Improving diagnosis and treatment for advanced ovarian cancer
Official title: Integration of Multiple Data Levels to Improve Diagnosis, Predict Treatment Response and Suggest Targets to Overcome Therapy Resistance in High-grade Serous Ovarian Cancer
Run by Turku University Hospital · NCT04846933 · Data updated 2026-11-12
This study is testing personalized treatment plans for newly diagnosed advanced ovarian cancer patients who may not respond well to standard chemotherapy to see if it can improve their outcomes.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 200 (estimated) |
| Sponsor | Turku University Hospital Government |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Turku) |
| Status | Recruiting |
| Started | February 1, 2012 |
| Main results expected | December 2027 |
| Study ends | December 2029 |
| Registry record updated | January 16, 2025 |
| Trial ID | NCT04846933 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are newly diagnosed advanced stage HGSOC patients treated at Turku University Hospital.
✕Probably not a fit
Patients under 18 years old or those in too poor a condition for active treatment will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to address chemotherapy resistance in high-grade serous ovarian cancer (HGSOC) by developing personalized treatment regimens for patients who are likely to respond poorly to standard therapies. It involves recruiting newly diagnosed advanced stage HGSOC patients and utilizing advanced techniques such as whole genome sequencing, RNA sequencing, and circulating tumor DNA analysis. The study will also integrate digital pathology and clinical data with AI methods to identify mechanisms of resistance and suggest targeted therapies. The ultimate goal is to enhance clinical decision-making and improve patient outcomes through personalized medicine approaches.
Why it matters
Potential benefit: If successful, this study could lead to more effective, personalized treatment options for patients with chemotherapy-resistant ovarian cancer.
How similar studies have gone: Other studies have shown promise in using personalized medicine approaches for cancer treatment, suggesting potential success for this novel approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with a suspected ovarian cancer diagnosis treated at the Turku University Hospital * Ability to understand and the willingness to sign a written informed consent document Exclusion Criteria: * Age \<18 years, too poor condition for active treatment (surgery, chemotherapy) * FDG PET/CT scan is not performed for patients with diabetes mellitus and poor glucose balance.
Where it's running
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Turku University Hospital
Turku, Finland Recruiting
Study contacts
- Principal investigator: Johanna Hynninen, MD, PhD — Turku University Hospital
- Study coordinator: Johanna Hynninen
- Email: johanna.hynninen@utu.fi
- Phone: +358 50 5383554
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This study is testing if adjusting the dose of carboplatin based on a blood marker can help women with relapsed ovarian cancer feel better and have fewer side effects from treatment.
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Using a uterine wash and a blood protein test to find ovarian cancer early
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.