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小细胞肺癌的个体化治疗

Personalized Therapy of Small Cell Lung Cancer.

作者信息

Schneider Bryan J, Kalemkerian Gregory P

机构信息

Division of Hematology/Oncology, University of Michigan, C411 Med Inn-SPC 5848, 1500 E. Medical Center Dr., Ann Arbor, MI, 48109-5848, USA.

Division of Hematology/Oncology, University of Michigan, C350 Med Inn-SPC 5848, 1500 E. Medical Center Dr., Ann Arbor, MI, 48109-5848, USA.

出版信息

Adv Exp Med Biol. 2016;890:149-74. doi: 10.1007/978-3-319-24932-2_9.

Abstract

Small cell lung cancer (SCLC) is an aggressive, poorly differentiated neuroendocrine carcinoma with distinct clinical, pathological and molecular characteristics. Despite robust responses to initial chemotherapy and radiation, the prognosis of patients with SCLC remains poor with an overall 5-year survival rate of less than 10 %. Despite the fact that numerous molecularly targeted approaches have thus far failed to demonstrate clinical utility in SCLC, further advances will rely on better definition of the biological pathways that drive survival, proliferation and metastasis. Recent next-generation, molecular profiling studies have identified many new therapeutic targets in SCLC, as well as extreme genomic instability which explains the high degree of resistance. A wide variety of anti-angiogenic agents, growth factor inhibitors, pro-apoptotic agents, and epigenetic modulators have been evaluated in SCLC and many studies of these strategies are on-going. Perhaps the most promising approaches involve agents targeting cancer stem cell pathways and immunomodulatory drugs that interfere with the PD1 and CTLA-4 pathways. SCLC offers many barriers to the development of successful therapy, including limited tumor samples, inadequate preclinical models, high mutational burden, and aggressive tumor growth which impairs functional status and hampers enrollment on clinical trials.

摘要

小细胞肺癌(SCLC)是一种侵袭性强、低分化的神经内分泌癌,具有独特的临床、病理和分子特征。尽管对初始化疗和放疗反应强烈,但SCLC患者的预后仍然很差,总体5年生存率不到10%。尽管迄今为止众多分子靶向治疗方法在SCLC中未能显示出临床应用价值,但进一步的进展将依赖于对驱动生存、增殖和转移的生物学途径的更清晰定义。最近的新一代分子谱分析研究已经在SCLC中确定了许多新的治疗靶点,以及解释高度耐药性的极端基因组不稳定性。多种抗血管生成剂、生长因子抑制剂、促凋亡剂和表观遗传调节剂已在SCLC中进行了评估,并且许多关于这些策略的研究正在进行中。也许最有前景的方法涉及靶向癌症干细胞途径的药物和干扰PD1和CTLA-4途径的免疫调节药物。SCLC为成功治疗的发展带来了许多障碍,包括肿瘤样本有限、临床前模型不足、高突变负荷以及侵袭性肿瘤生长,这损害了功能状态并阻碍了临床试验的入组。

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