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