Clinical Trials Directory

Trials / Completed

CompletedNCT04817501

Phenotypic Spectrum of CTCs in Tumors of the Female Reproductive System

Phenotypic Spectrum of Circulating Tumor Cell Populations as Markers of Liquid Biopsy in Tumors of the Female Reproductive System

Status
Completed
Phase
Study type
Observational
Enrollment
150 (actual)
Sponsor
Tomsk National Research Medical Center of the Russian Academy of Sciences · Academic / Other
Sex
Female
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

The study evaluates the level and molecular profiles of different CTC populations as markers for predicting the risk of developing hematogenous metastases and the effectiveness of treatment in patients with tumors of the female reproductive system (breast cancer, endometrial cancer, and ovarian cancer). The primary objective are: 1. To assess the presence and number of different populations of CTCs at different time points (before biopsy, before surgery, and after surgery). 2. To assess the relationships of different CTCs populations prior to treatment initiation with the effects of neoadjuvant chemotherapy and the risks of recurrence and metastases. 3. To assess the molecular profiles of different CTCs populations in the blood and in ascitic fluid. The secondary objective is to compare the multicolor flow cytometry results with data of ultrasound, CT and/or MRI, serum tumor markers, and immunohistochemical studies in patients with breast cancer, endometrial cancer and ovarian cancer

Detailed description

The overall goal is to study the diagnostic and prognostic efficacy of various CTC populations as liquid biopsy markers in tumors of the female reproductive system (breast cancer, endometrial cancer, and ovarian cancer). Phase I study: Determination of different populations of CTCs in blood and ascitic fluid (if any) prior to treatment. The main objectives of the study: 1. To assess the presence and number of different CTC populations at different time points (before biopsy and before surgery) using multicolor flow cytometry. 2. To assess the relationships between different CTCs populations prior to treatment initiation with the effects of neoadjuvant chemotherapy and the risks of recurrence and metastases. 3. To assess the molecular profiles of different CTCs populations in the blood and in ascitic fluid. Additional research tasks: To compare the multicolor flow cytometry results with the data of ultrasound, CT and/or MRI, serum tumor markers, and immunohistochemical studies in patients with breast cancer, endometrial cancer, and ovarian cancer Methodology: Open-label, exploratory, single centre study. Blood and ascitic fluid collected from subjects (if available)

Conditions

Interventions

TypeNameDescription
OTHERTaking 5 ml of venous blood at different time intervals
OTHERTaking 5 ml EDTA-stabilized ascitic fluid sampled during laparoscopy if any

Timeline

Start date
2014-02-14
Primary completion
2022-12-01
Completion
2022-12-01
First posted
2021-03-26
Last updated
2023-01-25

Locations

1 site across 1 country: Russia

Source: ClinicalTrials.gov record NCT04817501. Inclusion in this directory is not an endorsement.