{ "abstract": "Pancreatic ductal adenocarcinoma (PDAC), with a 12% 5-year survival rate, is the most aggressive type of cancer. Early diagnosis for this pathology is rare, and conventional treatments such as surgery, radio- or chemotherapy, have little to no effect on reducing mortality. Machine learning (ML) approaches could be used to identify biomarkers that help clinicians stratify patients and improve treatment outcomes. However, most ML techniques perform poorly with incomplete data, which is usually the case in real-world settings, often forcing researchers to discard valuable information. In this study, unsupervised ML algorithms capable of dealing with missing modalities were applied to incomplete multi-omics data from PDAC patients to identify clinically meaningful patient subgroups. Through a large-scale clustering benchmark including six omics layers, we discovered two novel subgroups with statistically significant differences in survival and recurrence after surgery, particularly within the first two years, when most patient deaths occur, as well as distinct tumor mutational burden. Comprehensive multi-omics analyses revealed substantial molecular differences between patients in both groups, identified three methylation biomarkers to stratify patients, and highlighted dysregulation in key oncogenic pathways. Importantly, the identified groups are different from previous PDAC classifications, both in their patient composition, prognosis, and in the oncogenic gene pathway profiles exhibited. Using an independent cohort, we further demonstrated that both the prognostic value of these subtypes and their underlying biological characteristics are reproducible. These results could lead to better stratified treatment regimens to improve the prognosis of PDAC patients. Author summary: Pancreatic cancer has one of the highest mortality rates among all cancer types, and it is difficult to find common molecular characteristics across tumors that can be used to create new treatments for patients. Machine learning algorithms are been used to analyze the molecular data of cancer patients and identify similar groups, for example, patients that share the same mutations in specific genes. This information can then be used to create tailored therapies for individuals and obtain the best patient outcomes. We applied machine learning algorithms to molecular data from pancreatic cancer patients (e.g.,: DNA, mutations, proteins) and identified two novel groups, with one of the groups showing lower survival probability, and an increased risk of cancer recurrence compared with the other. Further analysis revealed key cellular pathways and that three molecules could be used to separate patients into the two groups. This opens avenues for therapies personalized for every individual, to ensure that pancreatic cancer patients receive the best care they can.", "abstract_shown": true, "affiliations": [ "Department of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway", "Oslo Centre for Biostatistics and Epidemiology (OCBE), University of Oslo, Oslo, Norway", "Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland" ], "article_type": "Research Article", "arxiv": null, "author_total": 4, "authors": [ { "affs": [ 0 ], "name": "Alejandra Paja-García" }, { "affs": [ 1 ], "name": "Rafael Romero-Becerra" }, { "affs": [ 2 ], "name": "Tero Aittokallio" }, { "name": "Alberto López" } ], "bibtex": "https://research.draconitic.com/paper/a55qtdzsf3331.bib", "cited_by": 0, "doi": "10.1371/journal.pcbi.1014735", "fulltext_url": "https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1014735", "id": "a55qtdzsf3331", "issns": [ "1553-7358" ], "landing_url": "https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1014735", "language": null, "licence": "CC-BY-4.0", "licence_label": "CC BY 4.0", "licence_source": "journal", "licence_url": "https://creativecommons.org/licenses/by/4.0/", "metadata_licence": null, "native_subjects": [ [ "openalex", "2730|Pancreatic and Hepatic Oncology Research" ], [ "plos", "/Biology and life sciences/Biochemistry/Biomarkers" ], [ "plos", "/Biology and life sciences/Biochemistry/Nucleic acids/DNA/DNA modification/DNA methylation" ], [ "plos", "/Biology and life sciences/Cell biology/Chromosome biology/Chromatin/Chromatin modification/DNA methylation" ], [ "plos", "/Biology and life sciences/Genetics/DNA/DNA modification/DNA methylation" ], [ "plos", "/Biology and life sciences/Genetics/Epigenetics/Chromatin/Chromatin modification/DNA methylation" ], [ "plos", "/Biology and life sciences/Genetics/Epigenetics/DNA modification/DNA methylation" ], [ "plos", "/Biology and life sciences/Genetics/Gene expression" ], [ "plos", "/Biology and life sciences/Genetics/Gene expression/Chromatin/Chromatin modification/DNA methylation" ], [ "plos", "/Biology and life sciences/Genetics/Gene expression/DNA modification/DNA methylation" ], [ "plos", "/Biology and life sciences/Taxonomy" ], [ "plos", "/Computer and information sciences/Data management/Taxonomy" ], [ "plos", "/Medicine and health sciences/Oncology/Cancers and neoplasms/Gastrointestinal tumors/Pancreatic cancer" ], [ "plos", "/Medicine and health sciences/Oncology/Carcinogenesis" ], [ "plos", "/Physical sciences/Chemistry/Chemical reactions/Methylation" ], [ "plos", "/Physical sciences/Mathematics/Applied mathematics/Algorithms" ], [ "plos", "/Research and analysis methods/Simulation and modeling/Algorithms" ] ], "openalex": "W7212171668", "pdf_url": "https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1014735&type=printable", "pmcid": null, "pmid": null, "published": "2026-09-10", "publisher": "Public Library of Science", "ris": "https://research.draconitic.com/paper/a55qtdzsf3331.ris", "sources": [ { "first_seen": "2026-10-30T12:17:56Z", "native_id": "10.1371/journal.pcbi.1014735", "source": "plos", "url": "https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1014735" } ], "subjects": [ { "field": "biochemistry", "origin": "plos:gene expression", "subfield": "molecular-biology" }, { "field": "biology", "origin": "plos:genetics", "subfield": "genetics-genomics" }, { "field": "medicine", "origin": "plos:cancers and neoplasms", "subfield": "oncology" } ], "title": "Biomarker discovery and patient stratification in pancreatic cancer using incomplete multi-omics data", "title_text": "Biomarker discovery and patient stratification in pancreatic cancer using incomplete multi-omics data", "type": "peer-reviewed", "updated_at": "2026-10-30T12:17:56Z", "url": "https://research.draconitic.com/paper/a55qtdzsf3331", "venue": "PLOS Computational Biology", "versions": [] }