一种提高放射治疗效果的新策略:首次在人类MR引导下聚焦超声刺激微泡(MRgFUS+MB)放射增强治疗中

Moore-Palhares Daniel, Saifuddin Murtuza, Ho Ling, Lu Lin, Dasgupta Archya, Smoragiewicz Martin, Karam Irene, Bayley Andrew, Sahgal Arjun, Poon Ian, Czarnota Gregory J
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引用次数: 0

摘要

背景和目的:临床前的体外和体内实验表明,与聚焦超声(FUS)刺激的微泡(MB)相结合,辐射诱导的肿瘤细胞死亡可以增加10至40倍。MB在肿瘤体积中的声学暴露导致血管系统扰动、酸性鞘磷脂酶(ASMase)神经酰胺通路的激活,并导致内皮细胞凋亡。当肿瘤随后接受放射治疗时,内皮细胞死亡和缺氧性肿瘤杀伤增加。在这里,我们描述了人类首次使用磁共振(MR)引导的FUS刺激MB(MRgFUS+MB)辐射增强治疗患者的经验。病例介绍:一名患有复发性疾病的癌症头颈部患者接受了局部疾病5个不同部位的放射治疗,然后进行了全身治疗。第一个疗程为45 Gy,单独分为5个部分,第二个疗程为30 Gy,5个部分伴热疗,另外三个疗程为20-30 Gy,伴MRgFUS+MB治疗。该治疗方法使用在500KHz和540kPa峰值负压下操作的MR耦合FUS装置,在5分钟内具有750ms的穿透时间,以刺激肿瘤靶内静脉内给予的MB。所有用刺激MB治疗的部位都有完全的放射学反应,随后,患者的其他皮肤转移性疾病消失了。该患者已经接受了两年多的监测,没有积极治疗或疾病进展。讨论:MRgFUS+MB耐受性良好,无治疗相关不良事件报告,这可归因于FUS能够选择性刺激肿瘤体积内的MB,同时保留周围的正常组织。所有靶位点的持续局部控制与早期临床前发现一致,表明FUS+MB具有辐射增强潜力。结论:MRgFUS+MB是一种新的、有前景的治疗方法,可以提高放疗疗效,改善治疗指标,并有可能改善疾病控制。
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A Novel Strategy to Improve Radiotherapy Effectiveness: First-in-Human MR-guided Focused Ultrasound-Stimulated Microbubbles (MRgFUS+MB) Radiation Enhancement Treatment
Background and aim: Preclinical in vitro and in vivo experiments suggest that radiation-induced tumour cell death can be enhanced 10- to 40-fold when combined with focused-ultrasound (FUS)-stimulated microbubbles (MB). The acoustic exposure of MB in the tumour volume causes vasculature perturbation, activation of the acid sphingomyelinase (ASMase) ceramide pathway, and resultant endothelial cell apoptosis. When the tumour is subsequently treated with radiation, there is increased endothelial cell death and anoxic tumour killing. Here we describe a first-in-human experience treating patients with magnetic resonance (MR)-guided FUS-stimulated MB (MRgFUS+MB) radiation enhancement. Case presentation: A head and neck cancer patient with recurrent disease underwent radiotherapy for 5 separate sites of locoregional disease followed by systemic therapy. The first consisted of a course of 45 Gy in 5 fractions alone, the second of 30 Gy in 5 fractions with hyperthermia, and the three others of 20-30 Gy in 5 fractions along with MRgFUS+MB treatment. The treatment methodology used an MR-coupled FUS-device operating at 500 KHz and 540 kPa peak negative pressure with an insonification time of 750 ms spread over 5 minutes to stimulate intravenously administered MB within tumour target. All sites treated with stimulated MB had a complete radiological response, and subsequently, the patient’s other cutaneous metastatic disease disappeared. The patient has been under surveillance for over two years without active treatment or disease progression. Discussion: MRgFUS+MB was well-tolerated with no reported treatment-related adverse events, which can be attributed to the capability of FUS to selectively stimulate MB within the tumour volume while sparing the surrounding normal tissue. Sustained local control at all target sites aligns with earlier preclinical findings suggesting the radiation enhancement potential of FUS+MB. Conclusion: MRgFUS+MB represents a novel and promising therapy for enhancing radiation efficacy and improving therapeutic index with potential improvements in disease control.
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