Histopathology images predict multi-omics aberrations and prognoses in colorectal cancer patients.
Pei-Chen TsaiTsung-Hua LeeKun-Chi KuoFang-Yi SuTsung-Lu Michael LeeEliana MarosticaTomotaka UgaiMelissa ZhaoMai Chan LauJuha P VäyrynenMarios GiannakisYasutoshi TakashimaSeyed Mousavi KahakiKana WuMingyang SongJeffrey A MeyerhardtAndrew T ChanJung-Hsien ChiangJonathan NowakShuji OginoKun-Hsing YuPublished in: Nature communications (2023)
Histopathologic assessment is indispensable for diagnosing colorectal cancer (CRC). However, manual evaluation of the diseased tissues under the microscope cannot reliably inform patient prognosis or genomic variations crucial for treatment selections. To address these challenges, we develop the Multi-omics Multi-cohort Assessment (MOMA) platform, an explainable machine learning approach, to systematically identify and interpret the relationship between patients' histologic patterns, multi-omics, and clinical profiles in three large patient cohorts (n = 1888). MOMA successfully predicts the overall survival, disease-free survival (log-rank test P-value<0.05), and copy number alterations of CRC patients. In addition, our approaches identify interpretable pathology patterns predictive of gene expression profiles, microsatellite instability status, and clinically actionable genetic alterations. We show that MOMA models are generalizable to multiple patient populations with different demographic compositions and pathology images collected from distinctive digitization methods. Our machine learning approaches provide clinically actionable predictions that could inform treatments for colorectal cancer patients.
Keyphrases
- copy number
- machine learning
- end stage renal disease
- mitochondrial dna
- free survival
- genome wide
- chronic kidney disease
- ejection fraction
- deep learning
- case report
- peritoneal dialysis
- prognostic factors
- gene expression
- convolutional neural network
- single cell
- high throughput
- optical coherence tomography
- patient reported outcomes