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Lavage of the Uterine Cavity for the Diagnosis of Ovarian and Tubal Carcinoma and Their Premalignant Changes.

Not Applicable
Completed
Conditions
Ovarian Epithelial Cancer
Interventions
Procedure: Lavage of the Cavum uteri and proximal fallopian tubes
Procedure: Liquid-PAP smear
Registration Number
NCT02062697
Lead Sponsor
Medical University of Vienna
Brief Summary

Epithelial Ovarian cancer (EOC) is the leading cause of death among gynaecologic malignancies in western civilized countries, with an estimated prevalence in Europe and the US of 752,600 in 2007 and 59,828 deaths annually.

State-of-the-art diagnostic tests for EOC include transvaginal ultrasonography and serum cancer antigen (CA-125) measurements; the specificity of these diagnostic tools however is low, and both tests are not effective enough at detecting EOC early enough to improve clinical outcomes. Definitive diagnosis of EOC still relies on histological or cytological confirmation. These findings underline the importance for an effective test for early detection of EOC.

In the current project we will obtain a lavage of the uterine cavity. It will be investigated whether cells from EOCs or genetic material from those cells can be detected in the lavage fluid.

Aim of this study:

There is a clear clinical need for a diagnosis test to detect EOC at an earlier stage.

Detailed Description

Epithelial Ovarian cancer is the leading cause of death among gynaecologic malignancies in western civilized countries, with an estimated prevalence in Europe and the US of 752,600 in 2007 and 59,828 deaths annually. Treatment and survival of the patients depend primarily on the stage of the disease. Of all EOC patients only 25% are diagnosed at an early stage while the tumour is confined to the pelvis. In these cases the five-year survival rate is 80% to 90% and the disease can often be cured by the combination of surgery and chemotherapy. Unfortunately, almost 75% of women affected have advanced stage disease with metastatic spread throughout the abdominal cavity or to retroperitoneal lymph nodes at the time of diagnosis; five-year survival rates drop to 10%-30% for advanced disease, despite maximum surgical effort and combination chemotherapy.

State-of-the-art diagnostic tests for EOC include transvaginal ultrasonography and serum cancer antigen (CA-125) measurements; the specificity of these diagnostic tools however is low, and both tests are not effective enough at detecting EOC early enough to improve clinical outcomes. Definitive diagnosis of EOC still relies on histological or cytological confirmation. These findings underline the importance for an effective test for early detection of EOC.

In the current project we will obtain a lavage of the uterine cavity. It will be investigated whether cells from EOCs or genetic material from those cells can be detected in the lavage fluid.

Aim of this study:

There is a clear clinical need for a diagnosis test to detect EOC at an earlier stage.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
50
Inclusion Criteria
  • suspected ovarian cancer
  • verified ovarian cancer
Read More
Exclusion Criteria
  • pregnant
  • incapacitated persons
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Ovarian Epithelial CancerLavage of the Cavum uteri and proximal fallopian tubes* Lavage of the Cavum uteri and proximal fallopian tubes * Liquid-PAP (Papanicolaou) smear
Ovarian Epithelial CancerLiquid-PAP smear* Lavage of the Cavum uteri and proximal fallopian tubes * Liquid-PAP (Papanicolaou) smear
Primary Outcome Measures
NameTimeMethod
Detection of EOCs by mutation analysis in the lavage of the uterine cavity.Day 1

If the adnexal tumor removed turns out to be an EOC, mutation analysis will be carried out applying the sensitive massively parallel sequencing method published by Kinde et al. Mutations in the following genes will be analysed: AKT1, APC, ARID1A, BRAF, CTNNB1, CSMD3, CDKN2A, EGFR, FBXW7, FAT3, FGFR2, KRAS, MLL2, NRAS, PTEN, PIK3CA, PIK3R1, PPP2R1A, PIK3R, RNF43, and TP53.

Secondary Outcome Measures
NameTimeMethod
Detection of EOCs by mutation analysis of the liquid-based Pap smear.Day 1

Obtaining material from the uterine cervix by applying a liquid-based Pap smear technique to directly compare the two sampling techniques - Lavage and liquid-based Pap.

Trial Locations

Locations (6)

University Hospitals Leuven - Department of Obstetrics and Gynaecology

🇧🇪

Leuven, Belgium

Medical University Vienna, Dptm. of Obstetrics & Gynaecology

🇦🇹

Vienna, Austria

Charles University, Pilsen - Medical Faculty Hospital, Department of Obstetrics and Gynecology

🇨🇿

Pilsen, Plzeň Region, Czechia

Charité University - Campus Virchow Clinic

🇩🇪

Berlin, Germany

Klinik Essen Mitte (KEM)

🇩🇪

Essen, Germany

Universitätsklinikum Hamburg-Eppendorf (UKE)

🇩🇪

Hamburg, Germany

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