Institut Català de la Salut
[Bernet L] Department of Pathology, Hospital Universitario del Vinalopó, Elche, Spain. [Hardisson D] Department of Pathology, Hospital Universitario La Paz, Madrid. Hospital La Paz Institute for health Research (IdiPAZ), Universidad Autónoma de Madrid. [Rodrigo M] Department of Pathology, Hospital Universitario de Burgos, Burgos, Spain. [Córdoba A] Department of Pathology, Hospital Universitario de Navarra, Navarra, Spain. [Sancho M] Department of Pathology, Hospital Universitario de Salamanca, Salamanca, Spain. [Peg V] Servei d’Anatomia Patològica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. Spanish Biomedical Research Network Centre in Oncology (CIBERONC), Madrid, Spain
Vall d'Hebron Barcelona Hospital Campus
2023-08-30T11:37:54Z
2023-08-30T11:37:54Z
2023-07-31
Breast cancer; Molecular subtype; Total tumor load
Cáncer de mama; Subtipo molecular; Carga tumoral total
Càncer de mama; Subtipus molecular; Càrrega tumoral total
Aims: To assess the impact of the molecular subtype (MS) on the total number of CK19 mRNA copies in all positive SLN (TTL) threshold, to predict non-SLN affectation, and to compare 5 years progression-free survival (PFS) according to the risk of recurrence (ROR) group by PAM50. Methods: Cohort with infiltrating breast cancer with intra-operative metastatic SLN detected by one-step nucleic acid amplification (OSNA) assay who underwent subsequent ALND. Logistic regression was used to assess a possible interaction between TTL and MS(Triple Negative, Her-2-Enriched, Luminal A, or Luminal B), or hormone receptors (HR: positive or negative) by immunohistochemistry (IMH). Cox regression was used to compare PFS and OS in the 3 ROR groups (high, medium, or low). Results: TTL was predictive of non-SLN affectation in both univariate (OR [95% CI]: 1.72 [1.43, 2.05], P < .001) and multivariate (1.55 [95% CI: 1.04, 2.32], P = .030) models, but MS-IMH or HR-IMH, and their interactions with TTL were not (best multivariate model: HR + main effect OR 1.16 [95% CI: 0.18, 7.64], P = .874; interaction OR: 1.04 [0.7, 1.55], P = .835; univariate model: HR + main effect OR: 1.44 [95% CI: 0.85, 2.44], P = .180). PFS was lower in the high-risk ROR group (81.1%) than in the low-risk group (93.9%) (HR: 3.68 [95 CI: 1.70, 7.94], P < .001). Conclusions: our results do not provide evidence to support the utilization of subtype-specific thresholds for TTL values to make therapeutic decisions on the axilla. The ROR group was predictive of 5 years-PFS.
This study was funded by Sysmex España, S.L.
Article
Published version
English
Mama - Càncer; Metàstasi limfàtica; Marcadors tumorals; DISEASES::Neoplasms::Neoplasms by Site::Breast Neoplasms; DISEASES::Neoplasms::Neoplastic Processes::Neoplasm Metastasis::Lymphatic Metastasis; ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Investigative Techniques::Anthropometry::Body Weights and Measures::Tumor Burden; ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de la mama; ENFERMEDADES::neoplasias::procesos neoplásicos::metástasis neoplásica::metástasis linfática; TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::técnicas de investigación::antropometría::pesos y medidas corporales::carga tumoral
SAGE Publications
Clinical Pathology;16
https://doi.org/10.1177/2632010X231183693
Attribution-NonCommercial 4.0 International
http://creativecommons.org/licenses/by-nc/4.0/
Articles científics - HVH [3440]