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        <identifier>oai:figshare.com:article/33919888</identifier>
        <datestamp>2026-09-18T04:34:23Z</datestamp>
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          <dc:title>Data Sheet 1_Plasma multi-omics reveals molecular remodeling and prognostic biomarkers in advanced breast cancer treated with trastuzumab deruxtecan.docx</dc:title>
          <dc:creator>Die Sang (17143669)</dc:creator>
          <dc:creator>Wenyu Yang (571352)</dc:creator>
          <dc:creator>Jinsong Liu (6516)</dc:creator>
          <dc:creator>Yumeng Li (5954978)</dc:creator>
          <dc:creator>Shanshan Zhao (1333206)</dc:creator>
          <dc:creator>Xue Wang (102830)</dc:creator>
          <dc:creator>Yurong Zhang (104163)</dc:creator>
          <dc:creator>Biyun Wang (303983)</dc:creator>
          <dc:creator>Man Li (81239)</dc:creator>
          <dc:creator>Peng Yuan (150866)</dc:creator>
          <dc:subject>Oncology and Carcinogenesis not elsewhere classified</dc:subject>
          <dc:subject>advanced breast cancer</dc:subject>
          <dc:subject>biomarkers</dc:subject>
          <dc:subject>metabolomics</dc:subject>
          <dc:subject>multi−omics integration</dc:subject>
          <dc:subject>proteomics</dc:subject>
          <dc:subject>trastuzumab deruxtecan</dc:subject>
          <dc:description>Background&lt;p&gt;Trastuzumab deruxtecan (T-DXd), a HER2-targeted antibody-drug conjugate, has demonstrated clinical activity in HER2-positive and HER2-low advanced breast cancer. However, treatment outcomes remain heterogeneous, and circulating molecular correlates of treatment and prognosis are incompletely defined.&lt;/p&gt;Methods&lt;p&gt;Twenty-nine patients receiving T-DXd were included in the clinical cohort, of whom 16 provided paired pre- and post-two-cycle plasma for multi-omics profiling. Proteomics used 4D-DIA LC-MS/MS; metabolomics used UHPLC-high-resolution MS in positive/negative modes. Treatment-associated features were identified by paired statistics, fold change, and multivariate criteria, followed by enrichment, correlation, joint pathway mapping, and exploratory PFS-oriented Cox/LASSO-Cox analyses.&lt;/p&gt;Results&lt;p&gt;Proteomics identified 4,444 proteins; 508 were differentially expressed (136 up, 372 down), enriched in translation/ribosome, complement/coagulation, acute-phase, cytoskeletal/adhesion, and lipid transport pathways. Metabolomics detected 3,596 features; 70 were differential (43 up, 27 down), enriched in amino acid, tryptophan, nucleotide/energy, and lipid metabolism. Cross-omics analysis revealed structured correlations and joint purine metabolism mapping. Exploratory baseline analyses selected six protein and four metabolite prognostic biomarkers for PFS visualization.&lt;/p&gt;Conclusion&lt;p&gt;Paired plasma multi-omics revealed T-DXd-associated proteomic and metabolic remodeling. The molecular patterns and PFS-associated biomarkers are hypothesis-generating and require validation in larger independent cohorts.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-18T04:34:23Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fonc.2026.1973097.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Data_Sheet_1_Plasma_multi-omics_reveals_molecular_remodeling_and_prognostic_biomarkers_in_advanced_breast_cancer_treated_with_trastuzumab_deruxtecan_docx/33919888</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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