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      <dc:title>Development of a Novel NGS Methodology for Ultrasensitive Circulating Tumor DNA Detection as a Tool for Early-Stage Breast Cancer Diagnosis</dc:title>
      <dc:creator>Jiménez-Rodríguez, Begoña</dc:creator>
      <dc:creator>Alba-Bernal, Alfonso</dc:creator>
      <dc:creator>López-López, Esperanza</dc:creator>
      <dc:creator>Quirós-Ortega, María Elena</dc:creator>
      <dc:creator>Carbajosa, Guillermo</dc:creator>
      <dc:creator>Garrido-Aranda, Alicia</dc:creator>
      <dc:creator>Álvarez-Pérez, Martína</dc:creator>
      <dc:creator>Godoy-Ortiz, Ana</dc:creator>
      <dc:creator>Queipo-Ortuño, María Isabel</dc:creator>
      <dc:creator>Vicioso-Recio, Luis Prudencio</dc:creator>
      <dc:creator>Díaz-Córdoba, Gema</dc:creator>
      <dc:creator>Roldán-Díaz, María Dunia</dc:creator>
      <dc:creator>Velasco-Suelto, Jesús</dc:creator>
      <dc:creator>Hernando Melia, Cristina</dc:creator>
      <dc:creator>Bermejo, Begoña</dc:creator>
      <dc:creator>Julve-Parreño, Ana</dc:creator>
      <dc:creator>Lluch, Ana</dc:creator>
      <dc:creator>Pascual, Javier</dc:creator>
      <dc:creator>Comino-Méndez, Iñaki</dc:creator>
      <dc:creator>Alba-Conejo, Emilio</dc:creator>
      <dc:subject>Cancer</dc:subject>
      <dc:description>Breast cancer (BC) is the most prevalent cancer in women. While usually detected when localized, invasive procedures are still required for diagnosis. Herein, we developed a novel ultrasensitive pipeline to detect circulating tumor DNA (ctDNA) in a series of 75 plasma samples from localized BC patients prior to any medical intervention. We first performed a tumor-informed analysis to correlate the mutations found in tumor tissue and plasma. Disregarding the tumor data next, we developed an approach to detect tumor mutations in plasma. We observed a mutation concordance between the tumor and plasma of 29.50% with a sensitivity down to 0.03% in mutant variant allele frequency (VAF). We detected mutations in 33.78% of the samples, identifying eight patients with plasma-only mutations. Altogether, we determined a specificity of 86.36% and a positive predictive value of 88.46% for BC detection. We demonstrated an association between higher ctDNA median VAF and higher tumor grade, multiple plasma mutations with a likelihood of relapse and more frequent TP53 plasma mutations in hormone receptor-negative tumors. Overall, we have developed a unique ultra-sensitive sequencing workflow with a technology not previously employed in early BC, paving the way for its application in BC screening.</dc:description>
      <dc:date>2023-02-16T08:01:13Z</dc:date>
      <dc:date>2023-02-16T08:01:13Z</dc:date>
      <dc:date>2022-12-21</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Jiménez-Rodríguez B, Alba-Bernal A, López-López E, Quirós-Ortega ME, Carbajosa G, Garrido-Aranda A, Álvarez M, Godoy-Ortiz A, Queipo-Ortuño MI, Vicioso L, Díaz-Córdoba G, Roldán-Díaz MD, Velasco-Suelto J, Hernando C, Bermejo B, Julve-Parreño A, Lluch A, Pascual J, Comino-Méndez I, Alba E. Development of a Novel NGS Methodology for Ultrasensitive Circulating Tumor DNA Detection as a Tool for Early-Stage Breast Cancer Diagnosis. International Journal of Molecular Sciences. 2023; 24(1):146. c</dc:identifier>
      <dc:identifier>https://hdl.handle.net/10630/25968</dc:identifier>
      <dc:identifier>https://doi.org/10.3390/ijms24010146</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Atribución 4.0 Internacional</dc:rights>
      <dc:publisher>IOAP-MDPI</dc:publisher>
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