In Vitro Investigation of Renal Cell Carcinoma Response to Combination Sorafenib and Cryoablation Treatment

John M. Baust, Kimberly L. Santucci, Kristi K. Snyder, A. Robilotto, John G. Baust, R. V. Van Buskirk, Thomas J. Polascik
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Abstract

The 5-year survival rate for localized kidney cancer is 93%, but only 13% for those presenting with metastatic disease (2019 SEER data). Cryosurgery is an established treatment modality for renal cell cancer (RCC), with outcomes showing equipoise to radiofrequency ablation (RFA) and partial nephrectomy. Sorafenib is a targeted therapy for RCC utilized in more advanced stage diseases. Given the success of both cryoablation and sorafenib as monotherapies for RCC, in this study, we investigated the cellular response of RCC to combinatorial sorafenib pre-treatment and cryoablation in vitro using cell culture and tissue-engineered tumor models. In vitro samples were exposed to a single or repeat (double) 5-minute freeze at -10°C, -15°C, or -20°C representing temperatures within the periphery of a cryolesion. A repeat freeze to -20°C was necessary to fully ablate samples yielding day 1 viability of 2.9% (±0.2) with no recovery observed over the 7 days post-treatment culture. These findings were consistent with published data on the lethal temperature in RCC, suggesting that -25°C is necessary to destroy RCC following a single freeze event. Pre-treatment of samples with sorafenib at concentrations of 10.61 and 21.21 µM (½ clinical and clinical dose, respectively) was combined with a single or repeat 5-minute freeze to -10°C, -15°C, or -20°C. At the time of drug removal (day 0/pre-freeze), 10.61 µM sorafenib treated samples yielded 25.3% (±0.4) viability, yet samples regrew to control levels by day 7. Following combination freeze and sorafenib exposure, sample viability was found to be 27.5% (±0.7), 2.9% (±0.4), and 0.2% (±0.02) following a single freeze and 15.6% (±0.5), 0.7% (±0.1), and 0.1% (±0.01) following a repeat (double freeze), respectively. Regrowth was observed over the 7-day assessment period in samples exposed to a -10°C single or double freeze and a -15°C single freeze, but not in the -20°C single freeze or -15°C double freeze conditions. Thus, pre-treatment with 10.61 µM sorafenib was found to increase the minimum lethal temperature from the reported -25°C to -20°C following a single freeze event and from -20°C to -15°C following a double freeze. Results of the cell culture studies were confirmed in the 3D tissue-engineered tumor model, wherein the combination of 10.61 µM sorafenib and freezing was found to further increase the lethal temperature from <-20°C to -15°C following a single freeze event. This increased freeze susceptibility yielded a 32% improvement in the overall ablative volume of the ice ball following combinatorial treatment versus freezing alone. These in vitro results suggest that the combination of sorafenib and cryoablation may provide a possible combinatorial treatment path for RCC.
索拉非尼联合冷冻消融治疗肾细胞癌疗效的体外研究
局部肾癌的5年生存率为93%,但转移性肾癌的5年生存率仅为13%(2019年SEER数据)。冷冻手术是肾细胞癌(RCC)的一种既定治疗方式,其结果与射频消融(RFA)和部分肾切除术相当。索拉非尼是一种用于晚期疾病的RCC靶向治疗药物。鉴于冷冻消融和索拉非尼作为RCC单药治疗的成功,在本研究中,我们利用细胞培养和组织工程肿瘤模型研究了RCC对体外联合索拉非尼预处理和冷冻消融的细胞反应。体外样品暴露于-10°C, -15°C或-20°C的单次或重复(两次)冷冻5分钟,代表冷冻创口周围的温度。需要重复冷冻至-20°C才能完全消融样品,产生2.9%(±0.2)的第1天存活率,并且在处理后培养的7天内未观察到恢复。这些发现与已发表的关于碾压混凝土致死温度的数据一致,表明-25°C是在单次冻结事件后破坏碾压混凝土所必需的。用浓度为10.61和21.21µM(分别为½临床和临床剂量)的索拉非尼对样品进行预处理,并将样品单次或重复冷冻至-10°C、-15°C或-20°C,冷冻5分钟。在去除药物(第0天/预冷冻)时,10.61µM索拉非尼处理的样品产生25.3%(±0.4)的活力,但样品在第7天恢复到控制水平。联合冷冻和索拉非尼暴露后,单次冷冻后样品活力分别为27.5%(±0.7)、2.9%(±0.4)和0.2%(±0.02),重复(两次冷冻)后分别为15.6%(±0.5)、0.7%(±0.1)和0.1%(±0.01)。在7天的评估期内,暴露于-10°C单次或双次冻结和-15°C单次冻结的样品观察到再生,但在-20°C单次冻结或-15°C双次冻结条件下没有观察到再生。因此,10.61µM索拉非尼预处理被发现可以将最低致死温度从报道的单次冷冻事件后的-25°C提高到-20°C,将双次冷冻后的-20°C提高到-15°C。在3D组织工程肿瘤模型中证实了细胞培养研究的结果,其中10.61µM索拉非尼和冷冻的组合被发现在单次冷冻事件后进一步将致死温度从<-20°C提高到-15°C。与单独冷冻相比,联合治疗后,冷冻敏感性的增加使冰球的总消融体积提高了32%。这些体外实验结果表明,索拉非尼联合冷冻消融可能为RCC提供一种可能的联合治疗途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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