drugset / Trial / NCT00085839

Erlotinib vs. Standard Chemotherapy in Patients With Advanced Non-small Cell Lung Cancer (NSCLC) and Eastern Cooperative Oncology Group (ECOG)Performance Status (PS) 2

NCT00085839 ↗

Phase 2 Completed 103 enrolled OSI Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this noncomparative study is to obtain preliminary estimates of the efficacy of erlotinib and standard chemotherapy in patients with advanced, previously untreated nonsmall cell lung cancer (NSCLC) and an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 2. The study will also evaluate the safety of single-agent erlotinib in this patient population.

Timeline

Start
2004-02
Primary completion
2007-03
Completion
2007-03

Outcome

Missed primary endpoint

paper Median PFS was 1.9 months in the erlotinib arm and 3.5 months in the chemotherapy arm (hazard ratio [HR] = 1.45; 95% CI, 0.98 to 2.15; P = .06). PMID 18281658 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Carboplatin Small molecule 6 unknown —
Subject Erlotinib Small molecule 150 mg Oral
Comparator Paclitaxel Small molecule 200 mg/m2 Intravenous