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新型 MRI 引导聚焦超声刺激微泡辐射增强治疗乳腺癌。

Novel MRI-guided focussed ultrasound stimulated microbubble radiation enhancement treatment for breast cancer.

机构信息

Department of Radiation Oncology, Sunnybrook Health Sciences Centre, 2075 Bayview Avenue, T2, Toronto, ON, M4N3M5, Canada.

Department of Radiation Oncology, University of Toronto, Toronto, Canada.

出版信息

Sci Rep. 2023 Aug 21;13(1):13566. doi: 10.1038/s41598-023-40551-5.

Abstract

Preclinical studies have demonstrated focused ultrasound (FUS) stimulated microbubble (MB) rupture leads to the activation of acid sphingomyelinase-ceramide pathway in the endothelial cells. When radiotherapy (RT) is delivered concurrently with FUS-MB, apoptotic pathway leads to increased cell death resulting in potent radiosensitization. Here we report the first human trial of using magnetic resonance imaging (MRI) guided FUS-MB treatment in the treatment of breast malignancies. In the phase 1 prospective interventional study, patients with breast cancer were treated with fractionated RT (5 or 10 fractions) to the disease involving breast or chest wall. FUS-MB treatment was delivered before 1st and 5th fractions of RT (within 1 h). Eight patients with 9 tumours were treated. All 7 evaluable patients with at least 3 months follow-up treated for 8 tumours had a complete response in the treated site. The maximum acute toxicity observed was grade 2 dermatitis in 1 site, and grade 1 in 8 treated sites, at one month post RT, which recovered at 3 months. No RT-related late effect or FUS-MB related toxicity was noted. This study demonstrated safety of combined FUS-MB and RT treatment. Promising response rates suggest potential strong radiosensitization effects of the investigational modality.Trial registration: clinicaltrials.gov, identifier NCT04431674.

摘要

临床前研究表明,聚焦超声(FUS)刺激微泡(MB)破裂会导致内皮细胞中酸性鞘磷脂酶-神经酰胺途径的激活。当放射治疗(RT)与 FUS-MB 同时进行时,凋亡途径导致细胞死亡增加,从而产生强烈的放射增敏作用。在这里,我们报告了首例使用磁共振成像(MRI)引导 FUS-MB 治疗治疗乳腺癌的人体试验。在这项 1 期前瞻性介入研究中,患有乳腺癌的患者接受了分次 RT(5 或 10 次)治疗,包括乳房或胸壁受累的疾病。FUS-MB 治疗在 RT 的第 1 次和第 5 次(在 1 小时内)之前给予。共有 8 名患者和 9 个肿瘤接受了治疗。所有 7 名可评估的患者(至少随访 3 个月)接受了 8 个肿瘤的治疗,在治疗部位均有完全缓解。在 RT 后 1 个月观察到的最大急性毒性为 1 个部位的 2 级皮炎,8 个治疗部位的 1 级,在 3 个月时恢复。未观察到与 RT 相关的迟发性效应或 FUS-MB 相关毒性。这项研究证明了联合 FUS-MB 和 RT 治疗的安全性。有希望的反应率表明该研究方法具有潜在的强烈放射增敏作用。试验注册:clinicaltrials.gov,标识符 NCT04431674。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/900f/10442356/705d4ddf6404/41598_2023_40551_Fig1_HTML.jpg

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