TARCEVA
What it isEGFR tyrosine-kinase inhibitor; EGFR-mutant lung cancer and pancreatic cancer.
Why this oneIts remaining distinctive role is combination therapy for pancreatic cancer; osimertinib has displaced it in most EGFR-mutant lung cancer.
What limits itAcneiform rash, diarrhea, and interstitial lung disease can end use; PPIs reduce absorption.
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| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Metastatic NSCLC (EGFR exon 19 del or exon 21 L858R) | Adults | 150 mg QD | 150 mg QD | 150 mg QD |
| Pancreatic cancer (with gemcitabine) | Adults | 100 mg QD | 100 mg QD | 100 mg QD |
Renal Withhold and consider discontinuation for severe (grade 3-4) renal toxicity; monitor renal function/electrolytes
Hepatic Withhold/consider discontinuation for severe or worsening liver tests; caution with pre-existing hepatic impairment or biliary obstruction
Pregnancy Can cause fetal harm; advise contraception and of potential risk to fetus
Lactation Do not breastfeed during treatment and for 2 weeks after final dose
NO BOXED WARNINGS
Principal riskInterstitial lung disease; superseded by osimertinib
Cost, est. cash$50–$10,000/month or cycle
Generic entry2014
Legacy pregnancy categoryD
Defining liabilityMyelosuppression and agent-specific hepatic, cardiac, pulmonary, neurologic or reproductive toxicity require oncology monitoring.

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