| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Bernet, L |
| dc.contributor.author | Hardisson, David |
| dc.contributor.author | Rodrigo, M |
| dc.contributor.author | Córdoba, A |
| dc.contributor.author | Sancho, M. |
| dc.contributor.author | Peg, Vicente |
| dc.date.accessioned | 2023-08-30T11:37:54Z |
| dc.date.available | 2023-08-30T11:37:54Z |
| dc.date.issued | 2023-07-31 |
| dc.identifier.citation | Bernet L, Hardisson D, Rodrigo M, Córdoba A, Sancho M, Peg V, et al. OSNA Total Tumor Load for the Prediction of Axillary Involvement in Breast Cancer Patients: Should We use Different Thresholds According to the Intrinsic Molecular Subtype? MOTTO Study. Clin Pathol. 2023 Jul 31;16:1-8. |
| dc.identifier.issn | 2632-010X |
| dc.identifier.uri | https://hdl.handle.net/11351/10185 |
| dc.description | Breast cancer; Molecular subtype; Total tumor load |
| dc.description.abstract | 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. |
| dc.language.iso | eng |
| dc.publisher | SAGE Publications |
| dc.relation.ispartofseries | Clinical Pathology;16 |
| dc.rights | Attribution-NonCommercial 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ |
| dc.source | Scientia |
| dc.subject | Mama - Càncer |
| dc.subject | Metàstasi limfàtica |
| dc.subject | Marcadors tumorals |
| dc.subject.mesh | Breast Neoplasms |
| dc.subject.mesh | Lymphatic Metastasis |
| dc.subject.mesh | Tumor Burden |
| dc.title | OSNA Total Tumor Load for the Prediction of Axillary Involvement in Breast Cancer Patients: Should We use Different Thresholds According to the Intrinsic Molecular Subtype? MOTTO Study |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1177/2632010X231183693 |
| dc.subject.decs | neoplasias de la mama |
| dc.subject.decs | metástasis linfática |
| dc.subject.decs | carga tumoral |
| dc.relation.publishversion | https://doi.org/10.1177/2632010X231183693 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [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 |
| dc.identifier.pmid | 37534372 |
| dc.identifier.wos | 001040565200001 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |