
dc.identifier.pmid23962746-
dc.subject.keywordBone metastases-
dc.subject.keywordLiver metastases-
dc.subject.keywordOutcome-
dc.subject.keywordRenal cell carcinoma-
dc.subject.keywordVEGF therapy-
dc.subject.keywordmTOR inhibitors-
dc.contributor.alternativeNameRha, Sun Young-
dc.contributor.affiliatedAuthorRha, Sun Young-
dc.citation.volume65-
dc.citation.number3-
dc.citation.startPage577-
dc.citation.endPage584-
dc.identifier.bibliographicCitationEUROPEAN UROLOGY, Vol.65(3) : 577-584, 2014-
dc.identifier.rimsid38468-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.