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Yonsei Criteria: A New Protocol for Active Surveillance in the Era of Robotic and Local Ablative Surgeries

DC Field Value Language
dc.contributor.author김광현-
dc.contributor.author나군호-
dc.contributor.author신태영-
dc.contributor.author임세이캣-
dc.contributor.author정병하-
dc.contributor.author최영득-
dc.contributor.author홍성준-
dc.date.accessioned2014-12-18T09:37:48Z-
dc.date.available2014-12-18T09:37:48Z-
dc.date.issued2013-
dc.identifier.issn1558-7673-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/88530-
dc.description.abstractBACKGROUND: The objective of this study was to develop a new AS protocol and compare it with the existing selected published AS protocols by examining the pathological characteristics of post-RARP specimens in patients eligible for AS. MATERIALS AND METHODS: From a database of 1046 patients, 344 post-RARP patients with biopsy Gleason scores ≤ 6 prostate cancer (PCa) without neoadjuvant therapy were included. Six AS protocols were identified and evaluated for pathological and oncological end points. Four new AS criteria were proposed and evaluated. The probabilities of each end point were estimated using logistic regression modeling. Areas under the receiver operating curve were calculated for each protocol and end point. RESULTS: Across all the selected protocols, biochemical recurrence occurred in 0 to 1.9% of patients; extracapsular extension (ECE) in 0 to 5.9%; lymph node involvement (LNI) in 0 to 1.3%; and upgrading to Gleason score ≥ 7 in 12.9% to 36.4%. We found that our new AS criteria: cT1-cT2 PCa; biopsy Gleason score ≤ 6; prostate-specific antigen ≤ 10 ng/mL; ≤ 1 positive biopsy core; and ≤ 50% core involvement compared favorably with other protocols. Area under the receiver operating curve analyses showed good predictive power of our AS criteria for the pathological and oncological end points of our study. CONCLUSION: Existing AS protocols do not satisfactorily predict insignificant PCas in our cohort, hence necessitating the need for new AS criteria in the era of robotic and local ablative surgeries. No patients in our cohort had biochemical recurrence, LNI, or ECE of their PCas when our protocol was applied.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfCLINICAL GENITOURINARY CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHCohort Studies-
dc.subject.MESHHumans-
dc.subject.MESHLymphatic Metastasis-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Grading*-
dc.subject.MESHNeoplasm Recurrence, Local-
dc.subject.MESHProstate/pathology-
dc.subject.MESHProstate/surgery-
dc.subject.MESHProstate-Specific Antigen/blood-
dc.subject.MESHProstatectomy/methods-
dc.subject.MESHProstatic Neoplasms/diagnosis*-
dc.subject.MESHProstatic Neoplasms/pathology-
dc.subject.MESHProstatic Neoplasms/surgery-
dc.subject.MESHRobotics-
dc.titleYonsei Criteria: A New Protocol for Active Surveillance in the Era of Robotic and Local Ablative Surgeries-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Urology (비뇨기과학)-
dc.contributor.googleauthorSey Kiat Lim-
dc.contributor.googleauthorKwang Hyun Kim-
dc.contributor.googleauthorTae-Young Shin-
dc.contributor.googleauthorByung Ha Chung-
dc.contributor.googleauthorSung Joon Hong-
dc.contributor.googleauthorYoung Deuk Choi-
dc.contributor.googleauthorKoon Ho Rha-
dc.identifier.doi10.1016/j.clgc.2013.04.024-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00319-
dc.contributor.localIdA01227-
dc.contributor.localIdA02168-
dc.contributor.localIdA03371-
dc.contributor.localIdA03607-
dc.contributor.localIdA04111-
dc.contributor.localIdA04402-
dc.relation.journalcodeJ00575-
dc.identifier.eissn1938-0682-
dc.identifier.pmid23810442-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S1558767313000852-
dc.subject.keywordGleason 6-
dc.subject.keywordProstate cancer-
dc.subject.keywordProstatectomy-
dc.subject.keywordRobot-
dc.subject.keywordlow risk-
dc.contributor.alternativeNameKim, Kwang Hyun-
dc.contributor.alternativeNameRha, Koon Ho-
dc.contributor.alternativeNameShin, Tae Young-
dc.contributor.alternativeNameLim, Sey Kiat-
dc.contributor.alternativeNameChung, Byung Ha-
dc.contributor.alternativeNameChoi, Young Deuk-
dc.contributor.alternativeNameHong, Sung Joon-
dc.contributor.affiliatedAuthorKim, Kwang Hyun-
dc.contributor.affiliatedAuthorRha, Koon Ho-
dc.contributor.affiliatedAuthorShin, Tae Young-
dc.contributor.affiliatedAuthorLim, Sey Kiat-
dc.contributor.affiliatedAuthorChung, Byung Ha-
dc.contributor.affiliatedAuthorChoi, Young Deuk-
dc.contributor.affiliatedAuthorHong, Sung Joon-
dc.rights.accessRightsnot free-
dc.citation.volume11-
dc.citation.number4-
dc.citation.startPage501-
dc.citation.endPage507-
dc.identifier.bibliographicCitationCLINICAL GENITOURINARY CANCER, Vol.11(4) : 501-507, 2013-
dc.identifier.rimsid34364-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Urology (비뇨의학교실) > 1. Journal Papers

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