Multi-layer Data to Improve Diagnosis, Predict Therapy Resistance and Suggest Targeted Therapies in HGSOC

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorTurku University Hospital

About this trial

Chemotherapy resistance is the greatest contributor to mortality in advanced cancers and severe challenges remain in finding effective treatment modalities to cancer patients with metastasized and relapsed disease. High-grade serous ovarian cancer (HGSOC) is typically diagnosed at a stage where the disease is already widely spread to the abdomen and current standard of practice treatment consists of surgery followed by platinum-taxane based chemotherapy and maintenance therapy. While 90% of HGSOC patients show no clinically detectable signs of cancer after surgery and chemotherapy, only 43% of the patients are alive five years after diagnosis because of chemoresistant cancer.

This prospective, observational trial focuses on revealing major mechanisms causing chemoresistance in HGSOG patients and derive personalized treatment regimens for chemotherapy resistant HGSOC patients. The investigators recruit newly diagnosed advanced stage HGSOC patients who are then thoroughly followed during their cancer treatment. Longitudinal sampling includes digitalized H\&E stained histology slides mainly collected during routine diagnostics, fresh tumor \& ascites samples for next-generation sequencing/proteomics (WGS, RNA-seq, DNA-methylation, ATAC-seq, ChIP-seq, mass cytometry, etc.) and ex vivo experiments, plasma samples for circulating tumor DNA (ctDNA) analyses. Broad range of clinical parameters such as laboratory and radiologic parameters (e.g., FDG PET/CT), given cancer treatments and their outcomes are collected. Radiomic analyses are performed to PET/CT and CT scans. Long-term patient derived organoid lines are established from fresh tumor tissues. Actionable genomic alterations are searched.

The general objective is to establish a clinically useful precision oncology approach based on multi-level data collected in longitudinal setting, and translate the most potent and validated discoveries into clinical use. DECIDER project will produce AI-powered diagnostic tools, cutting-edge software platforms for clinical decision-making, novel data analysis \& integration methods, and high-throughput ex vivo drug screening approaches.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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.

Trial design

Design model

Parallel

Treatments tested in this trial

  • WGS and RNA sequencing

    Genetic
  • circulating tumor DNA (ctDNA)

    Genetic
  • FDG PET/CT imaging

    Diagnostic test

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: HGSOC patients treated with Neoadjuvant chemotherapy (NACT)Other 3 interventions
Group B: HGSOC patients treated with primary debulking surgery (PDS)Other 3 interventions

Trial outcomes

Primary outcomes

1

Successful clinical translation

The magnitude of successful clinical translation is measured by the number of times project-derived personalized medicine has impacted patients care by application of novel and existing biomarkers and therapies.

Time frame
5 years
2

Successful prediction of patient outcome with AI methods

Proportion of patients whose disease outcome (PFS, OS) is predicted correctly with digital histopathology images, genomic data and routine laboratory values

Time frame
5 years

Secondary outcomes

1

Successful validation of potentially druggable genetic alterations

Number of potentially druggable genetic alterations found and validated with in-vitro methods

Time frame
5 years
2

Successful prediction of genomic features from tumor histology

Number of genomic features that can be successfully recognized from tumor histology

Time frame
5 years
3

Prediction of primary treatment response from tumor histology using H&E stained whole slide images and AI-based methods

Number of patients whose outcome (primary therapy outcome, PFS) is predicted correctly

Time frame
5 years
4

Establishment of an updated version of Chemoresponse score (CRS) for measuring histological effect in tumor tissue after chemotherapy

Predictive power of the updated CRS at interval surgery is compared with traditional CRS

Time frame
5 years

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Turku University Hospital

Lead sponsor

University of Helsinki

Collaborator