原发性乳腺癌整体冷冻辅助切除及肿瘤冷冻消融与局部给药及肿瘤液靶向相关。实验及临床研究

M. M. Korpan, Yueyong Xiao, Xiao-Ou He, O. Dronov
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引用次数: 0

摘要

目的:采用冷冻手术联合肿瘤周围和肿瘤内同时注射示踪剂蓝色染料进行进一步的淋巴定位治疗原发性乳腺肿瘤。评价术中低温探针辅助注射蓝色染料和细胞毒性示踪剂混合物用于VX2肿瘤模型局部靶向药物的有效性,以及其在单独使用蓝色染料的低温辅助乳腺肿瘤手术中的翻译意义。前哨淋巴结作图,病理确定肿瘤,切除边缘是可以实现的。材料和方法。随机选择39例I至IV期原发性乳腺癌患者,年龄52,4(±19)岁(平均,标准差(SD)年),在奥地利维也纳Rudolfinerhaus私人诊所接受治疗,并纳入本初步临床研究。在计算机断层扫描引导下,我们将5份2ml的细胞毒性示踪剂混合物注射到16个冷冻或常温VX2肿瘤的边缘。我们通过计算机断层扫描、大体检查和组织病理学评估术中和术后肿瘤-宿主界面的药物靶向和治疗效果。在34例T1至T4期原发性乳腺癌患者中,我们进行了超声引导下的冷冻探针辅助肿瘤冻融循环、蓝色染料引导下的淋巴定位和手术。我们检查了术中和刚切除的标本,以及肿瘤-宿主界面、淋巴结、乳腺实质和切除腔中的蓝色染料分布模式。结果:38例患者中有29例为局部原发性乳腺癌,估计无需新辅助化疗即可切除。87%的患者有1 ~ 12个腋窝淋巴结染色,72%的患者有另一象限和切除腔染色。无论冷冻剂量、冻融周期次数、药物剂量分割、肿瘤特征或肿瘤尺寸如何,液体不透水的冷冻VX2或乳腺肿瘤在肿瘤-宿主界面以弧形模式运输药物。在熔化过程中,细胞毒性示踪剂混合物在VX2肿瘤的50%范围内扩散,并反映了肿瘤-宿主界面的扩散;这在正常情况下是巨大的。在VX2中,CT间隙在病理上对应灶缘坏死的20%。在这两项研究中,蓝色染料剂量染色在肿瘤-宿主界面和肿瘤中呈线性扩散。结论。该研究为原发性乳腺癌的术中冷冻辅助治疗方案铺平了道路。我们已经证明,我们的冷冻技术可以反复冷冻深层肿瘤,用于整体切除或原发乳腺癌的原位消融,在白条监测的帮助下,可以在常规手术期间同时注射染料示踪剂,这样就可以进行淋巴定位。在乳腺癌冷冻辅助手术中,术中冷冻辅助给药和靶向技术在VX2肿瘤冷冻消融过程中成功地转化为局部蓝色染料靶向和淋巴定位。我们探索了我们的策略,以防止肿瘤细胞迁移的能力,而不是注射示踪剂,在常规切除冷冻乳腺恶性肿瘤的淋巴血管引流。
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Cryo-assisted resection of primary breast cancer en bloc and tumor cryoablation connected with local drug delivery and targeting of tumor fluids. Experimental and clinical studies
Objective — to use cryosurgery in combination with simultaneous peritumoral and intratumoral tracer injections of blue dye for further lymphatic mapping in the treatment of primary breast tumors. The effectiveness of intraoperative cryoprobe‑assisted injection of blue dye and cytotoxic‑tracer mixture for locoregional drug targeting in the VX2 tumor model as well as its translational significance for cryo‑assisted breast tumor surgery with blue dye alone were evaluated. Sentinel lymph node mapping, pathological determination of the tumor, and resection margins were achievable. Materials and methods. Thirty‑nine patients with primary breast cancer in stages I to IV, aged 52,4 (±19) years (mean, standard deviation (SD) years), were randomly selected, treated at the Rudolfinerhaus Private Clinic in Vienna, Austria, and included in this preliminary clinical study. Under computed tomography guidance, we injected 2 ml of cytotoxic‑tracer mixture in five aliquots into the margins of 16 frozen or normothermic VX2 tumors.  We evaluated the intraoperative and post‑operative drug targeting and therapeutic efficacy at the tumor‑host interface by means of computer tomography, gross examination, and histopathology. In thirty‑four T1 to T4 primary breast cancers, we performed an ultrasound‑guided cryoprobe‑assisted tumor freezing‑thawing cycle, blue dye‑guided lymphatic mapping, and surgery. We examined an intraoperative and freshly resected specimen and the blue dye distribution pattern in the tumor‑host interface, lymph node(s), breast parenchyma, and resection cavity.   Results. 29 of the 38 patients had localized primary breast cancer, which was estimated to be resectable without neoadjuvant chemotherapy. 87% of patients had one to twelve stained axillary lymph nodes, while 72% of patients had another quadrant and resection cavity stained.  Fluid‑impervious frozen VX2 or breast tumors transported drug(s) in an arc‑like pattern at the tumor‑host interface regardless of freeze dose, number of freeze‑thaw cycles, drug dose fractionation, tumor characteristics, or tumor dimensions. During melting, the cytotoxic‑tracer mixture spread within 50% of the VX2 tumor and mirrored that of the tumor‑host interface; it was massive in normothermia. In VX2, the CT gap corresponded to 20% of the focal margin necrosis in pathology. In both studies, blue dye dose‑staining spread linearly in the tumor‑host interface and tumor. Conclusions. The study paves the way for intraoperative cryo‑assisted cure options for primary breast cancer. We have shown that our cryosurgical technique of repeatedly freezing deep tumors for en bloc resection or for in situ ablation of primary breast cancer, facilitated by IOUS monitoring, can be coupled with the simultaneous injection of dye tracers during conventional surgery, which then allows for lymphatic mapping. Intraoperative freezing‑assisted drug delivery and targeting techniques during cryoablation of the VX2 tumor translate successfully to locoregional blue dye targeting and lymphatic mapping during cryo‑assisted surgery of breast cancer. We explored the ability of our strategy to prevent tumor cell migration, but not that of injected tracers, to the lymphovascular drainage during conventional resection of frozen breast malignancies.  
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