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The use of automated Ki67 analysis to predict Oncotype DX risk-of-recurrence categories in early-stage breast cancer.
Thakur, Satbir Singh; Li, Haocheng; Chan, Angela M Y; Tudor, Roxana; Bigras, Gilbert; Morris, Don; Enwere, Emeka K; Yang, Hua.
Afiliación
  • Thakur SS; Department of Oncology, University of Calgary, Calgary, Alberta, Canada.
  • Li H; Translational Laboratories, Tom Baker Cancer Center, Calgary, Alberta, Canada.
  • Chan AMY; Department of Oncology, University of Calgary, Calgary, Alberta, Canada.
  • Tudor R; Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada.
  • Bigras G; Translational Laboratories, Tom Baker Cancer Center, Calgary, Alberta, Canada.
  • Morris D; Department of Oncology, University of Calgary, Calgary, Alberta, Canada.
  • Enwere EK; Department of Pathology and Laboratory Medicine, University of Alberta, Edmonton, Alberta, Canada.
  • Yang H; Department of Oncology, University of Calgary, Calgary, Alberta, Canada.
PLoS One ; 13(1): e0188983, 2018.
Article en En | MEDLINE | ID: mdl-29304138
Ki67 is a commonly used marker of cancer cell proliferation, and has significant prognostic value in breast cancer. In spite of its clinical importance, assessment of Ki67 remains a challenge, as current manual scoring methods have high inter- and intra-user variability. A major reason for this variability is selection bias, in that different observers will score different regions of the same tumor. Here, we developed an automated Ki67 scoring method that eliminates selection bias, by using whole-slide analysis to identify and score the tumor regions with the highest proliferative rates. The Ki67 indices calculated using this method were highly concordant with manual scoring by a pathologist (Pearson's r = 0.909) and between users (Pearson's r = 0.984). We assessed the clinical validity of this method by scoring Ki67 from 328 whole-slide sections of resected early-stage, hormone receptor-positive, human epidermal growth factor receptor 2-negative breast cancer. All patients had Oncotype DX testing performed (Genomic Health) and available Recurrence Scores. High Ki67 indices correlated significantly with several clinico-pathological correlates, including higher tumor grade (1 versus 3, P<0.001), higher mitotic score (1 versus 3, P<0.001), and lower Allred scores for estrogen and progesterone receptors (P = 0.002, 0.008). High Ki67 indices were also significantly correlated with higher Oncotype DX risk-of-recurrence group (low versus high, P<0.001). Ki67 index was the major contributor to a machine learning model which, when trained solely on clinico-pathological data and Ki67 scores, identified Oncotype DX high- and low-risk patients with 97% accuracy, 98% sensitivity and 80% specificity. Automated scoring of Ki67 can thus successfully address issues of consistency, reproducibility and accuracy, in a manner that integrates readily into the workflow of a pathology laboratory. Furthermore, automated Ki67 scores contribute significantly to models that predict risk of recurrence in breast cancer.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Procesamiento de Imagen Asistido por Computador / Neoplasias de la Mama / Antígeno Ki-67 Tipo de estudio: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2018 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Procesamiento de Imagen Asistido por Computador / Neoplasias de la Mama / Antígeno Ki-67 Tipo de estudio: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2018 Tipo del documento: Article País de afiliación: Canadá