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   <dc:title>A novel targeted RNA-Seq panel identifies a subset of adult patients with acute lymphoblastic leukemia with BCR-ABL1-like characteristics</dc:title>
   <dc:creator>Sánchez, Ricardo</dc:creator>
   <dc:creator>Ribera, Jordi</dc:creator>
   <dc:creator>Morgades, Mireia</dc:creator>
   <dc:creator>Ayala, Rosa</dc:creator>
   <dc:creator>Onecha, Esther</dc:creator>
   <dc:creator>Ruiz Heredia, Yanira</dc:creator>
   <dc:creator>Juárez Rufián, Alexandra</dc:creator>
   <dc:creator>Nicolás, Rodrigo de</dc:creator>
   <dc:creator>Sánchez Pina, José</dc:creator>
   <dc:creator>Vives, Susana</dc:creator>
   <dc:creator>Zamora, Lurdes</dc:creator>
   <dc:creator>Mercadal, Santiago</dc:creator>
   <dc:creator>Coll, Rosa</dc:creator>
   <dc:creator>Cervera, Marta</dc:creator>
   <dc:creator>Garcia, Olga</dc:creator>
   <dc:creator>Ribera, Josep Maria</dc:creator>
   <dc:creator>Martínez López, Joaquín</dc:creator>
   <dc:subject>Leucèmia limfocítica crònica</dc:subject>
   <dc:subject>Pronòstic mèdic</dc:subject>
   <dc:subject>Chronic lymphocytic leukemia</dc:subject>
   <dc:subject>Prognosis</dc:subject>
   <dc:description>BCR-ABL1-like B-cell precursor acute lymphoblastic leukemia (BCP-ALL) remains poorly characterized in adults. We sought to establish the frequency and outcome of adolescent and adult BCR-ABL1-like ALL using a novel RNA-Seq signature in a series of patients with BCP-ALL. To this end, we developed and tested an RNA-Seq custom panel of 42 genes related to a BCR-ABL1-like signature in a cohort of 100 patients with BCP-ALL and treated with risk-adapted ALL trials. Mutations related to BCR-ABL1-like ALL were studied in a panel of 33 genes by next-generation sequencing (NGS). Also, CRLF2 overexpression and IKZF1/CDKN2A/B deletions were analyzed. Twenty out of 79 patients (12-84 years) were classified as BCR-ABL1-like (25%) based on heatmap clustering, with significant overexpression of ENAM, IGJ, and CRLF2 (P &lt;= 0.001). The BCR-ABL1-like subgroup accounted for 29% of 15-60-year-old patients, with the following molecular characteristics: CRLF2 overexpression (75% of cases), IKZF1 deletions (64%), CDKN2A/B deletions (57%), and JAK2 mutations (57%). Among patients with postinduction negative minimal residual disease, those with the BCR-ABL1-like ALL signature had a higher rate of relapse and lower complete response duration than non-BCR-ABL1-like patients (P = 0.007). Thus, we have identified a new molecular signature of BCR-ABL1-like ALL that correlates with adverse prognosis in adult patients with ALL.</dc:description>
   <dc:date>2021-01-12T19:05:31Z</dc:date>
   <dc:date>2021-01-12T19:05:31Z</dc:date>
   <dc:date>2020-04-24</dc:date>
   <dc:date>2020-12-21T13:10:52Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>https://hdl.handle.net/2445/173078</dc:identifier>
   <dc:identifier>32332702</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.1038/s41408-020-0308-3</dc:relation>
   <dc:relation>Blood Cancer Journal, 2020, vol. 10, num. 4</dc:relation>
   <dc:relation>https://doi.org/10.1038/s41408-020-0308-3</dc:relation>
   <dc:rights>cc by (c) Sánchez et al., 2020</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>11 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Nature Publishing Group</dc:publisher>
   <dc:source>Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))</dc:source>
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