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Systems Oncology Approach to Optimize Ovarian Cancer Treatment

Systems Oncology Approach to Optimize Ovarian Cancer Treatment

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06117384
Acronym
ONCOSYS-OVA
Enrollment
500
Registered
2023-11-07
Start date
2022-01-01
Completion date
2027-12-31
Last updated
2023-11-07

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

Conditions

Ovarian Cancer

Brief summary

The overall aim is to identify effective therapeutic strategies to ovarian cancer (OC) using serial tumor, ascites and blood samples, and carry out state-of-the-art sequencing approaches, functional assays and associated bioinformatics to understand mechanisms behind chemoresistance in OC and identify new treatment options for OC patients. In this observational trial, we will systematically collect, analyze and interpret functional, molecular and clinical data from real-world ovarian cancer patients.

Interventions

GENETICBiomolecular profiling

Molecular and functional analysis of biospecimens, including tumor-normal Whole-exome sequencing, bulk and single-cell RNAsequencing, spatial proteomics, functional testing.

Sponsors

Helsinki University Central Hospital
CollaboratorOTHER
University of Helsinki
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with ovarian cancer * Available tumor tissue/blood samples

Exclusion criteria

* Inability to consent to the study

Design outcomes

Primary

MeasureTime frameDescription
Recruitment and collection of real-world clinical data from ovarian cancer patients5 yearsProspective recruitment and collection of clinical data from 500 ovarian cancer patients. Fraction of patients from which the collection of clinical data including patient age, tumor stage, histological diagnoses have been collected.
Successful collection and translational analysis of biospecimens5 yearsFraction of the recruited patients, from which tumor, ascites, and/or peripheral blood samples that have been successfully collected and subjected to molecular profiling.

Secondary

MeasureTime frameDescription
Discovery of candidate prognostic and predictive biomarkers5 yearsNumber of clinical and/or molecular features which of statistically significantly correlate to patient treatment outcomes (response to chemotherapy by RECIST1.1, Progression Free survival, Overall Survival).

Countries

Finland

Contacts

Primary ContactAnniina Färkkilä, MD PhD
anniina.farkkila@helsinki.fi+358504272060

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026