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Supervised machine learning model to predict oncotype DX risk category in patients over age 50.
Pawloski, Kate R; Gonen, Mithat; Wen, Hannah Y; Tadros, Audree B; Thompson, Donna; Abbate, Kelly; Morrow, Monica; El-Tamer, Mahmoud.
Afiliación
  • Pawloski KR; Breast Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Gonen M; Biostatistics Service, Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Wen HY; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Tadros AB; Breast Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Thompson D; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Abbate K; Breast Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Morrow M; Breast Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • El-Tamer M; Breast Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA. eltamerm@mskcc.org.
Breast Cancer Res Treat ; 191(2): 423-430, 2022 Jan.
Article en En | MEDLINE | ID: mdl-34751852
ABSTRACT

PURPOSE:

Routine use of the oncotype DX recurrence score (RS) in patients with early-stage, estrogen receptor-positive, HER2-negative (ER+/HER2-) breast cancer is limited internationally by cost and availability. We created a supervised machine learning model using clinicopathologic variables to predict RS risk category in patients aged over 50 years.

METHODS:

From January 2012 to December 2018, we identified patients aged over 50 years with T1-2, ER+/HER2-, node-negative tumors. Clinicopathologic data and RS results were randomly split into training and validation cohorts. A random forest model with 500 trees was developed on the training cohort, using age, pathologic tumor size, histology, progesterone receptor (PR) expression, lymphovascular invasion (LVI), and grade as predictors. We predicted risk category (low RS ≤ 25, high RS > 25) using the validation cohort.

RESULTS:

Of the 3880 tumors identified, 1293 tumors comprised the validation cohort in patients of median (IQR) age 62 years (56-68) with median (IQR) tumor size 1.2 cm (0.8-1.7). Most tumors were invasive ductal (80.3%) of low-intermediate grade (80.5%) without LVI (80.9%). PR expression was ≤ 20% in 27.3% of tumors. Specificity for identifying RS ≤ 25 was 96.3% (95% CI 95.0-97.4) and the negative predictive value was 92.9% (95% CI 91.2-94.4). Sensitivity and positive predictive value for predicting RS > 25 was lower (48.3 and 65.1%, respectively).

CONCLUSION:

Our model was highly specific for identifying eligible patients aged over 50 years for whom chemotherapy can be omitted. Following external validation, it may be used to triage patients for RS testing, if predicted to be high risk, in resource-limited settings.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Middle aged Idioma: En Revista: Breast Cancer Res Treat Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Middle aged Idioma: En Revista: Breast Cancer Res Treat Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos