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 volunteersQualifiers
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
Parallel
Treatments tested in this trial
WGS and RNA sequencing
Geneticcirculating tumor DNA (ctDNA)
GeneticFDG PET/CT imaging
Diagnostic test
Treatment groups
Trial outcomes
Primary outcomes
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.
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
Secondary outcomes
Successful validation of potentially druggable genetic alterations
Number of potentially druggable genetic alterations found and validated with in-vitro methods
Successful prediction of genomic features from tumor histology
Number of genomic features that can be successfully recognized from tumor histology
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
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
Sponsors and contacts
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Turku University Hospital
Lead sponsor
University of Helsinki
Collaborator