Hay Alayna N, Aycock Kenneth N, Lorenzo Melvin F, David Kailee, Coutermarsh-Ott Sheryl, Salameh Zaid, Campelo Sabrina N, Arroyo Julio P, Ciepluch Brittany, Daniel Gregory, Davalos Rafael V, Tuohy Joanne
Department of Small Animal Clinical Sciences, Virginia Maryland College of Veterinary Medicine, Blacksburg, VA 24061, USA.
Virginia Tech Animal Cancer Care and Research Center, Virginia Maryland College of Veterinary Medicine, Roanoke, VA 24016, USA.
Biomedicines. 2024 Sep 7;12(9):2038. doi: 10.3390/biomedicines12092038.
In this study, the feasibility of treating canine primary lung tumors with high-frequency irreversible electroporation (H-FIRE) was investigated as a novel lung cancer treatment option. H-FIRE is a minimally invasive tissue ablation modality that delivers bipolar pulsed electric fields to targeted cells, generating nanopores in cell membranes and rendering targeted cells nonviable. In the current study, canine patients ( = 5) with primary lung tumors underwent H-FIRE treatment with an applied voltage of 2250 V using a 2-5-2 µs H-FIRE waveform to achieve partial tumor ablation prior to the surgical resection of the primary tumor. Surgically resected tumor samples were evaluated histologically for tumor ablation, and with immunohistochemical (IHC) staining to identify cell death (activated caspase-3) and macrophages (IBA-1, CD206, and iNOS). Changes in immunity and inflammatory gene signatures were also evaluated in tumor samples. H-FIRE ablation was evident by the microscopic observation of discrete foci of acute hemorrhage and necrosis, and in a subset of tumors ( = 2), we observed a greater intensity of cleaved caspase-3 staining in tumor cells within treated tumor regions compared to adjacent untreated tumor tissue. At the study evaluation timepoint of 2 h post H-FIRE, we observed differential gene expression changes in the genes , , , , and in treated tumor regions relative to paired untreated tumor regions. Additionally, we preliminarily evaluated the technical feasibility of delivering H-FIRE percutaneously under CT guidance to canine lung tumor patients ( = 2). Overall, H-FIRE treatment was well tolerated with no adverse clinical events, and our results suggest H-FIRE potentially altered the tumor immune microenvironment.
在本研究中,研究了使用高频不可逆电穿孔(H-FIRE)治疗犬原发性肺肿瘤作为一种新型肺癌治疗选择的可行性。H-FIRE是一种微创组织消融方式,可将双相脉冲电场传递至靶细胞,在细胞膜上产生纳米孔并使靶细胞失去活性。在当前研究中,5只患有原发性肺肿瘤的犬患者在手术切除原发性肿瘤之前,使用2-5-2微秒的H-FIRE波形,以2250V的施加电压接受H-FIRE治疗,以实现部分肿瘤消融。对手术切除的肿瘤样本进行组织学评估以确定肿瘤消融情况,并通过免疫组织化学(IHC)染色来识别细胞死亡(活化的半胱天冬酶-3)和巨噬细胞(IBA-1、CD206和诱导型一氧化氮合酶)。还评估了肿瘤样本中免疫和炎症基因特征的变化。通过显微镜观察急性出血和坏死的离散病灶可明显看出H-FIRE消融,并且在一部分肿瘤(n = 2)中,我们观察到与相邻未治疗的肿瘤组织相比,治疗肿瘤区域内肿瘤细胞中裂解的半胱天冬酶-3染色强度更高。在H-FIRE后2小时的研究评估时间点,我们观察到与配对的未治疗肿瘤区域相比,治疗肿瘤区域中基因、、、和的基因表达发生了差异变化。此外,我们初步评估了在CT引导下经皮向犬肺肿瘤患者(n = 2)提供H-FIRE的技术可行性。总体而言,H-FIRE治疗耐受性良好,没有不良临床事件,我们的结果表明H-FIRE可能改变了肿瘤免疫微环境。