PD-1/PD-L1 blockade therapy with atezolizumab: a new paradigm in the treatment of non-small cell lung cancer (NSCLC).

IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Samaneh Moradi, Pedram Sarikhani, Rafid Jihad Albadr, Waam Mohammed Taher, Mariem Alwan, Mahmood Jasem Jawad, Hiba Mushtaq, Niyousha Vakilzadehian
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Abstract

Now, platinum-based chemotherapy is used as the first-line treatment for advanced non-small cell lung cancer (NSCLC). Interestingly, a combination of immune checkpoint inhibitors, such as mepolizumab, with other targeted therapies and chemotherapy help to make a significant improvement. Atezolizumab, a fully humanized, engineered monoclonal antibody of IgG1 isotype against the protein programmed cell death-ligand 1 (PD-L1), blocks PD-1 activation and results in T-cell activity against tumor cells. As the second-line treatment of advanced or metastatic NSCLC, atezolizumab plus chemotherapy was approved in 2017 concerning the clinical benefit of the phase III OAK trials. Atezolizumab, compared with docetaxel, remarkably increased overall survival (OS) and showed promising efficacy and tolerability in the treatment of advanced NSCLC.Research on atezolizumab's application in neoadjuvant (pre-surgery) and adjuvant (post-surgery) contexts is ongoing. It is now undergoing trials to assess its efficacy in these settings, which may broaden its place in the NSCLC therapy spectrum and enhance long-term results. This paper briefly summarizes the clinical data of atezolizumab therapy alone or in combination with other therapeutics for NSCLC therapy.

atezolizumab PD-1/PD-L1阻断治疗:非小细胞肺癌(NSCLC)治疗的新范式
目前,铂类化疗已成为晚期非小细胞肺癌(NSCLC)的一线治疗方案。有趣的是,免疫检查点抑制剂(如mepolizumab)与其他靶向治疗和化疗的组合有助于显著改善。Atezolizumab是一种完全人源化、工程化的IgG1同型单克隆抗体,针对蛋白程序性细胞死亡配体1 (PD-L1),阻断PD-1的激活,并导致t细胞对肿瘤细胞的活性。作为晚期或转移性NSCLC的二线治疗,atezolizumab联合化疗于2017年获得批准,涉及III期OAK试验的临床效益。与多西他赛相比,Atezolizumab显著提高了总生存期(OS),并在治疗晚期NSCLC中显示出良好的疗效和耐受性。atezolizumab在新辅助(术前)和辅助(术后)环境中的应用研究正在进行中。目前正在进行试验以评估其在这些情况下的疗效,这可能会扩大其在非小细胞肺癌治疗谱中的地位并提高长期疗效。本文简要总结了atezolizumab单独或联合其他药物治疗非小细胞肺癌的临床资料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Discover. Oncology
Discover. Oncology Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.40
自引率
9.10%
发文量
122
审稿时长
5 weeks
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