Cited 10 times in
Temsirolimus in Asian Metastatic/Recurrent Non-clear Cell Renal Carcinoma
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 강버들 | - |
dc.contributor.author | 남정모 | - |
dc.contributor.author | 라선영 | - |
dc.contributor.author | 정현철 | - |
dc.contributor.author | 조남훈 | - |
dc.contributor.author | 이기쁨 | - |
dc.date.accessioned | 2019-12-18T00:30:06Z | - |
dc.date.available | 2019-12-18T00:30:06Z | - |
dc.date.issued | 2019 | - |
dc.identifier.issn | 1598-2998 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/173081 | - |
dc.description.abstract | PURPOSE: Temsirolimus is effective in the treatment for metastatic non-clear cell renal cell carcinoma (nccRCC) with poor prognosis. We aim to investigate the efficacy and tolerability of temsirolimus in treatment of naïve Asian patients with metastatic/recurrent nccRCC. Materials and Methods: From January 2008 to July 2017, data of treatment-naïve, metastatic/recurrent nccRCC patients, who were treated with temsirolimus according to the standard protocol, were collected. The primary end-point was progression-free survival (PFS). Secondary end points were overall survival (OS), objective response rate (ORR), and tolerability of temsirolimus. RESULTS: Forty-four metastatic/recurrent nccRCC patients, 10 from prospective and 34 from retrospective groups, were enrolled; 24 patients (54%) were papillary type, and other histology subtypes included 11 chromophobes (25%), two collecting ducts (5%), one Xp11.2 translocation (2%), and six others (14%). The median PFS and OS were 7.6 months and 17.6 months, res-pectively. ORR was 11% and disease control rate was 83%. Patients with prior nephrectomy had longer PFS (hazard ratio [HR], 0.16; 95% confidence interval [CI], 0.06 to 0.42; p < 0.001) and OS (HR, 0.15; 95% CI, 0.05 to 0.45; p < 0.001). Compared to favorable/intermediate prognosis group, poor prognosis group had shorter median PFS (4.7 months vs. 7.6 months [HR, 2.91; 95% CI, 1.39 to 6.12; p=0.005]) and median OS (9.2 months vs. 17.6 months [HR, 2.84; 95% CI, 1.23 to 6.56; p=0.015]). CONCLUSION: Temsirolimus not only benefits poor-risk nccRCC patients, but it is also effective in favorable or intermediate-risk group in Asians. Temsirolimus was well-tolerated with manageable adverse events. | - |
dc.description.statementOfResponsibility | open | - |
dc.format | application/pdf | - |
dc.language | English, Korean | - |
dc.publisher | Official journal of Korean Cancer Association | - |
dc.relation.isPartOf | CANCER RESEARCH AND TREATMENT | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.title | Temsirolimus in Asian Metastatic/Recurrent Non-clear Cell Renal Carcinoma | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.googleauthor | Jii Bum Lee | - |
dc.contributor.googleauthor | Hyung Soon Park | - |
dc.contributor.googleauthor | Sejung Park | - |
dc.contributor.googleauthor | Hyo Jin Lee | - |
dc.contributor.googleauthor | Kyung A Kwon | - |
dc.contributor.googleauthor | Young Jin Choi | - |
dc.contributor.googleauthor | Yu Jung Kim | - |
dc.contributor.googleauthor | Chung Mo Nam | - |
dc.contributor.googleauthor | Nam Hoon Cho | - |
dc.contributor.googleauthor | Beodeul Kang | - |
dc.contributor.googleauthor | Hyun Cheol Chung | - |
dc.contributor.googleauthor | Sun Young Rha | - |
dc.identifier.doi | 10.4143/crt.2018.671 | - |
dc.contributor.localId | A00029 | - |
dc.contributor.localId | A01264 | - |
dc.contributor.localId | A01316 | - |
dc.contributor.localId | A03773 | - |
dc.contributor.localId | A03812 | - |
dc.relation.journalcode | J00453 | - |
dc.identifier.eissn | 2005-9256 | - |
dc.identifier.pmid | 30999721 | - |
dc.subject.keyword | Asian | - |
dc.subject.keyword | Efficacy | - |
dc.subject.keyword | First-line | - |
dc.subject.keyword | Renal cell carcinoma | - |
dc.subject.keyword | Temsirolimus | - |
dc.subject.keyword | Tolerability | - |
dc.contributor.alternativeName | Kang, Beo Deul | - |
dc.contributor.affiliatedAuthor | 강버들 | - |
dc.contributor.affiliatedAuthor | 남정모 | - |
dc.contributor.affiliatedAuthor | 라선영 | - |
dc.contributor.affiliatedAuthor | 정현철 | - |
dc.contributor.affiliatedAuthor | 조남훈 | - |
dc.citation.volume | 51 | - |
dc.citation.number | 4 | - |
dc.citation.startPage | 1578 | - |
dc.citation.endPage | 1588 | - |
dc.identifier.bibliographicCitation | CANCER RESEARCH AND TREATMENT, Vol.51(4) : 1578-1588, 2019 | - |
dc.identifier.rimsid | 63191 | - |
dc.type.rims | ART | - |
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