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Serous Endometrial Intraepithelial Carcinoma (SEIC): Prospective Registration Study

Serous Endometrial Intraepithelial Carcinoma (SEIC): Prospective Registration Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06677242
Acronym
SEIC
Enrollment
100
Registered
2024-11-06
Start date
2025-04-01
Completion date
2035-04-01
Last updated
2025-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

SEIC, Serous Endometrial Intraepithalial Carcinoma

Keywords

Sereus endometrial intraepithelial carcinoma, SEIC, Endometrial cancer, Premalignant neoplasms

Brief summary

Background: Serous endometrial intra-epithelial carcinoma (SEIC) is a rare condition affecting the lining of the uterus. It's a pre-cancerous change that might lead to cancer if not treated. Doctors aren't sure of the best way to manage it because it's so uncommon. A previous study looked at past cases in the Netherlands from 2012 to 2020. This study found that none of the 23 women with SEIC had their cancer spread during surgery, and none had a recurrence in the following three years. This suggests that a simpler surgery might be safe for patients with SEIC. Methods: Information on disease details from patients who agree to participate in our study will be collected. All participants will fill out online forms and health questionnaires at several points: when they join the study, and again at six months, two years, and five years after their diagnosis. During the years after diagnosis, various details like health status, test results, treatments will be checked in the electronic medical record. Results: This study is just starting, with the first patients expected to join on January 1, 2025. Conclusion: A large international study is created to track SEIC patients over time. This will help us learn more about the condition and improve treatment strategies.

Interventions

DIAGNOSTIC_TESTBlood sample (serum) for circulating tumor DNA and cervical smear for genome-wide methylation sequencing

These are additional tests, added to the observational study to collect information on tumor characteristics and to pursue early detection of this diagnosis.

Sponsors

Erasmus Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Serous endometrial intra-epithelial carcinoma (SEIC). * Women older than 18 years of age. * Women with understanding of Dutch or English language in reading and writing.

Exclusion criteria

* Diagnosis with a different type of endometrial neoplasm or invasive carcinoma. * Previous and/or current treatment for another malignancy (\<2 year before diagnosis of SEIC).

Design outcomes

Primary

MeasureTime frameDescription
Progression-free survival5 yearsSurvival without recurrence of endometrial neoplasm

Secondary

MeasureTime frameDescription
Overall survival5 years
Health-related quality of life5 yearsAssessed through EORTC questionnaires Assessed through three different questionnaires: EORTC-QLQ-C30 + QLQ-EN24 (together a total of 54 multiple-choice questions with a scale of 1-4 of severity of complaints) and EQ-5D-5L (multiple-choice, scale of severity, all different items will be entered in the digital database)
Adverse events5 yearsAny adverse event related to the treatment of SEIC

Countries

Netherlands

Contacts

Primary ContactCiska Slaager
ciskaslaager@gmail.com+31652377107

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 9, 2026