Abdallah Mahmoud, Voland Rick, Decamp Malcolm, Flickinger John, Pacioles Toni, Jamil Muhammad, Silbermins Damian, Shenouda Mina, Valsecchi Matias, Bir Arvinder, Shweihat Yousef, Bastidas Juan, Chowdhury Nepal, Kachynski Yury, Eldib Howide, Wright Thomas, Mahdi Ahmad, Al-Nusair Jowan, Nwanwene Kemnasom, Varlotto John
Department of Oncology, Edwards Comprehensive Cancer Institute, Marshall University, Huntington, WV 25701, USA.
Department of Ophthalmology, University of Wisconsin, Madison, WI 53705, USA.
Cancers (Basel). 2024 Dec 17;16(24):4207. doi: 10.3390/cancers16244207.
Immunotherapy has made recent improvements in disease-free survival (DFS) and/or overall survival (OS) in all stages of non-small-cell lung cancer (NSCLC). Here, we review the tumor microenvironment and its immunosuppressive effects and discuss how anti-angiogenic therapies may potentiate the anti-carcinogenic effects of immunotherapy. We also review all the past literature and discuss strategies of combining anti-angiogenic therapy and immunotherapy +/- chemotherapy and hypothesize how we can use this strategy for non-small-cell lung cancer in metastatic previously untreated/previously treated settings in previously treated EGFR-mutated NSCLC for the upfront treatment of brain metastases prior to radiation therapy and for the incorporation of this strategy into stage III unresectable disease. We assert the use of anti-angiogenic therapy and immunotherapy when combined appropriately with chemotherapy and radiotherapy has the potential to increase the long-term survivals in both the stage III and metastatic setting so that we can now consider more patients to experience curative treatment.
免疫疗法最近在非小细胞肺癌(NSCLC)各阶段的无病生存期(DFS)和/或总生存期(OS)方面取得了进展。在此,我们回顾肿瘤微环境及其免疫抑制作用,并讨论抗血管生成疗法如何增强免疫疗法的抗癌作用。我们还回顾了所有既往文献,讨论了联合抗血管生成疗法与免疫疗法+/-化疗的策略,并推测如何将该策略用于转移性非小细胞肺癌患者,包括既往未治疗/既往接受过治疗的患者、既往接受过治疗的EGFR突变型非小细胞肺癌患者、放疗前脑转移的一线治疗以及将该策略纳入III期不可切除疾病的治疗。我们认为,抗血管生成疗法和免疫疗法与化疗和放疗适当联合使用,有可能提高III期和转移性患者的长期生存率,从而使更多患者有望接受治愈性治疗。