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Selection of Optimal Adjuvant Chemotherapy and Targeted Therapy for Early Breast Cancer

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Treatment Use of an Anthracycline-Taxane Regimen ➤ In patients who can tolerate it, use of a regimen containing anthracycline-taxane is considered the optimal strategy for adjuvant chemotherapy, particularly for patients deemed to be at high risk.* Adding Gemcitabine or Capecitabine to an Anthracycline-Taxane Regimen ➤ The addition of gemcitabine or capecitabine to an anthracycline-taxane regimen is NOT recommended for adjuvant chemotherapy.* Optimal-Dose Anthracycline Regimen for Patients for Whom a Taxane Is Contraindicated ➤ For patients with high-risk disease who will not receive a taxane, an optimal- dose anthracycline three-drug regimen (cumulative dose of doxorubicin ≥240 mg/m 2 or epirubicin ≥600 mg/m 2 but ≤720 mg/m 2 ) that contains cyclophosphamide is recommended. The cumulative dose of doxorubicin in two-drug regimens should not exceed 240 mg/m 2 . Capecitabine in Patients Age ≥65 Years ➤ In patients age ≥65 years, capecitabine is NOT recommended as an adjuvant chemotherapy option in lieu of standard regimens such as doxorubicin- cyclophosphamide or cyclophosphamide-methotrexate-fluorouracil (with oral cyclophosphamide). Cyclophosphamide-Methotrexate-Fluorouracil As an Alternative To Doxorubicin-Cyclophosphamide ➤ For patients in whom anthracycline-taxane is contraindicated, cyclophosphamide-methotrexate-fluorouracil (with oral cyclophosphamide) is an acceptable chemotherapy alternative to doxorubicin-cyclophosphamide. • Of note, the ASCO Panel recommends classic cyclophosphamide-methotrexate- fluorouracil (oral cyclophosphamide days 1–14 with intravenous [IV] methotrexate- fluorouracil days 1 and 8, repeated once every 28 days for six cycles) as the default adjuvant cyclophosphamide-methotrexate-fluorouracil regimen. • However, the Panel also recognizes that an all-IV cyclophosphamide-methotrexate- fluorouracil regimen once every 21 days is often used in clinical practice and was accepted by some clinical trials (e.g., TAILORx; Trial Assigning Individualized Options for Treatment [Rx]) on the basis of convenience and tolerability despite the absence of efficacy data from randomized controlled trials.

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