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      <dc:title>Pattern of recurrence of early breast cancer is different according to intrinsic subtype and proliferation index.</dc:title>
      <dc:creator>Ribelles, Nuria</dc:creator>
      <dc:creator>Jerez-Aragonés, José Manuel</dc:creator>
      <dc:creator>Pajares, Bella</dc:creator>
      <dc:creator>Vicioso-Recio, Luis Prudencio</dc:creator>
      <dc:creator>Jiménez-Rodríguez, Begoña</dc:creator>
      <dc:creator>De Luque, Vanessa</dc:creator>
      <dc:creator>Franco, Leónardo</dc:creator>
      <dc:creator>Gallego-Domínguez, Elena María</dc:creator>
      <dc:creator>Márquez, Antonia</dc:creator>
      <dc:creator>Álvarez, Martina</dc:creator>
      <dc:creator>Sánchez-Muñoz, Alfonso</dc:creator>
      <dc:creator>Pérez-Rivas, Luis G.</dc:creator>
      <dc:creator>Alba-Conejo, Emilio</dc:creator>
      <dc:creator>Ribelles, Nuria</dc:creator>
      <dc:subject>Mamas - Cáncer - Recidiva</dc:subject>
      <dc:subject>Marcadores tumorales</dc:subject>
      <dc:description>Articulo publicado en la revista Breast Cancer Research.&#xd;
Esta versión tiene Licencia Creative Commons CC-BY&#xd;
SÍ permite usos comerciales y SÍ permite obras derivadas</dc:description>
      <dc:description>Recurrence risk in breast cancer varies throughout the follow-up time. We examined if these changes&#xd;
are related to the level of expression of the proliferation pathway and intrinsic subtypes.&#xd;
Results: Luminal A displayed a slow risk increase, reaching its maximum after three years and then remained steady.&#xd;
Luminal B presented most of its relapses during the first five years. HER2-enriched tumors show a peak of recurrence&#xd;
nearly twenty months post-surgery, with a greater risk in Ki-67 ≥14%. However a second peak occurred at 72 months&#xd;
but the risk magnitude was greater in Ki-67 &lt;14%. Triple negative tumors with low proliferation rate display a smooth&#xd;
risk curve, but with Ki-67 ≥14% show sharp peak at nearly 18 months.&#xd;
Conclusions: Each intrinsic subtype has a particular pattern of relapses over time which change depending on the&#xd;
level of activation of the proliferation pathway assessed by Ki-67. These findings could have clinical implications both&#xd;
on adjuvant treatment trial design and on the recommendations concerning the surveillance of patients.</dc:description>
      <dc:date>2024-04-30T08:58:56Z</dc:date>
      <dc:date>2024-04-30T08:58:56Z</dc:date>
      <dc:date>2013-10-22</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Ribelles N, Perez-Villa L, Jerez JM, Pajares B, Vicioso L, Jimenez B, de Luque V, Franco L, Gallego E, Marquez A, Alvarez M, Sanchez-Muñoz A, Perez-Rivas L, Alba E. Pattern of recurrence of early breast cancer is different according to intrinsic subtype and proliferation index. Breast Cancer Res. 2013;15(5):R98. doi: 10.1186/bcr3559. PMID: 24148581; PMCID: PMC3978680.</dc:identifier>
      <dc:identifier>https://hdl.handle.net/10630/31184</dc:identifier>
      <dc:identifier>doi: 10.1186/bcr3559</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>BMC</dc:publisher>
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