A computational method for prioritizing targeted therapies in precision oncology: performance analysis in the SHIVA01 trial.
Istvan PetakMaud KamalAnna DirnerIvan BiecheRobert DocziOdette MarianiPeter FilotasAnne-Vincent SalomonBarbara VodicskaVincent ServoisEdit VarkondiDavid GentienDora TihanyiPatricia TrescaDora LakatosNicolas ServantJulia DeriPauline Du RusquecCsilla HegedusDiana Bello RoufaiRichard SchwabCelia DupainIstvan T Valyi-NagyChristophe Le TourneauPublished in: NPJ precision oncology (2021)
Precision oncology is currently based on pairing molecularly targeted agents (MTA) to predefined single driver genes or biomarkers. Each tumor harbors a combination of a large number of potential genetic alterations of multiple driver genes in a complex system that limits the potential of this approach. We have developed an artificial intelligence (AI)-assisted computational method, the digital drug-assignment (DDA) system, to prioritize potential MTAs for each cancer patient based on the complex individual molecular profile of their tumor. We analyzed the clinical benefit of the DDA system on the molecular and clinical outcome data of patients treated in the SHIVA01 precision oncology clinical trial with MTAs matched to individual genetic alterations or biomarkers of their tumor. We found that the DDA score assigned to MTAs was significantly higher in patients experiencing disease control than in patients with progressive disease (1523 versus 580, P = 0.037). The median PFS was also significantly longer in patients receiving MTAs with high (1000+ <) than with low (<0) DDA scores (3.95 versus 1.95 months, P = 0.044). Our results indicate that AI-based systems, like DDA, are promising new tools for oncologists to improve the clinical benefit of precision oncology.
Keyphrases
- artificial intelligence
- palliative care
- big data
- clinical trial
- genome wide
- machine learning
- deep learning
- end stage renal disease
- newly diagnosed
- ejection fraction
- study protocol
- human health
- advanced cancer
- phase ii
- peritoneal dialysis
- multiple sclerosis
- electronic health record
- dna methylation
- phase iii
- emergency department
- bioinformatics analysis
- copy number
- open label
- climate change
- risk assessment
- transcription factor
- gene expression
- double blind
- drug delivery
- squamous cell
- drug induced