Publication:
Reviving peritoneal cytology: Exploring its role in endometrial cancer molecular classification.

cris.virtualsource.author-orcid6243fa24-f8f4-481c-9673-a0c9a6576596
cris.virtualsource.author-orcid424204a4-c997-4dc2-9a7d-1e122d30d053
cris.virtualsource.author-orcid5e76d79b-c64d-4d3c-9b00-1afadeef0c39
cris.virtualsource.author-orcida9c0e93b-1c07-43a2-a9fd-6fe5886983ee
cris.virtualsource.author-orcid8673acf1-190d-4e1c-bf53-a63499da0aaa
cris.virtualsource.author-orcidcb6a5c2b-9f30-460d-bcea-7589d529f382
cris.virtualsource.author-orcid739973bf-27d2-4e55-932c-d9b5649868a0
cris.virtualsource.author-orcidef30bd1c-d112-4cb4-97d9-061644d0e154
datacite.rightsopen.access
dc.contributor.authorVilliger, Anna-Sophie
dc.contributor.authorZurbriggen, Selma
dc.contributor.authorImboden, Sara
dc.contributor.authorSolass, Wiebke
dc.contributor.authorChriste, Lucine Constance
dc.contributor.authorSaner, Flurina Anna-Carina Maria
dc.contributor.authorGmür, Andrea
dc.contributor.authorRau, Tilman T
dc.contributor.authorMueller, Michael
dc.contributor.authorSiegenthaler, Franziska Anna
dc.date.accessioned2024-10-26T17:07:10Z
dc.date.available2024-10-26T17:07:10Z
dc.date.issued2024-03
dc.description.abstractOBJECTIVE The prognostic significance of positive peritoneal cytology in endometrial cancer has long been debated. In 2009, the Fédération Internationale de Gynécologie et d'Obstétrique (FIGO) removed cytology as a staging criterion from the endometrial cancer staging system. However, there is still evidence that positive peritoneal cytology may decrease survival among patients with endometrial cancer. The aim of this study was to determine the prognostic significance of positive peritoneal cytology among the different molecular subgroups. METHODS This study included patients with endometrial cancer who underwent primary surgical treatment between 2004 and 2015 at the Bern University Hospital, Switzerland, with molecular classification of the primary tumor and peritoneal cytology performed. RESULTS A total, 250 patients with endometrial cancer were enrolled. Peritoneal cytology was assessed in 206 patients, of whom 24% were positive: 25% of the POLEmut, 16% of the MMRd, 41% of the p53abn, and 24% of the NSMP cases. The mean follow-up was 128.7 months. Presence of positive peritoneal cytology was associated with significantly decreased mean recurrence-free and overall survival in patients with p53abn (p = .003 and p = .001) and NSMP (p = .020 and p = .049) endometrial cancer. In multivariable Cox regression analysis, positive peritoneal cytology remained an independent predictor of recurrence (p = .033) and death (p = .008) in p53abn endometrial cancer patients. CONCLUSION Positive peritoneal cytology is associated with worse oncologic outcomes in NSMP and p53abn endometrial cancer and remains an independent predictor of recurrence and death in patients with p53abn endometrial cancer.
dc.description.numberOfPages8
dc.description.sponsorshipUniversitätsklinik für Frauenheilkunde
dc.description.sponsorshipInstitut für Gewebemedizin und Pathologie - Klinische Pathologie
dc.description.sponsorshipInstitut für Gewebemedizin und Pathologie
dc.identifier.doi10.48350/192120
dc.identifier.pmid38266401
dc.identifier.publisherDOI10.1016/j.ygyno.2024.01.006
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/173787
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofGynecologic oncology
dc.relation.issn1095-6859
dc.relation.organizationClinic of Gynaecology
dc.relation.organizationInstitute of Tissue Medicine and Pathology, Clinical Pathology
dc.relation.organizationInstitute of Tissue Medicine and Pathology
dc.subjectEndometrial cancer Molecular classification Overall survival Peritoneal cytology Recurrence rate Surgical treatment
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.subject.ddc500 - Science::570 - Life sciences; biology
dc.titleReviving peritoneal cytology: Exploring its role in endometrial cancer molecular classification.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage155
oaire.citation.startPage148
oaire.citation.volume182
oairecerif.author.affiliationUniversitätsklinik für Frauenheilkunde
oairecerif.author.affiliationUniversitätsklinik für Frauenheilkunde
oairecerif.author.affiliationInstitut für Gewebemedizin und Pathologie - Klinische Pathologie
oairecerif.author.affiliationInstitut für Gewebemedizin und Pathologie
oairecerif.author.affiliationUniversitätsklinik für Frauenheilkunde
oairecerif.author.affiliationUniversitätsklinik für Frauenheilkunde
oairecerif.author.affiliationUniversitätsklinik für Frauenheilkunde
oairecerif.author.affiliationUniversitätsklinik für Frauenheilkunde
oairecerif.author.affiliation2Institut für Gewebemedizin und Pathologie - Klinische Pathologie
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unibe.date.licenseChanged2024-01-25 09:01:35
unibe.description.ispublishedpub
unibe.eprints.legacyId192120
unibe.refereedtrue
unibe.subtype.articlejournal

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