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Validation and Clinical Utility of a Prediction Model for the Risk of Upstaging to Invasive Breast Cancer After a Biopsy Diagnosis Ductal Carcinoma In Situ.
Meurs, Claudia J C; van Bekkum, Sara; van Rosmalen, Joost; Menke-Pluijmers, Marian B E; Siesling, Sabine; Westenend, Pieter J.
Afiliação
  • Meurs CJC; Department of HTSR, University of Twente, Enschede, The Netherlands. c.j.c.meurs@utwente.nl.
  • van Bekkum S; CMAnalyzing, Zevenaar, The Netherlands. c.j.c.meurs@utwente.nl.
  • van Rosmalen J; Department of Surgery, Albert Schweitzer Hospital, Dordrecht, The Netherlands.
  • Menke-Pluijmers MBE; Department of Biostatistics, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Siesling S; Department of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Westenend PJ; Department of Surgery, Albert Schweitzer Hospital, Dordrecht, The Netherlands.
Ann Surg Oncol ; 30(12): 7069-7080, 2023 Nov.
Article em En | MEDLINE | ID: mdl-37541961
ABSTRACT

BACKGROUND:

This study aimed to validate the DCIS-upstage model, a previously developed model to predict the risk of upstaging to invasive breast cancer in patients with biopsy-proven ductal carcinoma in situ (DCIS) in a more recent cohort and to assess the model's clinical utility.

METHODS:

The model was validated in a registry cohort (n = 2269) and in an institution cohort (n = 302). A calibration plot was made, followed by a decision curve analysis (DCA). The model's area under the curve (AUC) was compared with the AUC of another published model and with the AUCs of new models using the risk factors of the DCIS-upstage model and additional risk factors.

RESULTS:

The DCIS-upstage model had an AUC of 0.67 at development; in the validation, the AUC was 0.65 in the registry cohort and 0.73 in the institution cohort. The DCA showed that the model has clinical utility. The other published model had an AUC of 0.66 in the institution cohort. Adding risk factors to the DCIS-upstage model slightly increased the AUC.

CONCLUSIONS:

The DCIS-upstage prediction model is valid in other cohorts. The model has clinical utility and may be used to select patients with biopsy-proven DCIS for sentinel lymph node biopsy.

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article