Novel Combination Treatment for Melanoma: FLASH Radiotherapy and Immunotherapy Delivered by a Radiopaque and Radiation Responsive Hydrogel

黑色素瘤 免疫疗法 放射治疗 医学 闪光灯(摄影) 癌症研究 联合疗法 体内 免疫系统 免疫学 内科学 生物 艺术 生物技术 视觉艺术
作者
Yuxi C. Dong,Lenitza M. Nieves,Jessica C. Hsu,Ananyaa Kumar,Mathilde Bouché,Uma Maheswari Krishnan,Katherine J. Mossburg,Deeksha Saxena,Selen Uman,Taku Kambayashi,Jason A. Burdick,Michele M. Kim,Jay F. Dorsey,David P. Cormode
出处
期刊:Chemistry of Materials [American Chemical Society]
卷期号:35 (22): 9542-9551 被引量:12
标识
DOI:10.1021/acs.chemmater.3c01390
摘要

Immunotherapies have become the standard treatment for melanoma. To further improve patient responses, combinations of immunotherapies and radiotherapy (RT) are being studied, since radiotherapies can potentially provide additional immune stimulation, in addition to direct antitumor effects. FLASH-RT is a novel, ultrahigh dose rate, radiation delivery approach, with the potential of at least equivalent tumor control efficacy and reduced damage to healthy tissue. However, the effects of combining FLASH-RT and immunotherapy have not been extensively studied in melanoma. Toll-like receptor (TLR) agonists, such as imiquimod (IMQ), are potent immunostimulatory agents, although their utility is limited due to poor solubility and systemic side effects. We therefore developed a novel combination therapy for melanoma consisting of IMQ delivered to the tumor via a radiopaque and radiation responsive hydrogel combined with FLASH-RT. We found that FLASH was able to effectively stimulate IMQ release from the hydrogel. In addition, we found that the combination of FLASH and released IMQ resulted in synergistic melanoma cell killing in vitro. The combination therapy reduced tumor growth compared to controls, enhanced survival, and resulted in remarkable enhancements in certain tumor cytokine levels. CT imaging allowed the hydrogel to be monitored in vivo. In addition, no adverse effects of the treatment were observed. Overall, this IMQ-gel and FLASH-RT combination may have potential as an improved treatment for melanoma and indicates that the interactions of FLASH-RT and TLR agonists merit further study.
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