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   <dc:title>Predictive and prognostic value of total tumor load in sentinel lymph nodes in breast cancer patients after neoadjuvant treatment using one-step nucleic acid amplification : the NEOVATTL study</dc:title>
   <dc:creator>Vieites, B.</dc:creator>
   <dc:creator>López-García, M.</dc:creator>
   <dc:creator>Martín-Salvago, M.D.</dc:creator>
   <dc:creator>Ramírez Tortosa, César Luis</dc:creator>
   <dc:creator>Rezola, R.</dc:creator>
   <dc:creator>Sancho, M.</dc:creator>
   <dc:creator>López Vilaró, Laura</dc:creator>
   <dc:creator>Villardell, F.</dc:creator>
   <dc:creator>Burgués, Octavio</dc:creator>
   <dc:creator>Fernández-Rodriguez, B.</dc:creator>
   <dc:creator>Alfaro, L.</dc:creator>
   <dc:creator>Peg, Vicente</dc:creator>
   <dc:subject>Breast cancer</dc:subject>
   <dc:subject>Disease-free survival</dc:subject>
   <dc:subject>Neoadjuvant systemic therapy</dc:subject>
   <dc:subject>OSNA</dc:subject>
   <dc:subject>Sentinel lymph node</dc:subject>
   <dc:subject>Total tumor load</dc:subject>
   <dcterms:abstract>Altres ajuts: Sysmex España S.L.</dcterms:abstract>
   <dcterms:abstract>Objective: To evaluate the predictive and prognostic value of total tumor load (TTL) in sentinel lymph nodes (SLNs) in patients with infiltrating breast cancer after neoadjuvant systemic therapy (NST). Methods: This retrospective multicenter study used data from a Spanish Sentinel Lymph Node database. Patients underwent intraoperative SLN biopsy after NST. TTL was determined from whole nodes using a one-step nucleic acid amplification (OSNA) assay and defined as the total sum of CK19 mRNA copies in all positive SLNs. Cox-regression models identified independent predictive variables, which were incorporated into a nomogram to predict axillary non-SLN metastasis, and identified prognostic variables for incorporation into a disease-free survival (DFS) prognostic score. Results: A total of 314 patients were included; most had no lymph node involvement prior to NST (cN0; 75.0% of patients). Most received chemotherapy with or without biologic therapy (91.7%), and 81 patients had a pathologic complete response. TTL was predictive of non-SLN involvement (area under the concentration curve = 0.87), and at a cut-off of 15,000 copies/µL had a negative predictive value of 90.5%. Nomogram parameters included log (TTL + 1), maximum tumor diameter and study-defined NST response. TTL was prognostic of disease recurrence and DFS at a cut-off of 25,000 copies/µL. After a 5-year follow-up, DFS was higher in patients with ≤ 25,000 copies/µL than those with.</dcterms:abstract>
   <dcterms:issued>2021</dcterms:issued>
   <dc:type>Article</dc:type>
   <dc:relation>Clinical &amp; translational oncology ; Vol. 23 Núm. 7 (july 2021), p. 1377-1385</dc:relation>
   <dc:rights>open access</dc:rights>
   <dc:rights>Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.</dc:rights>
   <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:publisher/>
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