doxorubicin hydrochloride
Intercalates into DNA and inhibits topoisomerase II.
Adjuvant therapy for breast cancer (node-positive after resection).
Treatment of multiple cancers including:
-
-
Acute lymphoblastic leukemia (ALL)
-
Acute myeloblastic leukemia (AML)
-
Hodgkin and non-Hodgkin lymphoma
-
Metastatic cancers: breast, Wilms’ tumor, neuroblastoma, soft tissue and bone sarcomas, ovarian, bladder, thyroid, gastric, and bronchogenic carcinoma.
-
Single agent: 60–75 mg/m² IV every 21 days
In combination: 40–75 mg/m² IV every 21–28 days
Breast cancer (adjuvant): 60 mg/m² IV on day 1 every 21 days for 4 cycles with cyclophosphamide
Alopecia (92% incidence in AC regimen)
Nausea/Vomiting
Myelosuppression (leukopenia, thrombocytopenia)
Severe cardiac conditions or recent myocardial infarction
Persistent myelosuppression
Severe hepatic impairment (bilirubin > 5 mg/dL)
Hypersensitivity to doxorubicin
Cardiomyopathy and Arrhythmias
Secondary Malignancies
Extravasation and Tissue Necrosis
Severe Myelosuppression
Use in Patients with Hepatic Impairment
Tumor Lysis Syndrome
Radiation Sensitization and Radiation Recall
Embryofetal Toxicity