TY - JOUR
T1 - Targeted and cytotoxic therapy in coordinated sequence (TACTICS)
T2 - Erlotinib, bevacizumab, and standard chemotherapy for nonsmall-cell lung cancer, a phase II trial
AU - Cohen, Ezra E.W.
AU - Subramanian, Janakiraman
AU - Gao, Feng
AU - Szeto, Livia
AU - Kozloff, Mark
AU - Faoro, Leonardo
AU - Karrison, Theodore
AU - Salgia, Ravi
AU - Govindan, Ramaswamy
AU - Vokes, Everett E.
PY - 2012/3
Y1 - 2012/3
N2 - Background: This trial focused on optimally combining existing targeted therapies and cytotoxic chemotherapy in the treatment of unselected patients with advanced nonsmall-cell lung cancer (NSCLC). Methods: Patients with previously untreated advanced-stage nonsquamous NSCLC were eligible for this trial. In module A, patients received up to 4 cycles of erlotinib 150 mg daily and bevacizumab 15 mg/kg every 3 weeks. Patients then received carboplatin (AUC = 6), paclitaxel 200 mg/m2, and bevacizumab 15 mg/kg for 4 cycles in module B. Patients who did not have progressive disease in module A received maintenance erlotinib 150 mg daily and bevacizumab 15 mg/kg every 3 weeks in module C. Results: Forty-eight patients were enrolled in this multicenter phase II trial. Most patients were male (62.5%) and white (77.1%) with stage IV disease (93.8%) and adenocarcinoma histologic type (66.7%). The overall response rate in module A was 10.4%, in module B it was 15.1%, and in module C it was 5.5%. The study achieved its primary endpoint, with a nonprogression rate of 45.8% in module A. The median overall survival (OS) was 12.6 months. Conclusion: The novel systemic therapy regimen is feasible in patients with advanced NSCLC. However there is no further role for developing this regimen in unselected patients with NSCLC.
AB - Background: This trial focused on optimally combining existing targeted therapies and cytotoxic chemotherapy in the treatment of unselected patients with advanced nonsmall-cell lung cancer (NSCLC). Methods: Patients with previously untreated advanced-stage nonsquamous NSCLC were eligible for this trial. In module A, patients received up to 4 cycles of erlotinib 150 mg daily and bevacizumab 15 mg/kg every 3 weeks. Patients then received carboplatin (AUC = 6), paclitaxel 200 mg/m2, and bevacizumab 15 mg/kg for 4 cycles in module B. Patients who did not have progressive disease in module A received maintenance erlotinib 150 mg daily and bevacizumab 15 mg/kg every 3 weeks in module C. Results: Forty-eight patients were enrolled in this multicenter phase II trial. Most patients were male (62.5%) and white (77.1%) with stage IV disease (93.8%) and adenocarcinoma histologic type (66.7%). The overall response rate in module A was 10.4%, in module B it was 15.1%, and in module C it was 5.5%. The study achieved its primary endpoint, with a nonprogression rate of 45.8% in module A. The median overall survival (OS) was 12.6 months. Conclusion: The novel systemic therapy regimen is feasible in patients with advanced NSCLC. However there is no further role for developing this regimen in unselected patients with NSCLC.
KW - Bevacizumab
KW - EGFR TK mutation
KW - Erlotinib
KW - NSCLC advanced stage
UR - http://www.scopus.com/inward/record.url?scp=84857433962&partnerID=8YFLogxK
U2 - 10.1016/j.cllc.2011.10.001
DO - 10.1016/j.cllc.2011.10.001
M3 - Article
C2 - 22100149
AN - SCOPUS:84857433962
SN - 1525-7304
VL - 13
SP - 123
EP - 128
JO - Clinical Lung Cancer
JF - Clinical Lung Cancer
IS - 2
ER -