Millul Jacopo, Krudewig Christiane, Zana Aureliano, Dakhel Plaza Sheila, Puca Emanuele, Villa Alessandra, Neri Dario, Cazzamalli Samuele
Philochem AG, Otelfingen, Zurich, Switzerland.
Laboratory for Animal Model Pathology, Universität Zürich, Zurich, Switzerland.
Mol Cancer Ther. 2021 Mar;20(3):512-522. doi: 10.1158/1535-7163.MCT-20-0361. Epub 2020 Dec 22.
Small molecule-drug conjugates (SMDCs) represent an alternative to conventional antitumor chemotherapeutic agents, with the potential to improve the therapeutic window of cytotoxic payloads through active delivery at the site of the disease. In this article, we describe novel combination therapies consisting of anti-carbonic anhydrase IX SMDCs combined with different immunomodulatory products. The therapeutic effect of the SMDCs was potentiated by combination with PD-1 blockade and with tumor-homing antibody-cytokine fusions in mouse models of renal cell carcinoma and colorectal cancer. The combination with L19-IL12, a fusion protein specific to the alternatively spliced EDB domain of fibronectin containing the murine IL12 moiety, was also active against large established tumors. Analysis of the microscopic structures of healthy organs performed 3 months after tumor eradication confirmed absence of pathologic abnormalities in the healthy kidney, liver, lung, stomach, and intestine. Our findings may be of clinical significance as they provide motivation for the development of combinations based on SMDCs and immunotherapy for the treatment of renal cell carcinoma and hypoxic tumors.
小分子药物偶联物(SMDCs)是传统抗肿瘤化疗药物的一种替代选择,具有通过在疾病部位主动递送来改善细胞毒性载荷治疗窗口的潜力。在本文中,我们描述了由抗碳酸酐酶IX SMDCs与不同免疫调节产品组成的新型联合疗法。在肾细胞癌和结直肠癌小鼠模型中,SMDCs与PD - 1阻断剂以及肿瘤归巢抗体 - 细胞因子融合物联合使用时,其治疗效果得到增强。与L19 - IL12(一种含有鼠IL12部分的纤连蛋白可变剪接EDB结构域特异性融合蛋白)联合使用,对已形成的大肿瘤也有活性。在肿瘤根除3个月后对健康器官微观结构的分析证实,健康的肾脏、肝脏、肺、胃和肠道没有病理异常。我们的发现可能具有临床意义,因为它们为基于SMDCs和免疫疗法联合治疗肾细胞癌和缺氧肿瘤的开发提供了动力。