New Advances in the Second-Line Treatment of Small Cell Lung Cancer

被引:95
作者
Hurwitz, Jane L. [2 ]
McCoy, Francis
Scullin, Paula [2 ]
Fennell, Dean A. [1 ,2 ]
机构
[1] Queens Univ Belfast, Ctr Canc Res & Cell Biol, Thorac Oncol Res Grp, Belfast BT9 7BL, Antrim, North Ireland
[2] No Ireland Canc Ctr, Belfast, Antrim, North Ireland
关键词
Small cell lung cancer; Relapsed; Chemotherapy; BCL-2; Apoptosis; PHASE-II TRIAL; BCL-2 ANTISENSE OLIGONUCLEOTIDE; BH3 MIMETIC ABT-737; INTRAVENOUS TOPOTECAN; APOPTOSIS; CISPLATIN; CHEMOTHERAPY; ETOPOSIDE; CARBOPLATIN; RESISTANCE;
D O I
10.1634/theoncologist.2009-0026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is the leading cause of cancer-related death in the U. K., with small cell histology accounting for 15%-20% of cases. Small cell lung cancer (SCLC) is initially a chemosensitive disease, but relapse is common, and in this group of patients it remains a rapidly lethal disease with a particularly poor prognosis. The choice of second-line chemotherapy for patients with relapsed SCLC has been an area of difficulty for oncologists, and until recently there was no randomized evidence for its use over best supportive care (BSC). Topotecan is currently the only drug licensed in Europe and the U. S. for this indication, having been shown in a phase III trial to lead to longer overall survival and better quality of life than with BSC. In this article, we review the current evidence for the use of secondline cytotoxic therapy and also the emerging role of novel agents and targeted therapies in this setting. In particular, we explore the role of the Bcl-2 protein family, which are key regulators of mitochondrial apoptosis and are implicated in resistance to anticancer therapies. SCLC overexpresses antiapoptotic members of the Bcl-2 family in similar to 80% of cases. Several Bcl-2 inhibitors, including obatoclax, are currently entering clinical trials in SCLC and are an exciting area of drug development in the relapsed setting. The Oncologist 2009; 14: 986-994
引用
收藏
页码:986 / 994
页数:9
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