He Bo, Ganss Ruth
Cancer Microenvironment Laboratory, Harry Perkins Institute of Medical Research and the University of Western Australia Centre for Medical Research, The University of Western Australia, Nedlands, WA 6009, Australia.
Cancers (Basel). 2021 Feb 15;13(4):810. doi: 10.3390/cancers13040810.
Advanced metastatic cancer is rarely curable. While immunotherapy has changed the oncological landscape profoundly, cure in metastatic disease remains the exception. Tumor blood vessels are crucial regulators of tumor perfusion, immune cell influx and metastatic dissemination. Indeed, vascular hyperpermeability is a key feature of primary tumors, the pre-metastatic niche in host tissue and overt metastases at secondary sites. Combining anti-angiogenesis and immune therapies may therefore unlock synergistic effects by inducing a stabilized vascular network permissive for effector T cell trafficking and function. However, anti-angiogenesis therapies, as currently applied, are hampered by intrinsic or adaptive resistance mechanisms at primary and distant tumor sites. In particular, heterogeneous vascular and immune environments which can arise in metastatic lesions of the same individual pose significant challenges for currently approved drugs. Thus, more consideration needs to be given to tailoring new combinations of vascular and immunotherapies, including dosage and timing regimens to specific disease microenvironments.
晚期转移性癌症很少能治愈。虽然免疫疗法已深刻改变了肿瘤学格局,但转移性疾病的治愈仍是个例外。肿瘤血管是肿瘤灌注、免疫细胞流入和转移扩散的关键调节因子。事实上,血管高通透性是原发性肿瘤、宿主组织中的前转移生态位以及继发性部位明显转移灶的一个关键特征。因此,联合抗血管生成和免疫疗法可能通过诱导一个稳定的血管网络,有利于效应T细胞的运输和功能,从而产生协同效应。然而,目前应用的抗血管生成疗法受到原发性和远处肿瘤部位的内在或适应性耐药机制的阻碍。特别是,同一个体转移病灶中可能出现的异质性血管和免疫环境,给目前已获批的药物带来了重大挑战。因此,需要更多地考虑针对特定疾病微环境量身定制血管和免疫疗法的新组合,包括剂量和给药方案。