Southwest oncology group phase II trial (S0341) of erlotinib (OSI-774) in patients with advanced non-small cell lung cancer and a performance status of 2

作者：Hesketh Paul J^*; Chansky Kari; Wozniak Antoinette J; Hirsch Fred R; Spreafico Anna; Moon James; Mack Philip C; Marchello Benjamin T; Franklin Wilbur A; Crowley John J; Gandara David R

来源：Journal of Thoracic Oncology, 2008, 3(9): 1026-1031.

DOI：10.1097/JTO.0b013e318183aa1f

Put-pose: This phase 11 Study (S0341) evaluated file efficacy and tolerability of single-agent erlotinib in unselected chemotherapynaive patients with advanced non-small cell lung cancer (NSCLC) and a performance status (PS) of 2. Exploratory analyses of a number of biomarkers relating to epidermal growth factor receptor pathway activation were also performed.
Patients and Methods: Patients with stage IIIB (pleural effusion) Or stage IV NSCLC with a PS of 2 and no prior chemotherapy or biologic treatment for NSCLC received erlotinib 150 mg daily.
Results: A total of 81 patients entered the Study; 76 were assessable. One complete and 5 partial responses were noted for all overall response rate of 8% (95% Cl 3%-16%). Stable disease (SD) was seen in 26 patients (34%) resulting in a disease control rate (DCR = CR/PR/SD) of 42%. Progression free and median survival were 2.1 months (95% Cl 1.5-3.1 and 5 months (95% CI 3.6-7.2), espectively. One-year survival was, 24% (95% Cl 15%-34%). Although treatment was generally well tolerated, grade 3 to 4 toxicity Was reported in 30 patients (40%), including fatigue (16%). rash (9%), diarrhea (7%), and anorexia (7%). There was one possible treatment related death (pneumonitis).
Conclusions: In chemotherapy-naive patients with advanced NSCLC and a PS of 2, single agent erlotinib resulted in an acceptable but significant level of treatment-related side effects. With an overall DCR of 42% and median survival of 5 months, results are comparable to those achieved with chemotherapy in this population. Development of all epidermal growth factor receptor-directed biomarker selection strategy may optimize use of erlotinib in PS 2 patients.

• 出版日期2008-9