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Biomarkers for Adjuvant Endocrine and Chemotherapy in Early-Stage Breast Cancer

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5 Prosigna (PAM50) Recommendation 1.15 ➤ If a patient is postmenopausal and has breast cancer that is node- negative, the clinician may use the Prosigna test to guide decisions for adjuvant systemic chemotherapy. (Moderate recommendation; EB-I) Recommendation 1.16 ➤ If a patient is premenopausal, and has node-negative or node-positive breast cancer the clinician should NOT use the Prosigna test to guide decisions for adjuvant systemic chemotherapy. (Moderate recommendation; IC-Ins) Recommendation 1.17 ➤ If a patient is postmenopausal and has node-positive breast cancer with 1–3 positive nodes, the evidence is inconclusive to recommend the use of Prosigna test to guide decisions for adjuvant endocrine and chemotherapy. (Moderate recommendation; EB-I) Recommendation 1.18 ➤ If a patient has node-positive breast cancer with more than 3 positive nodes, evidence on the clinical utility of routine use of Prosigna test to guide decisions for adjuvant endocrine and chemotherapy is insufficient to recommend its use. (Strong recommendation; IC-Ins) Mammostrat ➤ There is insufficient evidence to recommend use of Mammostrat to guide decisions about adjuvant endocrine and chemotherapy. (Moderate recommendation; EB-I) Breast Cancer Index (BCI) ➤ If a patient has ER-positive, HER2-negative, node-negative breast cancer, the clinician may use the BCI to guide decisions for adjuvant endocrine and chemotherapy. (Moderate recommendation; EB-I) ➤ If a patient has ER-positive, HER2-negative, node-positive breast cancer, the clinician should NOT use the BCI to guide decisions about adjuvant endocrine and chemotherapy. (Strong recommendation; IC-Ins)

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