TY - JOUR
T1 - Bortezomib for patients with advanced-stage bronchioloalveolar carcinoma
T2 - A California cancer consortium phase II study (NCI 7003)
AU - Ramalingam, Suresh S.
AU - Davies, Angela M.
AU - Longmate, Jeffrey
AU - Edelman, Martin J.
AU - Lara, Primo N.
AU - Vokes, Everett E.
AU - Villalona-Calero, Miguel
AU - Gitlitz, Barbara
AU - Reckamp, Karen
AU - Salgia, Ravi
AU - Wright, John J.
AU - Belani, Chandra P.
AU - Gandara, David R.
N1 - Funding Information:
Supported by NCI NO1-CM-62209 (California Cancer Consortium), NO1-CM-62201 (University of Chicago Consortium), NO1-CM-62208 (Southeast Phase 2 Consortium), and NO1-CM-62207 (Ohio State University).
Funding Information:
Disclosure: Dr. Lara has served as a consultant and received research funding from Millennium Pharmaceuticals. The other authors have no conflicts of interest.
PY - 2011/10
Y1 - 2011/10
N2 - Background: Bronchioloalveolar carcinoma (BAC), a subtype of non-small cell lung cancer, is a difficult disease to treat with low response rates with cytotoxic chemotherapy. Bortezomib, a proteasome inhibitor, has demonstrated objective responses in patients with BAC in early-phase clinical trials. We conducted a phase II study of bortezomib in patients with advanced-stage BAC. Methods: Patients with advanced BAC, adenocarcinoma with BAC features or BAC with adenocarcinoma features, and less than two prior regimens were eligible. Prior epidermal growth factor receptor (EGFR) inhibitor therapy was allowed. Bortezomib was administered intravenously at 1.6 mg/m on days 1 and 8 of every 21-day cycle until disease progression or unacceptable toxicity. The primary end point was response rate. The Simon two-stage design was used. Results: Forty-two patients were enrolled, and the study was halted early for slow accrual. Patient characteristics were female 55%, median age 68 years, and Eastern Cooperative Oncology Group performance status of 0 and 1 in 31 and 11 patients, respectively. Twenty-six (62%) patients had received prior therapy with an EGFR inhibitor. A median of four cycles of therapy were administered. Objective responses were noted in 5%, whereas 57% had disease stabilization. The median progression-free survival and overall survival were 5.5 and 13.6 months, respectively. Grade 3 diarrhea and fatigue were noted in three and five patients, respectively. Conclusions: Bortezomib is tolerated well and is associated with modest anticancer activity in patients with advanced BAC, including patients who progressed on EGFR inhibitor therapy.
AB - Background: Bronchioloalveolar carcinoma (BAC), a subtype of non-small cell lung cancer, is a difficult disease to treat with low response rates with cytotoxic chemotherapy. Bortezomib, a proteasome inhibitor, has demonstrated objective responses in patients with BAC in early-phase clinical trials. We conducted a phase II study of bortezomib in patients with advanced-stage BAC. Methods: Patients with advanced BAC, adenocarcinoma with BAC features or BAC with adenocarcinoma features, and less than two prior regimens were eligible. Prior epidermal growth factor receptor (EGFR) inhibitor therapy was allowed. Bortezomib was administered intravenously at 1.6 mg/m on days 1 and 8 of every 21-day cycle until disease progression or unacceptable toxicity. The primary end point was response rate. The Simon two-stage design was used. Results: Forty-two patients were enrolled, and the study was halted early for slow accrual. Patient characteristics were female 55%, median age 68 years, and Eastern Cooperative Oncology Group performance status of 0 and 1 in 31 and 11 patients, respectively. Twenty-six (62%) patients had received prior therapy with an EGFR inhibitor. A median of four cycles of therapy were administered. Objective responses were noted in 5%, whereas 57% had disease stabilization. The median progression-free survival and overall survival were 5.5 and 13.6 months, respectively. Grade 3 diarrhea and fatigue were noted in three and five patients, respectively. Conclusions: Bortezomib is tolerated well and is associated with modest anticancer activity in patients with advanced BAC, including patients who progressed on EGFR inhibitor therapy.
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U2 - 10.1097/JTO.0b013e318225924c
DO - 10.1097/JTO.0b013e318225924c
M3 - Article
C2 - 21716143
AN - SCOPUS:80052962938
SN - 1556-0864
VL - 6
SP - 1741
EP - 1745
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 10
ER -