Kim Minhyung, Neznanov Nickolay, Wilfong Chandler D, Fleyshman Daria I, Purmal Andrei A, Haderski Gary, Stanhope-Baker Patricia, Burkhart Catherine A, Gurova Katerina V, Gudkov Andrei V, Skitzki Joseph J
Department of Surgical Oncology, Roswell Park Cancer Institute, Buffalo, New York.
Department of Immunology, Roswell Park Cancer Institute, Buffalo, New York.
Cancer Res. 2016 Nov 15;76(22):6620-6630. doi: 10.1158/0008-5472.CAN-15-2764. Epub 2016 Sep 28.
Isolated limb perfusion (ILP) with the chemotherapeutic agent melphalan is an effective treatment option for extremity in-transit melanoma but is toxic and technically challenging to deliver locoregionally. CBL0137 is an experimental clinical drug with broad anticancer activity in animal models, owing to its ability to bind DNA in a nongenotoxic manner and inactivate the FACT chromatin modulator essential for tumor cell viability. Here, we report that CBL0137 delivered by ILP in a murine melanoma model is as efficacious as melphalan, displaying antitumor activity at doses corresponding to only a fraction of the systemic MTD of CBL0137. The ability to bind DNA quickly combined with a favorable safety profile made it possible to substitute CBL0137 in the ILP protocol, using an intra-arterial infusion method, to safely achieve effective tumor suppression. Our findings of a preclinical proof of concept for CBL0137 and its administration via intra-arterial infusion as a superior treatment compared with melphalan ILP allows for locoregional treatment anywhere a catheter can be placed. Cancer Res; 76(22); 6620-30. ©2016 AACR.
使用化疗药物美法仑进行孤立肢体灌注(ILP)是治疗肢体移行性黑色素瘤的一种有效治疗选择,但具有毒性,且在局部给药时技术上具有挑战性。CBL0137是一种实验性临床药物,在动物模型中具有广泛的抗癌活性,因为它能够以非基因毒性方式结合DNA并使肿瘤细胞存活所必需的FACT染色质调节剂失活。在此,我们报告,在小鼠黑色素瘤模型中通过ILP给药的CBL0137与美法仑一样有效,在仅相当于CBL0137全身最大耐受剂量一小部分的剂量下显示出抗肿瘤活性。快速结合DNA的能力与良好的安全性相结合,使得使用动脉内输注方法在ILP方案中替代CBL0137成为可能,从而安全地实现有效的肿瘤抑制。我们关于CBL0137及其通过动脉内输注给药作为比美法仑ILP更优治疗方法的临床前概念验证的研究结果,使得在任何能够放置导管的地方都可以进行局部治疗。《癌症研究》;76(22);6620 - 30。©2016美国癌症研究协会。