Benson Zachary, Manjili Saeed H, Habibi Mehran, Guruli Georgi, Toor Amir A, Payne Kyle K, Manjili Masoud H
Department of Internal Medicine, Virginia Commonwealth University School of Medicine, USA.
Department of Biomedical Engineering, Virginia Commonwealth University School of Engineering, USA.
Biochem Pharmacol. 2017 Dec 1;145:12-17. doi: 10.1016/j.bcp.2017.08.007. Epub 2017 Aug 10.
Recent advances in the treatment of melanoma and non-small cell lung cancer (NSCLC) by combining conventional therapies with anti-PD1/PD-L1 immunotherapies, have renewed interests in immunotherapy of cancer. The emerging concept of conventional cancer therapies combined with immunotherapy differs from the classical concept in that it is not simply taking advantage of their additive anti-tumor effects, but it is to use certain therapeutic regimens to condition the tumor microenvironment for optimal response to immunotherapy. To this end, low dose immunogenic chemotherapies, epigenetic modulators and inhibitors of cell cycle progression are potential candidates for rendering tumors highly responsive to immunotherapy. Next generation immunotherapeutics are therefore predicted to be highly effective against cancer, when they are used following appropriate immune modulatory compounds or targeted delivery of tumor cell cycle inhibitors using nanotechnology.
通过将传统疗法与抗PD1/PD-L1免疫疗法相结合来治疗黑色素瘤和非小细胞肺癌(NSCLC)的最新进展,重新激发了人们对癌症免疫疗法的兴趣。传统癌症疗法与免疫疗法相结合的新兴概念与经典概念不同,在于它不仅仅是利用它们相加的抗肿瘤作用,而是使用某些治疗方案来调节肿瘤微环境以实现对免疫疗法的最佳反应。为此,低剂量免疫原性化疗、表观遗传调节剂和细胞周期进展抑制剂是使肿瘤对免疫疗法高度敏感的潜在候选药物。因此,预计下一代免疫疗法在与适当的免疫调节化合物联合使用或使用纳米技术靶向递送肿瘤细胞周期抑制剂后,对癌症将具有高度疗效。