Skip to main navigation Skip to search Skip to main content

Phase I Results from a Study of Crizotinib in Combination with Erlotinib in Patients with Advanced Nonsquamous Non–Small Cell Lung Cancer

  • Sai Hong Ignatius Ou
  • , Ramaswamy Govindan
  • , Keith D. Eaton
  • , Gregory A. Otterson
  • , Martin E. Gutierrez
  • , Alain C. Mita
  • , Athanassios Argiris
  • , Nicoletta M. Brega
  • , Tiziana Usari
  • , Weiwei Tan
  • , Steffan N. Ho
  • , Francisco Robert
  • University of California at Irvine
  • Washington University St. Louis
  • Seattle Cancer Care Alliance
  • Ohio State University
  • University of Texas Health Science Center at San Antonio
  • Pfizer
  • Department of Veterans Affairs
  • University of Alabama at Birmingham

Research output: Contribution to journal › Article › peer-review

51 Scopus citations

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 erlotinib. Frequent adverse events were diarrhea, rash, decreased appetite, and fatigue. Dose-limiting toxicities were dehydration, diarrhea, dry eye, dysphagia, dyspepsia, esophagitis and vomiting. The MTD was crizotinib, 150 mg twice daily, with erlotinib, 100 mg once daily. Crizotinib increased the erlotinib area under the concentration-time curve 1.5-fold (dose level −1) and 1.8-fold (dose level 1). The plasma level of crizotinib appeared to be unaffected by coadministration of erlotinib. Two patients whose tumors harbored activating EGFR mutations achieved confirmed partial responses, one at each crizotinib dose level. Conclusions The MTD of the combination of crizotinib and erlotinib in patients with advanced NSCLC was crizotinib, 150 mg twice daily, with erlotinib, 100 mg once daily, which is less than the approved dose of either agent. The phase II portion of the study was not initiated.

Original languageEnglish
Pages (from-to)145-151
Number of pages7
JournalJournal of Thoracic Oncology
Volume12
Issue number1
DOIs
StatePublished - 1 Jan 2017

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Crizotinib
  • EGFR inhibitor
  • Erlotinib
  • MET inhibitor
  • Phase I combination trial

Fingerprint

Dive into the research topics of 'Phase I Results from a Study of Crizotinib in Combination with Erlotinib in Patients with Advanced Nonsquamous Non–Small Cell Lung Cancer'. Together they form a unique fingerprint.

Cite this