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ABSTRACT: Introduction
This phase I trial was conducted to determine the safety, maximum tolerated dose (MTD)/recommended phase II dose, and efficacy of crizotinib plus erlotinib in patients with advanced NSCLC.Methods
Patients with NSCLC and an Eastern Cooperative Oncology Group performance status of 0 to 2 after failure of one or two prior chemotherapy regimens were eligible. Erlotinib, 100 mg, was given continuously once daily starting between day -14 and -7; crizotinib, 200 mg twice daily (dose level 1) or 150 mg twice daily (dose level -1), was added continuously beginning on day 1 of treatment cycle 1. Potential pharmacokinetic interactions between crizotinib and erlotinib were evaluated.Results
Twenty-seven patients received treatment; 26 received crizotinib plus erlot
SUBMITTER: Ou SI
PROVIDER: S-EPMC7249761 | biostudies-literature | 2017 Jan
REPOSITORIES: biostudies-literature