Matrix decomposition in meta-analysis for extraction of adverse event pattern and patient-level safety profile.
Kentaro MatsuuraJun TsuchidaShuji AndoTakashi SozuPublished in: Pharmaceutical statistics (2021)
The purpose of assessing adverse events (AEs) in clinical studies is to evaluate what AE patterns are likely to occur during treatment. In contrast, it is difficult to specify which of these patterns occurs in each patient. To tackle this challenging issue, we constructed a new statistical model including nonnegative matrix factorization by incorporating background knowledge of AE-specific structures such as severity and drug mechanism of action. The model uses a meta-analysis framework for integrating data from multiple clinical studies because insufficient information is derived from a single trial. We demonstrated the proposed method by applying it to real data consisting of three Phase III studies, two mechanisms of action, five anticancer treatments, 3317 patients, 848 AE types, and 99,546 AEs. The extracted typical treatment-specific AE patterns coincided with medical knowledge. We also demonstrated patient-level safety profiles using the data of AEs that were observed by the end of the second cycle.
Keyphrases
- phase iii
- case report
- healthcare
- electronic health record
- systematic review
- clinical trial
- end stage renal disease
- big data
- open label
- phase ii
- chronic kidney disease
- magnetic resonance
- ejection fraction
- newly diagnosed
- magnetic resonance imaging
- prognostic factors
- wastewater treatment
- peritoneal dialysis
- computed tomography
- adverse drug
- data analysis
- randomized controlled trial
- mass spectrometry
- meta analyses
- contrast enhanced
- drug induced