{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,25]],"date-time":"2026-08-25T13:33:37Z","timestamp":1787664817959,"version":"build-2736575974"},"reference-count":35,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2025,8,20]],"date-time":"2025-08-20T00:00:00Z","timestamp":1755648000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["82371911"],"award-info":[{"award-number":["82371911"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["82372075"],"award-info":[{"award-number":["82372075"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["82402415"],"award-info":[{"award-number":["82402415"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Magnetic Resonance Imaging"],"published-print":{"date-parts":[[2025,12]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Bladder cancer (BCa) with variant histology (VH) is aggressive, leading to poor prognosis and resistance to neoadjuvant treatment (NAT). Preoperative identification of VH may be important for informing treatment options.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Purpose<\/jats:title>\n                    <jats:p>To develop and validate a multiparametric MRI\u2010based ensemble model to identify VH in BCa and explore its association with disease\u2010free survival (DFS) and NAT response.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Study Type<\/jats:title>\n                    <jats:p>Retrospective.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Subjects<\/jats:title>\n                    <jats:p>\n                      Six hundred twenty patients with pathologically confirmed BCa (median age, 65\u2009years [IQR: 56, 73], 145 female) from four centers who underwent preoperative MRI, were divided into a training (\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009311), internal validation (\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u200954) from Center 1, and three external validation datasets (\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u200985, 68, and 102, respectively). Two additional cohorts, DFS (\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u200975) and NAT (\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u200969) cohorts, were collected from Center 1 to evaluate prognosis.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Field Strength\/Sequence<\/jats:title>\n                    <jats:p>3T, non\u2010fat suppressed T2\u2010weighted imaging using fast spin echo, diffusion\u2010weighted imaging using single\u2010shot echo planar imaging, and T1\u2010weighted dynamic contrast\u2010enhanced sequence using 3D gradient echo sequence.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Assessment<\/jats:title>\n                    <jats:p>Habitat, radiomic, clinical, clinical\u2010radiomic based, and the VHRisk Score (VHRiS) models were constructed for evaluating VH. The prognostic value of VHRiS for DFS and pathological complete response (pCR) rate was further evaluated.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Statistical Tests<\/jats:title>\n                    <jats:p>\n                      Mann\u2013Whitney U test,\n                      <jats:italic>t<\/jats:italic>\n                      \u2010test, ROC analysis (AUC), Kaplan\u2013Meier curves, log\u2010rank test, and SHapley Additive exPlanations (SHAP) analysis.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>The VHRiS model demonstrated favorable accuracy (AUCs: training, 0.971; internal validation, 0.895; external validation, 0.898\u20130.974). Low\u2010risk patients (VHRiS \u2265\u20090.863) exhibited significantly longer DFS than high\u2010risk patients (4.20 months vs. 3.08\u2009months) in the DFS cohort (median follow\u2010up period: 13.19\u2009months [IQR: 6.54, 31.91]). They also showed a higher pCR rate than high\u2010risk patients (64% vs. 33%) in the NAT cohort.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Data Conclusions<\/jats:title>\n                    <jats:p>The VHRiS model may be a robust tool for identifying VH, and may offer a potential method for risk stratification and prognosis prediction in patients with BCa.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Levels of Evidence<\/jats:title>\n                    <jats:p>4.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Technical Efficacy Stage<\/jats:title>\n                    <jats:p>2.<\/jats:p>\n                  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