Systemic Therapy for Small Cell Lung Cancer

被引:13
作者
Levy, Benjamin [1 ]
Saxena, Ashish [2 ]
Schneider, Bryan J. [2 ]
机构
[1] Weill Cornell Med Coll, Dept Hematol Oncol, Dept Internal Med, Beth Israel Comprehens Canc Ctr, New York, NY 10021 USA
[2] Weill Cornell Med Coll, Div Hematol Oncol, Dept Internal Med, New York, NY 10021 USA
来源
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK | 2013年 / 11卷 / 07期
关键词
PHASE-III TRIAL; COLONY-STIMULATING FACTOR; RECOMBINANT INTERFERON-GAMMA; CISPLATIN PLUS ETOPOSIDE; MAINTENANCE THERAPY; DOSE-INTENSITY; COMBINATION CHEMOTHERAPY; INDUCTION CHEMOTHERAPY; EUROPEAN-ORGANIZATION; RESPONDING PATIENTS;
D O I
10.6004/jnccn.2013.0100
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Small cell lung cancer is an aggressive tumor characterized by genetic complexity, rapid doubling time, and early development of disseminated disease. Unfortunately, few chemotherapeutic advances have been made in the treatment of extensive-stage disease, and cisplatin/etoposide has remained the standard of care for more than 30 years. Other regimens with comparable efficacy include cisplatin/irinotecan and carboplatin/etoposide. Each of these combinations is associated with a different toxicity profile that must be considered when selecting an initial regimen. Several strategies, including maintenance chemotherapy, 3-drug combinations, alternating combination chemotherapy regimens, and high-dose chemotherapy, have consistently failed to demonstrate improvements in survival when compared with 4 to 6 cycles of platinum doublets. Several options are available for patients who experience progression during or relapse after induction therapy, although topotecan is the only FDA-approved agent for second-line treatment. Recently, scientific efforts have identified potentially actionable genetic alterations in small cell tumors that may lead to the development of effective, targeted therapies.
引用
收藏
页码:780 / 787
页数:8
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