Wood-smoke exposure as a response and survival predictor in erlotinib-treated non-small cell lung cancer patients - An open lobel phase II study

被引:27
作者
Arrieta, Oscar [1 ,2 ]
Martinez-Barrera, Luis
Trevino, Sergio [3 ]
Guzman, Enrique
Castillo-Gonzalez, Patricia
Angel Rios-Trejo, Miguel [2 ]
Flores-Estrada, Diana [1 ]
Tellez, Eduardo [4 ]
Gonzalez, Cesar [5 ]
de la Cruz Vargas, Johny [6 ]
Gonzalez-De la Rosa, Claudia Haydee [7 ]
Hernandez-Pedro, Norma [1 ]
Morales-Barrera, Rafael [1 ]
De la Garza, Jaime [1 ]
机构
[1] Inst Nacl Cancerol, Dept Med Oncol, Tlalpan 14080, Mexico
[2] Univ Nacl Autonoma Mexico, Mexico City 04510, DF, Mexico
[3] Univ Monterrey, Monterrey, Nuevo Leon, Mexico
[4] Inst Seguridad Social Trabajadores Estado, Dept Med Oncol, Puebla, Mexico
[5] Hosp Christ Muguerza, Monterrey, Nuevo Leon, Mexico
[6] Grp Oncol Acapulco, Guerrero, Mexico
[7] UAM Cuajimalpa, Dept Nat Sci, Mexico City, DF, Mexico
关键词
erlotinib; non-small cell cancer; response predictor; survival predictor; wood-smoke eposure;
D O I
10.1097/JTO.0b013e31818026f6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Erlotinib, a tyrosine kinase inhibitor, has improved survival and quality of life in patients with non-small cell lung cancer (NSCLC) after first- or second-line chemotherapy. Asian Origin, adenocarcinoma histology, female gender, lack of tobacco use, and expression of epidermal growth factor receptor are significant independent predictors of response to Erlotinib. Although tobacco Use is considered a major cause of NSCLC. other risk factors such as wood-smoke exposure (WSE) are associated. Almost 3 billion people worldwide rely oil solid fuels Lis their primary source of domestic energy for cooking and heating. Methods: In this Study, 150 consecutive unselected patients with histologically proven NSCLC with progression after prior first- or second-line chemotherapy and/or poor performance status were treated with Erlotinib 150 mg/d. Clinical and pathologic characteristics were associated with response. Results: Overall response to Erlotinib was observed in 51 patients [34%; 95% confidence interval {95%, CI}, 29.9-37.6]. In multivariate analysis, clinical features associated with response to Erlotinib were adenocarcinoma (35 versus 20%; p=0.05) and WSE (83 versus 13%; p < 0.001). Factors associated with longer progression-free survival ill COX analysis included adenocarcinoma (7.9 versus 2.3 months; p = 0.009), female gender (8.4 versus 5.3 months; p=0.04), and WSE (17.6 versus 5.3 months; p = 0.006). Conclusions: WSE is associated with better response to Erlotinib and improved progression-free survival in patients with NSCLC. Additional studies in epidermal growth factor receptor signaling pathway in WSE-associated NSCLC are warranted.
引用
收藏
页码:887 / 893
页数:7
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