Coordination of anti-CTLA-4 with whole-brain radiation therapy decreases tumor burden during treatment in a novel syngeneic model of lung cancer brain metastasis

被引:2
作者
Blethen, K. E. [1 ]
Wolford, C. P. [1 ]
Pecar, G. L. [1 ]
Arsiwala, T. A. [1 ,2 ]
Adjeroh, E. [1 ]
Dykstra, L. P. [1 ]
Kielkowski, B. N. [1 ]
Lockman, P. R. [1 ]
机构
[1] West Virginia Univ, Sch Pharm, Dept Pharmaceut Sci, 108 Biomed Dr, Morgantown, WV 26506 USA
[2] West Virginia Univ, Rockefeller Neurosci Inst, 1 Med Ctr Dr, Morgantown, WV USA
基金
美国国家卫生研究院;
关键词
Immunotherapy; Immune checkpoint blockade; Brain metastasis; EGFR; Radiotherapy; NIVOLUMAB; OUTCOMES; EXPRESSION; DOCETAXEL; IMMUNE; CELLS;
D O I
10.1007/s00262-023-03599-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is the most common primary tumor to metastasize to the brain. Although advances in lung cancer therapy have increased rates of survival over the past few decades, control and treatment of lung cancer brain metastasis remains an urgent clinical need. Herein, we examine the temporal coordination of alpha-CTLA-4 administration in combination with whole-brain radiation therapy in a syngeneic preclinical model of lung cancer brain metastasis in both C57Bl/6 and athymic nude mice. Brain tumor burden, survival, and weight loss were monitored. Immunotherapy administration 24 h prior to irradiation resulted in increased brain tumor burden, while administration of immunotherapy 12 h after radiation decreased tumor burden. Neither of the treatments affected survival outcomes or weight loss due to brain tumor recurrence. These findings suggest that the coordination of alpha-CTLA-4 administration in addition to whole-brain radiation therapy may be a viable strategy for reduction of tumor burden for the management of lung cancer brain metastasis.
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收藏
页数:10
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