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The Ki67 dilemma: investigating prognostic cut-offs and reproducibility for automated Ki67 scoring in breast cancer.
Rewcastle, Emma; Skaland, Ivar; Gudlaugsson, Einar; Fykse, Silja Kavlie; Baak, Jan P A; Janssen, Emiel A M.
Afiliación
  • Rewcastle E; Department of Chemistry, Bioscience and Environmental Engineering, University of Stavanger, Stavanger, Norway. emma.rewcastle@sus.no.
  • Skaland I; Department of Pathology, Stavanger University Hospital, Stavanger, Norway. emma.rewcastle@sus.no.
  • Gudlaugsson E; Department of Pathology, Stavanger University Hospital, Stavanger, Norway.
  • Fykse SK; Department of Pathology, Stavanger University Hospital, Stavanger, Norway.
  • Baak JPA; Department of Pathology, Stavanger University Hospital, Stavanger, Norway.
  • Janssen EAM; Department of Pathology, Stavanger University Hospital, Stavanger, Norway.
Breast Cancer Res Treat ; 207(1): 1-12, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38797793
ABSTRACT

PURPOSE:

Quantification of Ki67 in breast cancer is a well-established prognostic and predictive marker, but inter-laboratory variability has hampered its clinical usefulness. This study compares the prognostic value and reproducibility of Ki67 scoring using four automated, digital image analysis (DIA) methods and two manual methods.

METHODS:

The study cohort consisted of 367 patients diagnosed between 1990 and 2004, with hormone receptor positive, HER2 negative, lymph node negative breast cancer. Manual scoring of Ki67 was performed using predefined criteria. DIA Ki67 scoring was performed using QuPath and Visiopharm® platforms. Reproducibility was assessed by the intraclass correlation coefficient (ICC). ROC curve survival analysis identified optimal cutoff values in addition to recommendations by the International Ki67 Working Group and Norwegian Guidelines. Kaplan-Meier curves, log-rank test and Cox regression analysis assessed the association between Ki67 scoring and distant metastasis (DM) free survival.

RESULTS:

The manual hotspot and global scoring methods showed good agreement when compared to their counterpart DIA methods (ICC > 0.780), and good to excellent agreement between different DIA hotspot scoring platforms (ICC 0.781-0.906). Different Ki67 cutoffs demonstrate significant DM-free survival (p < 0.05). DIA scoring had greater prognostic value for DM-free survival using a 14% cutoff (HR 3.054-4.077) than manual scoring (HR 2.012-2.056). The use of a single cutoff for all scoring methods affected the distribution of prediction outcomes (e.g. false positives and negatives).

CONCLUSION:

This study demonstrates that DIA scoring of Ki67 is superior to manual methods, but further study is required to standardize automated, DIA scoring and definition of a clinical cut-off.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Biomarcadores de Tumor / Antígeno Ki-67 Límite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: Breast Cancer Res Treat Año: 2024 Tipo del documento: Article País de afiliación: Noruega Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Biomarcadores de Tumor / Antígeno Ki-67 Límite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: Breast Cancer Res Treat Año: 2024 Tipo del documento: Article País de afiliación: Noruega Pais de publicación: Países Bajos