Low Dose Daily Erlotinib in Combination With High Dose Twice Weekly Erlotinib in Patients With EGFR-Mutant Lung Cancer

Inclusion Criteria:

MSKCC pathologically-proven diagnosis locally advanced Stage III not amenable to definitive, curative treatment or Stage IV or recurrent non-small cell lung cancer
Documented presence of EGFR mutation confirmed by MSKCC or a local facility.
No prior treatment with erlotinib, gefitinib, or other EGFR tyrosine kinase inhibitors
Age ≥ 18 years
Measurable (RECIST 1.1) indicator lesion not previously irradiated.
Karnofsky Performance Status ≥ 70%
Ability to take oral medications
A negative serum pregnancy test obtained within 4 weeks prior to the start of treatment in all women of child-bearing potential.
All women of child bearing potential and sexually active men must agree to use adequate methods of birth control throughout the study which includes use of oral contraceptives with an additional barrier methods, double barrier methods, Depo-Provera, permanent sterilization of patient or partner or total abstinence.

Expansion A:

brain metastases or leptomeningeal not previously treated with radiation or surgery

Exclusion Criteria:

Inadequate recovery from any toxicity related to prior treatment (to Grade 2 or baseline).
Inadequate hematologic function defined as ANC < 1000 cells/mm³, Platelet count <75,000/mm³ or Hemoglobin <9.0g/dL.
Inadequate hepatic function defined by AST/ALT >3x upper limit of normal (ULN), Total bilirubin>2x ULN, Alkaline phosphatase >3x ULN.
Symptomatic brain metastasis requiring radiation therapy or escalating doses of steroids.
Patients with clinically stable brain metastases or leptomeningeal disease (previously treated or untreated) are eligible. Patients in expansion cohort A must have at least one untreated CNS lesion
Women who are breastfeeding or pregnant.
Any evidence of clinically active interstitial lung disease.