CV: ↓LVEF, QT interval prolongation.
Derm: palmar-plantar erythrodysesthesia, rash, dry skin, ERYTHEMA MULTIFORM (EM), nail disorders, STEVENS-JOHNSON SYNDROME (SJS), TOXIC EPIDERMAL NECROLYSIS (TEN).
GI: nausea, vomiting, ↑ liver enzymes, DIARRHEA, dyspepsia, HEPATOTOXICITY, stomatitis.
Hemat: neutropenia.
MS: pain.
Neuro: fatigue, insomnia.
Resp: dyspnea, INTERSTITIAL LUNG DISEASE (ILD).
HER2Positive Metastatic Breast Cancer (Past Therapy with an Anthracycline, a Taxane and Trastuzumab)
- PO (Adults): 1250 mg once daily on Days 121 of 21-day cycle; continue until disease progression or unacceptable toxicity; Concurrent use of strong CYP3A4 inhibitors: 500 mg once daily on Days 121 of 21-day cycle; continue until disease progression or unacceptable toxicity; Concurrent use of strong CYP3A4 inducers: Gradually titrate dose from 1250 mg once daily up to 4500 mg once daily as tolerated; administer dose on Days 121 of 21-day cycle and continue until disease progression or unacceptable toxicity.
Hepatic Impairment
- PO (Adults): Severe hepatic impairment: 750 mg once daily on Days 121 of 21-day cycle; continue until disease progression or unacceptable toxicity.
Hormone Receptor-Positive, HER2Positive Metastatic Breast Cancer (Hormone Therapy Indicated)
- PO (Adults): 1500 mg once daily on Days 121 of 21-day cycle; continue until disease progression or unacceptable toxicity; Concurrent use of strong CYP3A4 inhibitors: 500 mg once daily on Days 121 of 21-day cycle; continue until disease progression or unacceptable toxicity; Concurrent use of strong CYP3A4 inducers: Gradually titrate dose from 1500 mg once daily up to 5500 mg once daily as tolerated; administer dose on Days 121 of 21-day cycle and continue until disease progression or unacceptable toxicity.
Hepatic Impairment
- PO (Adults): Severe hepatic impairment: 1000 mg once daily on Days 121 of 21-day cycle; continue until disease progression or unacceptable toxicity.
Therapeutic Classification: antineoplastics
Pharmacologic Classification: enzyme inhibitors, kinase inhibitors
Absorption: Incompletely and variably absorbed following oral administration; levels ↑ by food.
Distribution: Unknown.
Protein Binding: >99%.
Metabolism/Excretion: Extensively metabolized by the liver via the CYP3A4 and CYP3A5 isoenzymes; <2% excreted by kidneys.
Half-life: 24 hr.