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Development of an artificial intelligence-derived histologic signature associated with adjuvant gemcitabine treatment outcomes in pancreatic cancer
- Source :
- Cell reports. Medicine, vol 4, iss 4
- Publication Year :
- 2023
- Publisher :
- Elsevier BV, 2023.
-
Abstract
- Pancreatic ductal adenocarcinoma (PDAC) has been left behind in the evolution of personalized medicine. Predictive markers of response to therapy are lacking in PDAC despite various histological and transcriptional classification schemes. We report an artificial intelligence (AI) approach to histologic feature examination that extracts a signature predictive of disease-specific survival (DSS) in patients with PDAC receiving adjuvant gemcitabine. We demonstrate that this AI-generated histologic signature is associated with outcomes following adjuvant gemcitabine, while three previously developed transcriptomic classification systems are not (n= 47). We externally validate this signature in an independent cohort of patients treated with adjuvant gemcitabine (n= 46). Finally, we demonstrate that the signature does not stratify survival outcomes in a third cohort of untreated patients (n= 161), suggesting that the signature is specifically predictive of treatment-related outcomes but is not generally prognostic. This imaging analysis pipeline has promise in the development of actionable markers in other clinical settings where few biomarkers currently exist.
- Subjects :
- screening and diagnosis
Carcinoma
pancreatic cancer
Deoxycytidine
Gemcitabine
General Biochemistry, Genetics and Molecular Biology
4.1 Discovery and preclinical testing of markers and technologies
Pancreatic Neoplasms
Detection
Treatment Outcome
Rare Diseases
Orphan Drug
Good Health and Well Being
Pancreatic Ductal
Artificial Intelligence
Humans
digital pathology
predictive biomarker
Digestive Diseases
Biomarkers
Cancer
Subjects
Details
- ISSN :
- 26663791
- Volume :
- 4
- Database :
- OpenAIRE
- Journal :
- Cell Reports Medicine
- Accession number :
- edsair.doi.dedup.....3f6b3af258cac837d7a079ae994f87d6
- Full Text :
- https://doi.org/10.1016/j.xcrm.2023.101013