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        <identifier>oai:figshare.com:article/33717766</identifier>
        <datestamp>2026-09-14T04:31:26Z</datestamp>
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          <dc:title>Data Sheet 1_ctDNA- and cfDNA-based liquid biopsy in bladder cancer and urothelial carcinoma: bibliometric mapping and cross-database coverage analysis, 2008-2025.zip</dc:title>
          <dc:creator>Junhua Li (125998)</dc:creator>
          <dc:creator>Chenhao Tang (24867688)</dc:creator>
          <dc:creator>Longfei Yang (435484)</dc:creator>
          <dc:creator>Chen Song (216175)</dc:creator>
          <dc:creator>Huixian Pan (24867691)</dc:creator>
          <dc:subject>Oncology and Carcinogenesis not elsewhere classified</dc:subject>
          <dc:subject>bibliometrics</dc:subject>
          <dc:subject>bladder cancer</dc:subject>
          <dc:subject>cfDNA</dc:subject>
          <dc:subject>ctDNA</dc:subject>
          <dc:subject>liquid biopsy</dc:subject>
          <dc:subject>molecular residual disease</dc:subject>
          <dc:subject>urothelial carcinoma</dc:subject>
          <dc:description>Background&lt;p&gt;Circulating tumour DNA (ctDNA), cell-free DNA (cfDNA) and urinary tumour DNA are increasingly studied in bladder cancer and urothelial carcinoma. We mapped the development, knowledge structure and clinical emphasis of this ctDNA/cfDNA-centred literature and assessed its coverage across three bibliographic databases.&lt;/p&gt;Methods&lt;p&gt;Web of Science Core Collection (WoSCC), Scopus and PubMed/MEDLINE were searched on July 31, 2026, for records published in 2008-2025. Reviewer-expanded strategies included liquid biopsy, ctDNA/cfDNA, molecular residual disease, molecular relapse, tumour-informed assays, urinary DNA, methylation, TERT and FGFR3. WoSCC was the primary mapping database; Scopus and PubMed/MEDLINE were coverage comparators. Python, VOSviewer and CiteSpace were used for descriptive and network analyses. Newly retrieved WoSCC records underwent duplicate independent screening and full third-reviewer quality control.&lt;/p&gt;Results&lt;p&gt;The searches retrieved 1,903 WoSCC, 3,201 Scopus and 230 PubMed/MEDLINE records. After WoSCC deduplication and eligibility assessment, 494 records formed the main set and 698 formed a contextual set. The main set received 17,031 citations (median 19; interquartile range 7-42), and annual output reached 82 records in 2025. Scopus covered 456/494 main records and PubMed/MEDLINE covered 93/494. Among 557 newly assessed records, the reviewers initially agreed on 433 (77.7%; Cohen’s kappa, 0.620); all records then underwent third-reviewer full-text quality control.&lt;/p&gt;Conclusions&lt;p&gt;The expanded search identifies a larger DNA-focused literature than the original strategy and confirms unequal database coverage. Thematic clusters and citation bursts trace a shift from early methylation-marker research towards ctDNA-based molecular residual disease assessment and perioperative treatment stratification. Bibliometric prominence describes research activity, not diagnostic accuracy, predictive validity or treatment benefit.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-14T04:31:26Z</dc:date>
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          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fonc.2026.1906152.s001</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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