Efficacy and safety of gefitinib in chemonaive patients with advanced non-small cell lung cancer treated in an Expanded Access Program

被引:7
作者
Govindan, Ramaswamy
Natale, Ronald
Wade, James
Herbst, Roy
Krebs, Annetta
Reiling, Richard
Hensing, Thomas
Wozniak, Antoinette
Belani, Chandra P.
Kelly, Karen
Ochs, Judith
机构
[1] Washington Univ, Sch Med, Dept Med Oncol, St Louis, MO 63110 USA
[2] Cedars Sinai Comprehens Canc Ctr, Los Angeles, CA 90048 USA
[3] Canc Care Specialists Cent Illinois, Decatur, GA USA
[4] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[5] AstraZeneca Pharmaceut LP, Wilmington, DE 19850 USA
[6] Presbyterian Ctr Canc Res, Charlotte, NC 28204 USA
[7] Evanston Hosp Corp, Kellogg Canc Ctr, Feinberg Sch Med, Evanston, IL 60201 USA
[8] Wayne State Univ, Harper Hosp, Karmanos Canc Inst, Detroit, MI 48201 USA
[9] Hillman Canc Ctr, Pittsburgh, PA 15232 USA
[10] Univ Colorado, Hlth Sci Ctr, Denver, CO 80262 USA
关键词
gefitinib; non-small cell lung cancer; chemonaive; EGFR-TKI; expanded access program; molecular targeted therapy;
D O I
10.1016/j.lungcan.2006.04.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemotherapy (CT) is recommended in numerous clinical guidelines for advanced non-small cell lung cancer (NSCLC) and offers improved survival over best supportive care. However, many patients with advanced NSCLC never receive CT because of advanced age, poor performance status, comorbidities, or patient refusal. The epidermal growth factor receptor tyrosine kinase inhibitor gefitinib has shown antitumor activity and a favorable toxicity profile in pretreated patients with recurrent advanced NSCLC and was made available in a worldwide Expanded Access Program (EAP) to >37,000 patients who did not respond to standard treatment or were ineligible for or refused CT A retrospective chart review of 1671 consecutive patients enrolled at 11 sites in the US arm of the EAP identified 198 patients with advanced NSCLC who had not received previous CT All patients were treated with gefitinib 250 mg/d until treatment failure or toxicity occurred. Patients were treated for a mean of 4.7 months. The most common adverse events were diarrhea (31.3%) and rash (31.3%). Complete and partial response rates were 0.7 and 5.6%, respectively, and 40.6% had stable disease. Median survival was 6 months, and estimated 1-year survival was 29.7%. The majority of patients did not receive subsequent (C) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:331 / 337
页数:7
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