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Using computer assisted image analysis to determine the optimal Ki67 threshold for predicting outcome of invasive breast cancer.
Tay, Timothy Kwang Yong; Thike, Aye Aye; Pathmanathan, Nirmala; Jara-Lazaro, Ana Richelia; Iqbal, Jabed; Sng, Adeline Shi Hui; Ye, Heng Seow; Lim, Jeffrey Chun Tatt; Koh, Valerie Cui Yun; Tan, Jane Sie Yong; Yeong, Joe Poh Sheng; Chow, Zi Long; Li, Hui Hua; Cheng, Chee Leong; Tan, Puay Hoon.
Afiliación
  • Tay TKY; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Thike AA; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Pathmanathan N; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Jara-Lazaro AR; Current affiliation: Westmead Breast Cancer Institute, Westmead Hospital, Westmead, NSW, Australia.
  • Iqbal J; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Sng ASH; Current affiliation: Q Solutions - Central Laboratories, Singapore Science Park One, Singapore.
  • Ye HS; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Lim JCT; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Koh VCY; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Tan JSY; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Yeong JPS; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Chow ZL; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Li HH; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Cheng CL; Department of Anatomical Pathology, Singapore General Hospital, Singapore.
  • Tan PH; Division of Medicine, Singapore General Hospital, Singapore.
Oncotarget ; 9(14): 11619-11630, 2018 Feb 20.
Article en En | MEDLINE | ID: mdl-29545924
ABSTRACT

BACKGROUND:

Ki67 positivity in invasive breast cancers has an inverse correlation with survival outcomes and serves as an immunohistochemical surrogate for molecular subtyping of breast cancer, particularly ER positive breast cancer. The optimal threshold of Ki67 in both settings, however, remains elusive. We use computer assisted image analysis (CAIA) to determine the optimal threshold for Ki67 in predicting survival outcomes and differentiating luminal B from luminal A breast cancers.

METHODS:

Quantitative scoring of Ki67 on tissue microarray (TMA) sections of 440 invasive breast cancers was performed using Aperio ePathology ImmunoHistochemistry Nuclear Image Analysis algorithm, with TMA slides digitally scanned via Aperio ScanScope XT System.

RESULTS:

On multivariate analysis, tumours with Ki67 ≥14% had an increased likelihood of recurrence (HR 1.941, p=0.021) and shorter overall survival (HR 2.201, p=0.016). Similar findings were observed in the subset of 343 ER positive breast cancers (HR 2.409, p=0.012 and HR 2.787, p=0.012 respectively). The value of Ki67 associated with ER+HER2-PR<20% tumours (Luminal B subtype) was found to be <17%.

CONCLUSION:

Using CAIA, we found optimal thresholds for Ki67 that predict a poorer prognosis and an association with the Luminal B subtype of breast cancer. Further investigation and validation of these thresholds are recommended.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Oncotarget Año: 2018 Tipo del documento: Article País de afiliación: Singapur

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Oncotarget Año: 2018 Tipo del documento: Article País de afiliación: Singapur
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