Evidence map›Paper›PMID 42436414›Full record

ArticleBMC cancer2026

Association of immunohistochemistry-based molecular subtypes with adnexal involvement in endometrial cancer.

Oğuz Kaan Köksal, Hande Nur Öncü, Firdevs Şahin Duran, Şahin Kaan Baydemir, Neslihan Öztürk, Gökçen Ege, Candost Hanedan, Vakkas Korkmaz

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Article in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Oğuz Kaan KöksalDepartment of Gynecologic Oncology, Ankara Etlik City Hospital, Ankara, 06170, Turkey. oguzkaan134@gmail.com.ORCID http://orcid.org/0000-0002-9159-7476
Hande Nur ÖncüDepartment of Gynecologic Oncology, Ankara Etlik City Hospital, Ankara, 06170, Turkey.
Firdevs Şahin DuranDepartment of Pathology, Ankara Etlik City Hospital, Ankara, Turkey.
Şahin Kaan BaydemirDepartment of Gynecologic Oncology, Ankara Etlik City Hospital, Ankara, 06170, Turkey.
Neslihan ÖztürkDepartment of Gynecologic Oncology, Ankara Etlik City Hospital, Ankara, 06170, Turkey.
Gökçen EgeDepartment of Gynecologic Oncology, Ankara Etlik City Hospital, Ankara, 06170, Turkey.
Candost HanedanDepartment of Gynecologic Oncology, Ankara Etlik City Hospital, Ankara, 06170, Turkey.
Vakkas KorkmazDepartment of Gynecologic Oncology, Lokman Hekim University Hospital, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdnexal involvement in endometrial cancer is traditionally regarded as an anatomical spread pattern within FIGO stage IIIA; however, its biological heterogeneity remains incompletely understood. The 2023 FIGO staging system distinguishes between favorable "synchronous" ovarian involvement (stage IA3) and true metastatic spread to the ovary (stage IIIA1), highlighting the biological heterogeneity of adnexal involvement. This study aimed to investigate the association between immunohistochemistry (IHC)-based molecular subtypes and adnexal involvement, together with relevant clinicopathological factors.

methodsThis retrospective, single-center study included patients with surgically staged endometrial cancer. Tumors were classified into p53-abnormal, mismatch repair-deficient (MMRd) and non-specific molecular profile (NSMP) subtypes based on immunohistochemistry. Associations between adnexal involvement and molecular subtypes, preoperative serum CA-125 levels, lymphovascular space invasion (LVSI) and other clinicopathological variables were analyzed.

resultsAmong 661 patients, adnexal involvement was identified in 3.8% (n = 25) and varied significantly across molecular subtypes (p < 0.001). In multivariable analysis, p53-abnormal tumors showed a strong independent association with adnexal involvement (aOR 5.15, 95% CI 1.87-14.19, p = 0.001), whereas NSMP tumors were associated with lower risk. Elevated preoperative CA-125 levels (aOR 1.01, p < 0.001) and the presence of LVSI (aOR 6.62, p < 0.001) were also independent predictors.

conclusionIHC-based molecular subtypes are significantly associated with adnexal involvement in endometrial cancer. Integrating molecular classification with clinicopathological factors may enhance more individualized surgical planning, particularly regarding ovarian preservation decisions.

Indexed as

Adnexa UteriBiomarkers, TumorEndometrial NeoplasmsAdultAgedAged, 80 and overFemaleHumansImmunohistochemistryMiddle AgedNeoplasm StagingPrognosisRetrospective StudiesTumor Suppressor Protein p53Biomarkers, TumorTumor Suppressor Protein p53Adnexal involvementEndometrial cancerImmunohistochemistryMolecular classificationRisk stratification

Identifiers

PMID42436414
PMCPMC13640117

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