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        <datestamp>2026-09-24T04:33:34Z</datestamp>
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          <dc:title>Table 1_Case Report: Discordance between RNA-identified ETV6::RET and clinically reportable DNA profiling in salivary gland secretory carcinoma.docx</dc:title>
          <dc:creator>Shogen Boku (22031390)</dc:creator>
          <dc:creator>Takao Fujisawa (413999)</dc:creator>
          <dc:creator>Tomofumi Sakagami (15240815)</dc:creator>
          <dc:creator>Shigenori Kadowaki (3473348)</dc:creator>
          <dc:creator>Hironaga Satake (7491545)</dc:creator>
          <dc:creator>Hisateru Yasui (8967746)</dc:creator>
          <dc:creator>Koushiro Ohtsubo (14981990)</dc:creator>
          <dc:creator>Yasushi Shimizu (15146145)</dc:creator>
          <dc:creator>Tomoyuki Otsuka (493153)</dc:creator>
          <dc:creator>Bunya Kuze (679969)</dc:creator>
          <dc:creator>Riu Yamashita (1612)</dc:creator>
          <dc:creator>Taro Shibuki (11898834)</dc:creator>
          <dc:creator>Yoshiaki Nakamura (3981626)</dc:creator>
          <dc:creator>Hideaki Bando (6286331)</dc:creator>
          <dc:creator>Takayuki Yoshino (616028)</dc:creator>
          <dc:creator>Milan Radovich (172973)</dc:creator>
          <dc:creator>Masao Yagi (25101985)</dc:creator>
          <dc:creator>Susumu Okano (5686604)</dc:creator>
          <dc:subject>Oncology and Carcinogenesis not elsewhere classified</dc:subject>
          <dc:subject>case report</dc:subject>
          <dc:subject>comprehensive genomic profiling</dc:subject>
          <dc:subject>DNA profiling</dc:subject>
          <dc:subject>ETV6::RET</dc:subject>
          <dc:subject>RNA sequencing</dc:subject>
          <dc:subject>salivary gland secretory carcinoma</dc:subject>
          <dc:description>&lt;p&gt;Secretory carcinoma of the salivary gland is a rare, fusion-driven malignancy in which kinase fusions can serve as therapeutic targets. We report a patient with an ETV6::RET-positive tumor who achieved a complete response to pralsetinib and subsequently developed resistance. Research whole-transcriptome sequencing (WTS) of the resistant lesion identified an expressed in-frame ETV6::RET transcript retaining the RET kinase domain, with 300 and 196 split reads at the two breakpoints and three discordant mate pairs; research whole-exome sequencing provided limited concordant DNA-level support. A clinically approved targeted DNA-based comprehensive genomic profiling assay applied to material from the same lesion detected RET intron 11 and ETV6 intron 6 rearrangement signals but did not report actionable ETV6::RET or RET p.L730V. Under the Japanese regulatory framework applicable when selpercatinib was considered, an approved in vitro diagnostic or medical device was required to confirm a RET fusion for non-lung, non-thyroid solid tumors. Research WTS did not constitute an approved companion diagnostic result, and the approved DNA report did not establish an actionable ETV6::RET finding; selpercatinib was therefore not initiated. When DNA profiling yields unresolved rearrangement signals, a clinically validated RNA-based fusion assay and an appropriate regulatory framework for treatment selection may improve access to matched therapy.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-24T04:33:34Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fonc.2026.1967793.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Table_1_Case_Report_Discordance_between_RNA-identified_ETV6_RET_and_clinically_reportable_DNA_profiling_in_salivary_gland_secretory_carcinoma_docx/33979492</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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