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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Carboplatin | Small molecule | 6 unknown | — |
| Subject | Erlotinib | Small molecule | 150 mg | Oral |
| Comparator | Paclitaxel | Small molecule | 200 mg/m2 | Intravenous |