Recent advances in immune checkpoint therapy in non-small cell lung cancer and opportunities for nanoparticle-based therapy

易普利姆玛 无容量 阿替唑单抗 彭布罗利珠单抗 免疫检查点 医学 阿维鲁单抗 银耳霉素 肺癌 免疫疗法 肿瘤科 免疫系统 癌症研究 免疫学 杜瓦卢马布
作者
Mohammad‐Javad Sanaei,Atieh Pourbagheri‐Sigaroodi,Vahid Kaveh,Hassan Abolghasemi,Seyed H. Ghaffari,Majid Momeny,Davood Bashash
出处
期刊:European Journal of Pharmacology [Elsevier BV]
卷期号:909: 174404-174404 被引量:24
标识
DOI:10.1016/j.ejphar.2021.174404
摘要

Non-small cell lung cancer (NSCLC) is the most common type of lung cancer with the highest mortality rate and a poor 5-year survival rate. The majority of the cases are diagnosed in advanced stages when the disease has spread, which makes the tumor inoperable. Due to the antigenic essence of lung tumor cells, immunotherapy is a novel area and has exhibited remarkable results in this malignancy. Immune checkpoint inhibitors are inhibitory molecules that disrupt immune checkpoint signaling pathways whether in the immune cells or tumor cells. Tremelimumab and ipilimumab (CTLA-4 blockers), pembrolizumab and nivolumab (PD-1 blockers), and durvalumab, avelumab, and atezolizumab (PD-L1 blockers) are FDA-approved and improve the survival and objective response of NSCLC patients. Despite this, over-stimulation of the immune system via the immune checkpoint therapy is a double-edged sword that causes a spectrum of adverse events from moderate to life-threatening. Nanomedicine considerably impacts the way of diagnosis and treatment of tumors to overcome treatment-related challenges. Accordingly, nanoparticle-based immune checkpoint inhibitor therapy increases the local concentration of immune checkpoint inhibitors while reduces the side effects, which result in boosting the anti-tumor immunity against various types of malignancies, including NSCLC. The current review provides comprehensive information about immune checkpoint therapy in NSCLC, their efficacy, and their safety profile. Besides, recent advances in nanoparticle-based immune checkpoint therapy and its limitation are discussed.

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