Current and emerging therapies for patients with advanced non-small-cell lung cancer

被引:10
作者
Sheth, Sheetal [1 ]
机构
[1] US Oncol, The Woodlands, TX 77380 USA
关键词
Antineoplastic agents; Bevacizumab; Cetuximab; Cisplatin; Combined therapy; Docetaxel; Erlotinib; Gemcitabine; Genetics; Lung neoplasms; Pemetrexed; Site of action; Toxicity; Vandetanib; PHASE-III TRIAL; CHEMOTHERAPY-NAIVE PATIENTS; CARBOPLATIN; PACLITAXEL;
D O I
10.2146/ajhp090457
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose. To review recent clinical trials that have examined new options for the treatment of non-small-cell lung cancer (NSCLC) and to review the importance of tumor histology and genetics in the selection of therapy. Summary. Targeted biological agents have been evaluated for use in patients with NSCLC. In a recent study, treatment with cetuximab plus chemotherapy led to significant improvement in overall survival (OS) in patients with advanced NSCLC. A Phase III, noninferiority, randomized study evaluating first-line therapy in patients with stage IIIb or IV NSCLC demonstrated that the combination of cisplatin and pemetrexed was noninferior to cisplatin and gemcitabine in improving OS and other clinical outcomes. In this study, the combination of pemetrexed and cisplatin was effective in patients with nonsquamous disease, whereas the combination of cisplatin and gemcitabine was effective in improving progression-free survival (PFS) in patients with squamous cell carcinoma. Clinical trials of maintenance therapy presented at the 2009 annual meeting of the American Society of Clinical Oncology reported significant benefit of pemetrexed in patients with nonsquamous tumor histology, and of erlotinib in patients with squamous and nonsquamous histology. For second-line therapy, studies of the investigational tyrosine kinase inhibitor, vandetanib, failed to demonstrate improved OS with vandetanib in combination with docetaxel or pemetrexed, or in direct comparison with erlotinib. In another study, the addition of bevacizumab to erlotinib for second-line treatment of NSCLC did not result in greater OS than erlotinib alone. Conclusion. New treatment strategies are needed to improve clinical outcomes for patients with advanced NSCLC. The introduction of new agents with improved tolerability profiles has led to interest in long-term maintenance therapy in this patient population. Clinical trials suggest that tumor histology and genetics should be considered when selecting treatments for these patients.
引用
收藏
页码:S9 / S14
页数:6
相关论文
共 19 条
[1]   A phase I trial of aprinocarsen (ISIS 3521/LY900003), an antisense inhibitor of protein kinase C-α administered as a 24-hour weekly infusion schedule in patients with advanced cancer [J].
Advani, R ;
Lum, BL ;
Fisher, GA ;
Halsey, J ;
Geary, RS ;
Holmlund, JT ;
Kwoh, TJ ;
Dorr, FA ;
Sikic, BI .
INVESTIGATIONAL NEW DRUGS, 2005, 23 (05) :467-477
[2]  
[Anonymous], National Comprehensive Cancer Network Compendium
[3]  
BELANI CP, 2009, 45 AM SOC CLIN ONC A
[4]   Phase III trial comparing carboplatin, paclitaxel, and bexarotene with carboplatin and paclitaxel in chemotherapy-naive patients with advanced or metastatic non-small-cell lung cancer: SPIRIT II [J].
Blumenschein, George R., Jr. ;
Khuri, Fadlo R. ;
von Pawel, Joachim ;
Gatzemeier, Ulrich ;
Miller, Wilson H., Jr. ;
Jotte, Robert M. ;
Le Treut, Jacques ;
Sun, Show-Li ;
Zhang, Jinkun K. ;
Dziewanowska, Zofia E. ;
Negro-Vilar, Andres .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (11) :1879-1885
[5]  
CAPPUZZO F, 2009, 45 AM SOC CLIN ONC A
[6]  
CIULEANU TE, 2008, 44 AM SOC CLIN ONC A
[7]  
DEBOER R, 2009, 45 AM SOC CLIN ONC A
[8]  
*EL LILL CO, 2009, AL PEM PRESCR INF
[9]  
Hainsworth J., 2008, 2008 CHIC MULT S THO
[10]   TRIBUTE: A phase III trial of erlotinib hydrochloride (OSI-774) combined with carboplatin and paclitaxel chemotherapy in advanced non-small-cell lung cancer [J].
Herbst, RS ;
Prager, D ;
Hermann, R ;
Fehrenbacher, L ;
Johnson, BE ;
Sandler, A ;
Kris, MG ;
Tran, HT ;
Klein, P ;
Li, X ;
Ramies, D ;
Johnson, DH ;
Miller, VA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :5892-5899