Rudin Charles M, Hann Christine L, Peacock Craig D, Watkins D Neil
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland 21231, USA.
J Natl Compr Canc Netw. 2008 Mar;6(3):315-22. doi: 10.6004/jnccn.2008.0026.
A diagnosis of small cell lung cancer (SCLC) today confers essentially the same terrible prognosis that it did 25 years ago, when common use of cisplatin-based chemotherapy began for this disease. In contrast to past decades of research on many other solid tumors, studies of combination chemotherapy using later generation cytotoxics and targeted kinase inhibitors have not had a significant impact on standard care for SCLC. The past few years have seen suggestions of incrementally improved outcomes using standard cytotoxics, including cisplatin-based combination studies of irinotecan and amrubicin by Japanese research consortia. Confirmatory phase III studies of these agents are ongoing in the United States. Antiangiogenic strategies are also of primary interest and are in late-phase testing. Several novel therapeutics, including high-potency small molecule inhibitors of Bcl-2 and the Hedgehog signaling pathway, and a recently discovered replication-competent picornavirus, have shown remarkable activity against SCLC in preclinical models and are currently in simultaneous phase I clinical development. Novel therapeutic approaches based on advances in understanding of the biology of SCLC have the potential to radically change the outlook for patients with this disease.
如今,小细胞肺癌(SCLC)的诊断所带来的预后与25年前基本相同,那时针对这种疾病开始普遍使用基于顺铂的化疗。与过去几十年对许多其他实体瘤的研究不同,使用新一代细胞毒性药物和靶向激酶抑制剂进行联合化疗的研究对SCLC的标准治疗并未产生重大影响。过去几年,有迹象表明使用标准细胞毒性药物可逐步改善治疗结果,包括日本研究团队进行的基于顺铂的伊立替康和氨柔比星联合研究。美国正在对这些药物进行验证性III期研究。抗血管生成策略也备受关注,正处于后期试验阶段。几种新型疗法,包括高效的Bcl-2小分子抑制剂和Hedgehog信号通路抑制剂,以及最近发现的一种具有复制能力的微小核糖核酸病毒,在临床前模型中已显示出对SCLC具有显著活性,目前正同时处于I期临床开发阶段。基于对SCLC生物学理解的进展而开发的新型治疗方法有可能从根本上改变这种疾病患者的前景。