Potential role of molecularly targeted therapy in the management of advanced nonsmall cell lung carcinoma in the elderly

被引:8
作者
Gridelli, C
Massarelli, E
Maione, P
Rossi, A
Herbst, RS
Onn, A
Ciardiello, F
机构
[1] San Giuseppe Moscati Hosp, Div Med Oncol, I-83100 Avellino, Italy
[2] Univ Texas, MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Pulm Med, Houston, TX 77030 USA
[4] Univ Naples 2, Sch Med, Dept Clin & Expt Med, Naples, Italy
关键词
targeted therapy; chemotherapy; elderly; advanced nonsmall cell lung carcinoma;
D O I
10.1002/cncr.20572
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. More than 50% of all lung carcinoma cases are diagnosed in patients age >65 years, and approximately 30% are diagnosed in patients age >70 years. Elderly patients do not tolerate chemotherapy as well as their younger counterparts do, primarily because of the increased prevalence of comorbid conditions and organ failure. Thus, at present, the majority of elderly patients with malignant disease do not receive aggressive chemotherapy. For such elderly patients, alternatives to conventional chemotherapy, such as novel molecularly targeted therapy regimens, are of interest. Methods. The current review summarizes contemporary approaches to and recent advances in the treatment of elderly patients with nonsmall cell lung carcinoma (NSCLC) and offers perspectives on the future of molecularly targeted therapy in this population. Inhibitors of epidermal growth factor receptor, vascular endothelial growth factor, and cyclooxygenase-2 are discussed in the current report, with such inhibitors being, in our opinion, among the best candidates for clinical development in the setting of interest. Results. Novel biologic agents with putative activity against advanced NSCLC are at various stages of clinical development. Some of these agents have yielded benefits in terms of disease-related symptom reduction quality of life and survival. For elderly patients, the potential advantages of such agents include improved tolerability compared with conventional chemotherapy. This feature also makes these novel agents attractive alternatives for younger patients who cannot tolerate or are reluctant to receive conventional chemotherapy. Conclusions. Current studies are investigating the safety and efficacy of these novel biologic agents administered alone, in combination with other noncytotoxic agents, and in combination with conventional chemotherapy. These studies will help elucidate the role of targeted therapy in the management of elderly patients with advanced NSCLC.
引用
收藏
页码:1733 / 1744
页数:12
相关论文
共 89 条
[61]   Efficacy of gefitinib, an inhibitor of the epidermal growth factor receptor tyrosine kinase, in symptomatic patients with non-small cell lung cancer - A randomized trial [J].
Kris, MG ;
Natale, RB ;
Herbst, RS ;
Lynch, TJ ;
Prager, D ;
Belani, CP ;
Schiller, JH ;
Kelly, K ;
Spiridonidis, H ;
Sandler, A ;
Albain, KS ;
Cella, D ;
Wolf, MK ;
Averbuch, SD ;
Ochs, JJ ;
Kay, AC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (16) :2149-2158
[62]   Cisplatin-based combination chemotherapy for elderly patients with non-small-cell lung cancer [J].
Kubota, K ;
Furuse, K ;
Kawahara, M ;
Kodama, N ;
Ogawara, M ;
Takada, M ;
Masuda, N ;
Negoro, S ;
Matsui, K ;
Takifuji, N ;
Kudoh, S ;
Kusunoki, Y ;
Fukuoka, M .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1997, 40 (06) :469-474
[63]  
Langer CJ, 2002, JNCI-J NATL CANCER I, V94, P173
[64]   Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib [J].
Lynch, TJ ;
Bell, DW ;
Sordella, R ;
Gurubhagavatula, S ;
Okimoto, RA ;
Brannigan, BW ;
Harris, PL ;
Haserlat, SM ;
Supko, JG ;
Haluska, FG ;
Louis, DN ;
Christiani, DC ;
Settleman, J ;
Haber, DA .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (21) :2129-2139
[65]  
MADRONAL C, 2002, P AN M AM SOC CLIN, V21, pB221
[66]   Status of epidermal growth factor receptor antagonists in the biology and treatment of cancer [J].
Mendelsohn, J ;
Baselga, J .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (14) :2787-2799
[67]  
Millauer B, 1996, CANCER RES, V56, P1615
[68]  
MILLER VA, 2003, P AN M AM SOC CLIN, V22, P619
[69]   Cooperative inhibitory effect of ZD1839 (Iressa) in combination with trastuzumab (Herceptin) on human breast cancer cell growth [J].
Normanno, N ;
Campiglio, M ;
De Luca, A ;
Somenzi, G ;
Maiello, M ;
Ciardiello, F ;
Gianni, L ;
Salomon, DS ;
Menard, S .
ANNALS OF ONCOLOGY, 2002, 13 (01) :65-72
[70]   EGFR mutations in lung cancer:: Correlation with clinical response to gefitinib therapy [J].
Paez, JG ;
Jänne, PA ;
Lee, JC ;
Tracy, S ;
Greulich, H ;
Gabriel, S ;
Herman, P ;
Kaye, FJ ;
Lindeman, N ;
Boggon, TJ ;
Naoki, K ;
Sasaki, H ;
Fujii, Y ;
Eck, MJ ;
Sellers, WR ;
Johnson, BE ;
Meyerson, M .
SCIENCE, 2004, 304 (5676) :1497-1500