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Evaluation of the outcome benefit conferred by intensive surveillance strategies in women with early-stage endometrial cancer

dc.contributor.authorKıran, Gürkan
dc.contributor.authorKesterson, Joshua P.
dc.contributor.authorKanis, Margaux Jenna
dc.contributor.authorGroman, Adrienne E.
dc.contributor.authorLele, Shashikant B.
dc.contributor.buuauthorÖzerkan, Kemal
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentKadın Hastalıkları ve Doğum Ana Bilim Dalı
dc.contributor.researcheridAAH-9791-2021
dc.contributor.scopusid6603345841
dc.date.accessioned2022-03-16T13:16:26Z
dc.date.available2022-03-16T13:16:26Z
dc.date.issued2011-03
dc.description.abstractIntroduction: The optimum follow-up regimen after treatment for early-stage endometrial cancer with curative intent is unknown. The National Comprehensive Cancer Network recommends a physical exam and vaginal cytology every three to six months for two years then at six to 12 month intervals with annual chest X-rays (CXR). However, there is debate as to whether intensive follow-up results in an improvement in outcomes for those with recurrent endometrial cancer. Objective: To determine if intensive surveillance for recurrent cancer in women with early-stage endometrial cancer improves their outcomes. Materials and Methods: The Roswell Park Cancer Institute tumor registry was used to identify patients with Stage I and II endometrial cancer initially diagnosed and treated over an 18-year period, who subsequently recurred. Clinico-pathological variables were abstracted. Patients were divided into two groups, depending on their mode of diagnosis of recurrent cancer: 1) routine screening, or 2) symptomatic. The outcomes between the two groups were compared. Results: Fifty-two patients met inclusion criteria. Twenty-three patients were diagnosed via routine screening methods and 29 were symptomatic at presentation. Groups were equally represented with respect to age, stage, grade, adjuvant therapy, site of recurrence (local, distant), and time to recurrence (p > 0.05). Median survival time was 79 months for those diagnosed during routine screening and 80 months for symptomatic patients (p > 0.05). Conclusion: Pap smear and CXR appear to be of limited utility as the present study has shown that women diagnosed as a result of intensive surveillance did not have a better outcome than those who presented when symptomatic.
dc.identifier.citationKesterson, I. vd. (2011). "Evaluation of the outcome benefit conferred by intensive surveillance strategies in women with early-stage endometrial cancer". Gynecologic Oncology, 121(1), Supplement 1, S11-S12.
dc.identifier.doi10.1016/j.ygyno.2010.12.032
dc.identifier.endpageS12
dc.identifier.issn0090-8258
dc.identifier.issue10, Supplement 1
dc.identifier.scopus2-s2.0-84898862874
dc.identifier.startpageS11
dc.identifier.urihttps://doi.org/10.1016/j.ygyno.2010.12.032
dc.identifier.urihttps://www.gynecologiconcology-online.net/article/S0090-8258(10)00915-7/fulltext
dc.identifier.urihttp://hdl.handle.net/11452/25100
dc.identifier.volume121
dc.identifier.wos000290292300026
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherAcademic Press Inc Elsevier Science
dc.relation.collaborationYurt içi
dc.relation.collaborationYurt dışı
dc.relation.journalGynaecological Oncology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectOncology
dc.subjectObstetrics & gynecology
dc.subjectEndometrial cancer
dc.subjectSurveillance
dc.subject.emtreeAdult
dc.subject.emtreeAged
dc.subject.emtreeArticle
dc.subject.emtreeCancer adjuvant therapy
dc.subject.emtreeCancer center
dc.subject.emtreeCancer diagnosis
dc.subject.emtreeCancer epidemiology
dc.subject.emtreeCancer recurrence
dc.subject.emtreeCancer screening
dc.subject.emtreeCancer staging
dc.subject.emtreeClinical evaluation
dc.subject.emtreeClinical feature
dc.subject.emtreeControlled study
dc.subject.emtreeEarly cancer
dc.subject.emtreeEndometrium cancer
dc.subject.emtreeFemale
dc.subject.emtreeFollow up
dc.subject.emtreeHuman
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMiddle aged
dc.subject.emtreeOutcome assessment
dc.subject.emtreePapanicolaou test
dc.subject.emtreePatient identification
dc.subject.emtreeThorax radiography
dc.subject.emtreeVagina cytology
dc.subject.emtreeAsymptomatic disease
dc.subject.emtreeDisease free survival
dc.subject.emtreeEarly diagnosis
dc.subject.emtreeEndometrium tumor
dc.subject.emtreeHealth survey
dc.subject.emtreeKaplan Meier method
dc.subject.emtreePathology
dc.subject.emtreeTime
dc.subject.emtreeTumor recurrence
dc.subject.emtreeVagina smear
dc.subject.meshAged
dc.subject.meshAsymptomatic diseases
dc.subject.meshDisease-free survival
dc.subject.meshEarly detection of cancer
dc.subject.meshEndometrial neoplasms
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshKaplan-Meier estimate
dc.subject.meshMiddle aged
dc.subject.meshNeoplasm recurrence, local
dc.subject.meshNeoplasm staging
dc.subject.meshPopulation surveillance
dc.subject.meshRadiography, thoracic
dc.subject.meshTime factors
dc.subject.meshVaginal smears
dc.subject.scopusFluorodeoxyglucose F 18; Positron Emission Tomography Computed Tomography; Uterine Cervical Neoplasms
dc.subject.wosOncology
dc.subject.wosObstetrics & gynecology
dc.titleEvaluation of the outcome benefit conferred by intensive surveillance strategies in women with early-stage endometrial cancer
dc.typeOther
dc.type.subtypeMeeting Abstract
dc.wos.quartileQ1 (Obstetrics & gynecology)
dc.wos.quartileQ2 (Oncology)
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Kadın Hastalıkları ve Doğum Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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