Gefitinib therapy in advanced bronchioloalveolar carcinoma: Southwest Oncology Group study S0126

被引:120
作者
West, HL
Franklin, WA
Mccoy, J
Gumerlock, PH
Vance, R
Lau, DHM
Chansky, K
Crowley, JJ
Gandara, DR
机构
[1] SW Oncol Grp, Ctr Stat, Seattle, WA USA
[2] Puget Sound Oncol Consortium, Swedish Canc Inst, Seattle, WA USA
[3] Univ Colorado, Denver, CO 80202 USA
[4] Univ Calif Davis, Sacramento, CA 95817 USA
[5] Univ Mississippi, Med Ctr, Jackson, MS 39216 USA
关键词
D O I
10.1200/JCO.2005.04.9890
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Advanced bronchioloalveolar carcinoma (BAC) is a distinct subtype of non-small-cell lung cancer (NSCLC) for which there is currently no optimal therapy. Based on preclinical and clinical data suggesting relevance of the epidermal growth factor receptor (EGFR) axis in BAC, the Southwest Oncology Group initiated a phase II trial (S0126) to evaluate the EGFR tyrosine kinase inhibitor gefitinib in chemotherapy-naive and chemotherapy-pretreated patients with advanced BAC. Methods A total of 136 eligible and assessable patients (101 untreated, 35 previously treated) received gefitinib 500 mg daily until progression or prohibitive toxicity. Results The median age was 68.0 years (range, 34.3 to 88.6); 51% were female; 89% had a performance status (PS) of 0% or 1% and 11% had a PS of 2. The Response Evaluation Criteria in Solid Tumors response rate was 17%, with 6% complete responses (CRs) among 69 previously untreated patients with measurable disease, and 9% with no CRs among 22 pretreated patients. Median survival was 13 months for both chemo-naive (95% CI, 8 to 18) and previously treated patients (95% CI, 6 to 17). Overall survival at 3 years was 23% (95% CI, 14% to 32%). Toxicity consisted mainly of rash and diarrhea, but 2% of patients died of presumed interstitial lung disease. Exploratory subset analyses revealed improved survival among women (P = .031), patients developing a rash (P = .003), never-smokers (P = .061), and patients with a PS of 0 or 1 (P = .015). Conclusion Gefitinib is an active agent in advanced stage BAC. Several subsets demonstrate significantly improved clinical outcomes.
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页码:1807 / 1813
页数:7
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