Tsoukalas Nikolaos, Aravantinou-Fatorou Eleni, Baxevanos Panagiotis, Tolia Maria, Tsapakidis Konstantinos, Galanopoulos Michail, Liontos Michail, Kyrgias George
Department of Oncology, Veterans Hospital (NIMTS), Athens, Greece.
251 Air Force Hospital, Athens, Greece.
Ann Transl Med. 2018 Apr;6(8):145. doi: 10.21037/atm.2018.03.31.
Small cell lung cancer (SCLC) remains one of the most lethal malignancies and a major health riddle. The therapeutic options are limited. The combination of etoposide or irinotecan with platinum chemotherapy is the standard of care at any stage. The last decade systemic efforts have been done to reveal specific therapeutic targets for small cell lung carcinomas. In this review, we focus on the new therapeutic strategies of SCLC, including immune-related treatment that may change the prognosis of the disease. The main genetic mutations observed in SCLC are TP53 and RB1 mutations; however, it is well known that these molecules are not yet targetable. In recent years, research has revealed other frequent genetic alterations and activated signaling pathways that might be an effective treatment target. Loss of PTEN, activating PI3K mutations, inhibition of NOTCH pathway and aurora kinase activation are among them. Moreover, FDGFR1 amplification, activation of the Hedgehog pathway and repair-protein PARP1 seem to participate in SCLC tumorigenesis. These new findings have identified some interesting targets. Moreover, immunotherapy tries to find its place in the treatment of SCLC. Immune checkpoint inhibitors are under investigation in phase I to III clinical trials. We hope that in next years the treatment of SCLC patients will be improved with the administration of targeting therapy and the introduction of immunotherapy.
小细胞肺癌(SCLC)仍然是最致命的恶性肿瘤之一,也是一个重大的健康谜题。其治疗选择有限。依托泊苷或伊立替康与铂类化疗联合是任何阶段的标准治疗方案。在过去十年中,人们一直在进行系统性努力以揭示小细胞肺癌的特定治疗靶点。在本综述中,我们聚焦于SCLC的新治疗策略,包括可能改变疾病预后的免疫相关治疗。在SCLC中观察到的主要基因突变是TP53和RB1突变;然而,众所周知,这些分子尚未成为可靶向治疗的对象。近年来,研究揭示了其他常见的基因改变和激活的信号通路,这些可能是有效的治疗靶点。其中包括PTEN缺失、PI3K激活突变、NOTCH通路抑制和极光激酶激活。此外,FGFR1扩增、Hedgehog通路激活和修复蛋白PARP1似乎参与了SCLC的肿瘤发生。这些新发现确定了一些有趣的靶点。此外,免疫疗法试图在SCLC治疗中找到一席之地。免疫检查点抑制剂正在进行I期至III期临床试验。我们希望在未来几年,通过靶向治疗的应用和免疫疗法的引入,SCLC患者的治疗将得到改善。