Gene expression signature-based prediction of lymph node metastasis in patients with endometrioid endometrial cancer

dc.contributor.authorKang, Sokbom
dc.contributor.authorThompson, Zachary J.
dc.contributor.authorMcClung, Emily C.
dc.contributor.authorAbdallah, Reem M.
dc.contributor.authorLee, Jae K.
dc.contributor.authorGonzález-Bosquet, Jesús
dc.contributor.authorWenham, Robert Michael
dc.contributor.authorChon, Hye-sook
dc.contributor.departmentObstetrics and Gynecology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:08:01Z
dc.date.available2025-01-24T12:08:01Z
dc.date.issued2018
dc.description.abstractObjective This study aimed to develop a prediction model for lymph node metastasis using a gene expression signature in patients with endometrioid-type endometrial cancer. Methods Newly diagnosed endometrioid-type endometrial cancer cases in which the patients had undergone lymphadenectomy during a surgical staging procedure were identified from a national dataset (N = 330). Clinical and pathologic data were extracted from patient medical records, and gene expression datasets of their tumors were used to create a 12-gene predictive model for lymph node metastasis. We used principal components analysis on a training set (n = 110) to develop multivariate logistic models to predict low-risk patients having a probability of lymph node metastasis of less than 4%. The model with the highest prediction performance was selected for an evaluation set (n = 112), which, in turn, was validated in an independent validation set (n = 108). Results The model applied to the evaluation set showed 100% sensitivity (90% confidence interval [CI], 74%-100%) and 42% specificity (90% CI, 34%-51%), which resulted in 100% negative predictive value (90% CI, 89%-100%). In the validation set, we confirmed that the model consistently showed 100% sensitivity (90% CI, 88%-100%), 42% specificity (90% CI, 32%-50%), and 100% negative predictive value (90% CI, 88%-100%). Conclusions Our 12-gene signature model is a useful tool for the identification of patients with endometrioid-type endometrial cancer at low risk of lymph node metastasis, particularly given that it can be used to analyze histologic tissue before surgery and used to tailor surgical options.
dc.identifier.doihttps://doi.org/10.1097/IGC.0000000000001152
dc.identifier.eid2-s2.0-85041465287
dc.identifier.pmid29194195
dc.identifier.urihttp://hdl.handle.net/10938/31683
dc.language.isoen
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofInternational Journal of Gynecological Cancer
dc.sourceScopus
dc.subjectCancer genomics
dc.subjectDiagnosis and staging
dc.subjectEndometrial cancer
dc.subjectPersonalized medicine
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectCarcinoma, endometrioid
dc.subjectEndometrial neoplasms
dc.subjectFemale
dc.subjectGene expression regulation, neoplastic
dc.subjectHumans
dc.subjectLymphatic metastasis
dc.subjectMicroarray analysis
dc.subjectMiddle aged
dc.subjectPredictive value of tests
dc.subjectPrognosis
dc.subjectRetrospective studies
dc.subjectSensitivity and specificity
dc.subjectTranscriptome
dc.subjectDna
dc.subjectRna
dc.subjectArticle
dc.subjectCancer diagnosis
dc.subjectCancer patient
dc.subjectCancer staging
dc.subjectCancer surgery
dc.subjectCohort analysis
dc.subjectControlled study
dc.subjectEndometrioid carcinoma
dc.subjectEndometrium cancer
dc.subjectGene expression
dc.subjectGene expression profiling
dc.subjectGene expression signature
dc.subjectHuman
dc.subjectHuman tissue
dc.subjectLow risk patient
dc.subjectLymph node dissection
dc.subjectLymph node metastasis
dc.subjectMajor clinical study
dc.subjectPredictive value
dc.subjectPrincipal component analysis
dc.subjectPriority journal
dc.subjectVery elderly
dc.subjectEndometrium tumor
dc.subjectGene expression regulation
dc.subjectGenetics
dc.subjectPathology
dc.subjectRetrospective study
dc.titleGene expression signature-based prediction of lymph node metastasis in patients with endometrioid endometrial cancer
dc.typeArticle

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