Publication:
Sentinel lymph node biopsy in early stage endometrial cancer: a Turkish Gynecologic Oncology Group study (TRSGO-SLN-002)

dc.contributor.coauthorTaskin, Salih
dc.contributor.coauthorAltin, Duygu
dc.contributor.coauthorTokgozoglu, Nedim
dc.contributor.coauthorKarabuk, Emine
dc.contributor.coauthorTuran, Hasan
dc.contributor.coauthorTakmaz, Ozguc
dc.contributor.coauthorKahramanoglu, Ilker
dc.contributor.coauthorNaki, Mehmet Murat
dc.contributor.coauthorGungor, Mete
dc.contributor.coauthorKose, Faruk
dc.contributor.coauthorOrtac, Firat
dc.contributor.coauthorArvas, Macit
dc.contributor.coauthorAyhan, Ali
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorTaşkıran, Çağatay
dc.contributor.kuauthorVatansever, Doğan
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:52:54Z
dc.date.issued2020
dc.description.abstractObjective: The aim of this multicenter study was to evaluate the feasibility of sentinel lymph node (SLN) mapping in clinically uterine confined endometrial cancer. Methods: Patients who underwent primary surgery for endometrial cancer with an SLN algorithm were reviewed. Indocyanine green or blue dye was used as a tracer. SLNs and/or suspicious lymph nodes were resected. Side specific lymphadenectomy was performed when mapping was unsuccessful. SLNs were ultrastaged on final pathology. Results: 357 eligible patients were analyzed. Median age was 59 years. Median number of resected SLNs was 2 (range 1-12) per patient. Minimal invasive and open surgeries were performed in 264 (73.9%) and 93 (26.1%) patients, respectively. Indocyanine green was used in 231 (64.7%) and blue dye in 126 (35.3%) patients. The dyes were injected into the cervix in 355 (99.4%) patients. The overall and bilateral SLN detection rates were 91.9% and 71.4%, respectively. The mapping rates using indocyanine green or blue dye were comparable (P=0.526). There were 43 (12%) patients with lymphatic metastasis. The SLN algorithm was not able to detect 3 of 43 patients who had isolated paraaortic metastasis. After SLN biopsy, complete pelvic lymphadenectomy was performed in 286 (80.1%) patients. Sensitivity and negative predictive value were both 100% for the detection of pelvic lymph node metastases. In addition, 117 (32.8%) patients underwent completion paraaortic lymphadenectomy after SLN biopsy. In these patients, sensitivity for detecting metastases to pelvic and/or paraaortic lymph nodes was 90.3% with a negative predictive value of 96.6%. The risk of non-SLN involvement in patients with macrometastatic SLNs, micrometastatic SLNs, and isolated tumor cells in SLNs were 61.2%, 14.3% and 0%, respectively. Conclusions: SLN biopsy had good accuracy in detecting lymphatic metastasis. However, one-third of cases with metastatic SLNs also had non-SLN involvement and this risk increased to two-thirds of cases with macrometastatic SLNs. The effect of leaving these nodes in situ on survival should be evaluated in further studies.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue3
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume30
dc.identifier.doi10.1136/ijgc-2019-000847
dc.identifier.eissn1525-1438
dc.identifier.issn1048-891X
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85081149177
dc.identifier.urihttps://doi.org/10.1136/ijgc-2019-000847
dc.identifier.urihttps://hdl.handle.net/20.500.14288/14927
dc.identifier.wos531876000004
dc.keywordsSentinel lymph node
dc.keywordsEndometrial neoplasms
dc.keywordsLymphatic metastasis
dc.language.isoeng
dc.publisherBMJ Publishing Group
dc.relation.ispartofInternational Journal of Gynecological Cancer
dc.subjectOncology
dc.subjectObstetrics
dc.subjectGynecology
dc.titleSentinel lymph node biopsy in early stage endometrial cancer: a Turkish Gynecologic Oncology Group study (TRSGO-SLN-002)
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorTaşkıran, Çağatay
local.contributor.kuauthorVatansever, Doğan
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
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