{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,12]],"date-time":"2026-10-12T06:48:17Z","timestamp":1791787697680,"version":"4.3.4"},"reference-count":152,"publisher":"Wiley","license":[{"start":{"date-parts":[[2026,10,11]],"date-time":"2026-10-11T00:00:00Z","timestamp":1791676800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,10,11]],"date-time":"2026-10-11T00:00:00Z","timestamp":1791676800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["pathsocjournals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["The Journal of Pathology"],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    Pretreatment prediction of neoadjuvant response remains an unresolved challenge in locally advanced rectal cancer, where management is moving towards risk\u2010adapted and response\u2010oriented treatment strategies. Prediction remains difficult because response reflects interacting tumour\u2010intrinsic, immune, stromal, and spatial processes that are incompletely captured by standard clinical and radiological assessment. From a technology\u2010centred perspective, in this Review we assess how molecular, spatial, image\u2010based, and artificial intelligence\u2010enabled approaches are being used to study and predict response to neoadjuvant treatment from pretreatment biopsies and how readily they may be translated into clinical workflows. Genomic profiling has its clearest current clinical role in identifying hypermutated immune\u2010responsive subgroups, whereas broader genomic, epigenomic, and immune\u2010repertoire markers remain largely investigational. Bulk transcriptomics has generated multiple response signatures with variable reproducibility but has consistently highlighted immune activation, interferon signalling, stromal remodelling, and epithelial\u2013mesenchymal transition as recurrent response\u2010associated programmes; its most feasible clinical route is likely through targeted expression panels rather than open\u2010ended transcriptome profiling. Higher\u2010resolution approaches such as spatial transcriptomic and proteomic platforms refine these observations by localising signals to tumour, immune, and stromal compartments and capturing therapy\u2010induced tissue reorganisation, but they are currently best positioned for deepening biological understanding and nominating rational treatment combinations for future testing. Established platforms such as digital pathology are closer to routine deployment as they build on clinically embedded workflows, although response\u2010prediction algorithms still require robust external validation, calibration, and regulatory\u2010grade implementation. Patient\u2010derived models provide functional systems for testing candidate biomarkers and resistance mechanisms. Multimodal artificial intelligence may support response prediction by identifying complementary signals across data types and distilling complex signatures into parsimonious models suitable for clinical translation. Progress will depend on harmonised, longitudinal, multi\u2010centre studies that couple biological depth with assay standardisation, model reduction, and prospective evidence that response predictors improve patient management. \u00a9 2026 The Author(s).\n                    <jats:italic>The Journal of Pathology<\/jats:italic>\n                    published by John Wiley &amp; Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.\n                  <\/jats:p>","DOI":"10.1002\/path.70127","type":"journal-article","created":{"date-parts":[[2026,10,12]],"date-time":"2026-10-12T06:29:46Z","timestamp":1791786586000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Molecular, spatial, and\n                    <scp>AI<\/scp>\n                    \u2010enabled technologies for predicting neoadjuvant therapy response in locally advanced rectal cancer"],"prefix":"10.1002","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2463-6412","authenticated-orcid":false,"given":"Gina F","family":"Boot","sequence":"first","affiliation":[{"name":"Department of Biomedical Engineering, Faculty of Medicine University of Basel  Allschwil Switzerland"},{"name":"Institute of Medical Genetics and Pathology University Hospital Basel  Basel Switzerland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4462-0941","authenticated-orcid":false,"given":"Cibele","family":"Masotti","sequence":"additional","affiliation":[{"name":"Molecular Oncology Center Hospital S\u00edrio\u2010Liban\u00eas  S\u00e3o Paulo Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Claudia","family":"Corr\u00f2","sequence":"additional","affiliation":[{"name":"Translational Research Center in Onco\u2010Hematology, Department of Medicine, Faculty of Medicine University of Geneva  Geneva 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