{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,10]],"date-time":"2026-08-10T19:40:53Z","timestamp":1786390853481,"version":"build-2736575974"},"reference-count":32,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2026,5,29]],"date-time":"2026-05-29T00:00:00Z","timestamp":1780012800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,5,29]],"date-time":"2026-05-29T00:00:00Z","timestamp":1780012800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Cancer Reports"],"published-print":{"date-parts":[[2026,6]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      The recent fifth edition of World Health Organization and International Consensus Classification in 2022 recognized\n                      <jats:italic>TP53<\/jats:italic>\n                      \u2010mutated myelodysplastic neoplasms (MDS) as a distinct entity requiring multi\u2010hit classification. Literatures indicate that\n                      <jats:italic>TP53<\/jats:italic>\n                      variant alle frequency (VAF) correlates with clinical outcomes. However, comprehensive studies that characterize the full mutation landscape and clinical correlations in Asian populations are still limited.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Aims<\/jats:title>\n                    <jats:p>\n                      This research aims to elucidate the mutation spectrum and baseline characteristics of\n                      <jats:italic>TP53<\/jats:italic>\n                      \u2010mutated MDS in a Chinese cohort, thereby enhancing clinical understanding and treatment approaches.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods and Results<\/jats:title>\n                    <jats:p>\n                      A total of 161\n                      <jats:italic>TP53<\/jats:italic>\n                      \u2010mutated patients from 1589 newly diagnosed MDS with next\u2010generation sequencing (NGS) data via a targeted 96\u2010gene sequencing panel were analyzed to assess genomic alterations. Among 161\n                      <jats:italic>TP53<\/jats:italic>\n                      \u2010mutated patients (10.1% of 1589 MDS cases), we identified a predominance of missense mutations (76.9%) and frequent co\u2010occurrence with epigenetic modifiers, notably\n                      <jats:italic>DNMT3A<\/jats:italic>\n                      (11.8%),\n                      <jats:italic>TET2<\/jats:italic>\n                      (10.6%), and\n                      <jats:italic>ASXL1<\/jats:italic>\n                      (9.3%). Critically,\n                      <jats:italic>TP53<\/jats:italic>\n                      VAF correlated strongly with disease severity parameters, including hemoglobin levels, blast percentage, karyotype, and International Prognostic Scoring System (IPSS), revised IPSS (IPSS\u2010R) risk and IPSS\u2010Molecular (IPSS\u2010M) classifications (all\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.05), suggesting that\n                      <jats:italic>TP53<\/jats:italic>\n                      VAF serves as an important biomarker for risk stratification. In addition, patients with multiple\n                      <jats:italic>TP53<\/jats:italic>\n                      mutations harbored significantly worse IPSS, IPSS\u2010R, and IPSS\u2010M risk classifications compared to those with a single\n                      <jats:italic>TP53<\/jats:italic>\n                      mutation.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      This study underscores the importance of\n                      <jats:italic>TP53<\/jats:italic>\n                      mutations in Asian MDS patients, contributing to genetic profiling in risk stratification and therapeutic decision\u2010making.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/cnr2.70584","type":"journal-article","created":{"date-parts":[[2026,5,29]],"date-time":"2026-05-29T15:54:35Z","timestamp":1780070075000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Genetic and Clinical Features in\n                    <i>TP53<\/i>\n                    \u2010Mutated Patients With Myelodysplastic Neoplasms: A Retrospective Study Based on Next\u2010Generation Sequencing Data"],"prefix":"10.1002","volume":"9","author":[{"ORCID":"https:\/\/orcid.org\/0009-0008-2510-6983","authenticated-orcid":false,"given":"Yanming","family":"Cheng","sequence":"first","affiliation":[{"name":"Zhejiang Provincial Key Laboratory of Pancreatic Disease The First Affiliated Hospital, Zhejiang University School of Medicine  Hangzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0005-7529-5215","authenticated-orcid":false,"given":"Lixia","family":"Liu","sequence":"additional","affiliation":[{"name":"Department of Medical Affairs Acornmed Biotechnology Co. 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Beijing China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0002-1246-7671","authenticated-orcid":false,"given":"Yu","family":"Gao","sequence":"additional","affiliation":[{"name":"Zhejiang Provincial Key Laboratory of Pancreatic Disease The First Affiliated Hospital, Zhejiang University School of Medicine  Hangzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0004-0340-7401","authenticated-orcid":false,"given":"Yifei","family":"Wang","sequence":"additional","affiliation":[{"name":"Zhejiang Provincial Key Laboratory of Pancreatic Disease The First Affiliated Hospital, Zhejiang University School of Medicine  Hangzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0006-7045-3816","authenticated-orcid":false,"given":"Wei","family":"Zhu","sequence":"additional","affiliation":[{"name":"Zhejiang Provincial Key Laboratory of Pancreatic Disease The First Affiliated Hospital, Zhejiang University School of Medicine  Hangzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0000-8844-1123","authenticated-orcid":false,"given":"Hong","family":"Chen","sequence":"additional","affiliation":[{"name":"Department of Medical Affairs Acornmed Biotechnology Co. 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