De Mello Ramon Andrade Bezerra, Voscaboinik Rafael, Luciano João Vittor Pires, Cremonese Rafaela Vilela, Amaral Giovanna Araujo, Castelo-Branco Pedro, Antoniou Georgios
Division of Medical Oncology, Escola Paulista de Medicina, Hospital São Paulo, Universidade Federal de São Paulo (UNIFESP), Sao Paulo 04023-900, Brazil.
Faculdade de Medicina, Universidade Nove de Julho, Sao Paulo 04023-900, Brazil.
Cancers (Basel). 2021 Dec 28;14(1):122. doi: 10.3390/cancers14010122.
From a complete literature review, we were able to present in this paper what is most current in the treatment with immunotherapy for advanced non-small cell lung cancer (NSCLC). Especially the use of immunotherapy, particularly inhibitors of PD-1 (programmed cell death protein 1), PDL-1 (programmed cell death protein ligand 1), and CTLA-4 (cytotoxic T-lymphocyte antigen 4). Since 2015, these drugs have transformed the treatment of advanced NSCLC lacking driver mutations, evolving from second-line therapy to first-line, with excellent results. The arrival of new checkpoint inhibitors such as cemiplimab and the use of checkpoint inhibitors earlier in the therapy of advanced and metastatic cancers has been making the future prospects for treating NSCLC lacking driver mutations more favorable and optimistic. In addition, for those patients who have low PDL-1 positivity tumors, the combination of cytotoxic chemotherapy, VEGF inhibitor, and immunotherapy have shown an important improvement in global survival and progression free survival regardless the PDL-1 status. We also explored the effectiveness of adding radiotherapy to immunotherapy and the most current results about this combination. One concern that cannot be overlooked is the safety profile of immune checkpoint inhibitors (ICI) and the most common toxicities are described throughout this paper as well as tumor resistance to ICI.
通过全面的文献综述,我们能够在本文中呈现晚期非小细胞肺癌(NSCLC)免疫治疗的最新进展。特别是免疫疗法的应用,尤其是程序性死亡蛋白1(PD-1)抑制剂、程序性死亡蛋白配体1(PDL-1)抑制剂和细胞毒性T淋巴细胞相关抗原4(CTLA-4)抑制剂。自2015年以来,这些药物改变了缺乏驱动基因突变的晚期NSCLC的治疗模式,从二线治疗发展为一线治疗,疗效显著。新的检查点抑制剂如西米普利单抗的出现,以及在晚期和转移性癌症治疗中更早使用检查点抑制剂,使得缺乏驱动基因突变的NSCLC的未来治疗前景更加乐观。此外,对于那些肿瘤PDL-1低表达的患者,细胞毒性化疗、血管内皮生长因子(VEGF)抑制剂和免疫疗法的联合应用在总生存期和无进展生存期方面均有显著改善,且不受PDL-1状态影响。我们还探讨了免疫治疗联合放疗的有效性以及该联合治疗的最新结果。一个不容忽视的问题是免疫检查点抑制剂(ICI)的安全性,本文描述了最常见的毒性反应以及肿瘤对ICI的耐药性。