Improving Endometrial Cancer Assessment by Combining Genomic Profiling and Surgical Assessment

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity Hospital, Gasthuisberg

About this trial

EUGENIE is a prospective multicentre interventional study, focused on improving endometrial cancer (EC) assessment by combining the new technique of genomic profiling with surgical extra uterine disease assessment. The investigators aim to correlate EC stage to each of the molecular subgroups of disease and thereby guide surgical treatment and staging of EC by determining the association between molecular classification and disease stage and evaluating if and how disease stage in each of the molecular subgroups associates with prognosis.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Voluntary written informed consent of the participant or their legally authorized representative has been obtained before any screening procedures

Women ≥ 18 years

First diagnosis of EC, all disease stages and all histo-types

Disqualifiers

Participant has a history of pelvic or para-aortic lymph node dissection or sampling, previous pelvic (and/or para-aortic) radiotherapy, previous neoadjuvant chemotherapy

Any disorder, which in the Investigator's opinion might jeopardise the participant's safety or compliance with the protocol

Any prior or concomitant treatment(s) that might jeopardise the participant's safety or that would compromise the integrity of the Study

Trial design

Design model

Single group

Treatments tested in this trial

  • total hysterectomy with bilateral salpingo-oophorectomy, lymph node staging and comprehensive peritoneal staging

    Procedure/Surgery

    Surgical treatment will consist of total hysterectomy with bilateral salpingo-oophorectomy according to international guidelines. In low- and intermediate-risk EC patients, staging will include a sentinel lymph node (SLN) procedure. In high intermediate-risk and high-risk EC patients, lymph node staging will involve SLN procedure and/or pelvic and para-aortic lymph node dissection (LND), depending on the local protocol. The Study-related procedures include infracolic omentectomy or two separate omental representative biopsies, biopsies of all suspicious lesions as well as six peritoneal sites (bladder, pouch of Douglas, bilateral paracolic gutter and bilateral diaphragm). Stage IV patients will be treated according to European guidelines. When feasible, full surgical intervention (i.e. debulking) is recommended. If this cannot be achieved, a radiologic and/or histologic confirmation of tumor spread beyond the uterus will be accepted.

Treatment groups

1,000 Participants
are divided into 1 treatment group
Group A: All women older than 18 newly diagnosed with endometrial cancer of all stages and histotypesExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Endometrial cancer stage

Endometrial cancer stage assessed according to the 2009 an 2023 International Federation of Gynecology and Obstetrics (FIGO) staging

Time frame
72 months
2

Molecular type of endometrial cancer

Tumor classification using the molecular classification as proposed by either ProMisE or TRANSPORTEC. Groups will be classified as follows: 1. MMR: Mismatch Repair Protein Status will be determined as a surrogate for microsatellite instability (MSI) by considering the immunohistochemical (IHC) staining of the MMR proteins. In case of loss of staining of one or more MMR proteins, the EC will be classified as MMR deficient (MMRd), otherwise, the carcinoma will be coded as MMR proficient (MMRp). 2. POLE: if the POLE exonuclease domain mutations (EDM) gene is mutated (i.e. a pathogenic mutation), the tumour will be classified as POLE. 3. p53 IHC: TP53 mutation status will be determined via IHC and in case of inconclusive p53 staining, also sequencing. 4. NSMP: a carcinoma that has not been stratified into groups 1), 2) or 3) will be categorized into the NSMP (no specific molecular profile or copy number low).

Time frame
72 months

Secondary outcomes

1

Overall survival

Overall survival

Time frame
72 months
2

Time to recurrence

Time to recurrence

Time frame
72 months

Other outcomes

Sponsors and contacts

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University Hospital, Gasthuisberg

Lead sponsor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Collaborator

University Medical Centre Maribor

Collaborator