Cited 6 times in
The prognostic effect of prostate-specific antigen half-life at the first follow-up visit in newly diagnosed metastatic prostate cancer
DC Field | Value | Language |
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dc.contributor.author | 나군호 | - |
dc.contributor.author | 최영득 | - |
dc.contributor.author | 한경석 | - |
dc.contributor.author | 홍성준 | - |
dc.contributor.author | 구교철 | - |
dc.contributor.author | 김기홍 | - |
dc.contributor.author | 김대근 | - |
dc.date.accessioned | 2016-02-04T11:48:06Z | - |
dc.date.available | 2016-02-04T11:48:06Z | - |
dc.date.issued | 2015 | - |
dc.identifier.issn | 1078-1439 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/141233 | - |
dc.description.abstract | PURPOSE: Several prostate-specific antigen (PSA) kinetics parameters such as nadir PSA level and time to nadir PSA level are used commonly as predictive prognostic factors for patients with metastatic prostate cancer (mPCa) who have undergone androgen deprivation therapy. However, based on the limitations of these factors, earlier and more clinically available prognostic factors are needed. Therefore, we examined the PSA half-life (PSAHL) estimated at the first follow-up visit as a prognostic factor of newly diagnosed mPCa. METHODS: We performed a retrospective review of 309 patients with newly diagnosed mPCa who had undergone androgen deprivation therapy. After categorizing the included patients to short and long PSAHL groups, based on the median PSAHL value, Cox regression analyses were performed to identify independent prognostic factors of newly diagnosed mPCa. The Kaplan-Meier method was used for detecting differences in survival between both the groups. RESULTS: The median follow-up period was 44 months, and the prostate cancer-specific mortality (PCSM)-free survival length was 65 months in all included patients. Long PSAHL group (hazard ratio [HR] = 2.383, P<0.001), nadir PSA level (HR = 1.004, P<0.001), time to nadir PSA level (HR = 0.856; P<0.001), and Gleason score 8 to 10 relative to 6 to 7 (HR = 2.025; P = 0.008) were found to be independent predictors of the PCSM. By the Kaplan-Meier method, the median PCSM-free survival of the short PSAHL group was 73.7 (95% CI: 54.8-92.6) and of the long PSAHL group was 52.5 months (95% CI: 33.4-71.6). This difference between both the groups was found to be statistically significant (P = 0.014, log rank test). CONCLUSIONS: PSAHL estimated at the first follow-up visit is an independent prognostic factor for newly diagnosed mPCa. If the prospective validation test is performed on a large scale, it may demonstrate that PSAHL is an early surrogate prognostic factor of newly diagnosed mPCa. | - |
dc.description.statementOfResponsibility | open | - |
dc.relation.isPartOf | UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Biomarkers, Tumor/blood | - |
dc.subject.MESH | Disease-Free Survival | - |
dc.subject.MESH | Half-Life | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Kaplan-Meier Estimate | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Proportional Hazards Models | - |
dc.subject.MESH | Prostate-Specific Antigen/blood* | - |
dc.subject.MESH | Prostatic Neoplasms/blood* | - |
dc.subject.MESH | Prostatic Neoplasms/mortality | - |
dc.subject.MESH | Retrospective Studies | - |
dc.title | The prognostic effect of prostate-specific antigen half-life at the first follow-up visit in newly diagnosed metastatic prostate cancer | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Urology (비뇨기과학) | - |
dc.contributor.googleauthor | Ki Hong Kim | - |
dc.contributor.googleauthor | Kyung Seok Han | - |
dc.contributor.googleauthor | Kwang Hyun Kim | - |
dc.contributor.googleauthor | Dae Keun Kim | - |
dc.contributor.googleauthor | Kyo Chul Koo | - |
dc.contributor.googleauthor | Koon Ho Rha | - |
dc.contributor.googleauthor | Young Deuk Choi | - |
dc.contributor.googleauthor | Sung Joon Hong | - |
dc.identifier.doi | 10.1016/j.urolonc.2015.04.007 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A01227 | - |
dc.contributor.localId | A04111 | - |
dc.contributor.localId | A04264 | - |
dc.contributor.localId | A04402 | - |
dc.contributor.localId | A00188 | - |
dc.contributor.localId | A00343 | - |
dc.contributor.localId | A00365 | - |
dc.relation.journalcode | J02774 | - |
dc.identifier.eissn | 1873-2496 | - |
dc.identifier.pmid | 26004165 | - |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S107814391500157X | - |
dc.subject.keyword | Androgen deprivation therapy | - |
dc.subject.keyword | Metastasis | - |
dc.subject.keyword | Prostate cancer | - |
dc.subject.keyword | Prostate-specific antigen | - |
dc.contributor.alternativeName | Rha, Koon Ho | - |
dc.contributor.alternativeName | Choi, Young Deuk | - |
dc.contributor.alternativeName | Han, Kyung Seok | - |
dc.contributor.alternativeName | Hong, Sung Joon | - |
dc.contributor.alternativeName | Koo, Kyo Chul | - |
dc.contributor.alternativeName | Kim, Ki Hong | - |
dc.contributor.alternativeName | Kim, Dae Keun | - |
dc.contributor.affiliatedAuthor | Rha, Koon Ho | - |
dc.contributor.affiliatedAuthor | Choi, Young Deuk | - |
dc.contributor.affiliatedAuthor | Han, Kyung Seok | - |
dc.contributor.affiliatedAuthor | Hong, Sung Joon | - |
dc.contributor.affiliatedAuthor | Koo, Kyo Chul | - |
dc.contributor.affiliatedAuthor | Kim, Ki Hong | - |
dc.contributor.affiliatedAuthor | Kim, Dae Keun | - |
dc.rights.accessRights | not free | - |
dc.citation.volume | 33 | - |
dc.citation.number | 9 | - |
dc.citation.startPage | 383.e17 | - |
dc.citation.endPage | 383.e22 | - |
dc.identifier.bibliographicCitation | UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, Vol.33(9) : 383.e17-383.e22, 2015 | - |
dc.identifier.rimsid | 31426 | - |
dc.type.rims | ART | - |
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