Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York.
Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Mol Cancer Ther. 2021 Nov;20(11):2189-2197. doi: 10.1158/1535-7163.MCT-21-0126. Epub 2021 Sep 4.
Limited clinical data are available regarding the utility of multikinase inhibition in neuroblastoma. Repotrectinib (TPX-0005) is a multikinase inhibitor that targets ALK, TRK, JAK2/STAT, and Src/FAK, which have all been implicated in the pathogenesis of neuroblastoma. We evaluated the preclinical activity of repotrectinib monotherapy and in combination with chemotherapy as a potential therapeutic approach for relapsed/refractory neuroblastoma. sensitivity to repotrectinib, ensartinib, and cytotoxic chemotherapy was evaluated in neuroblastoma cell lines. antitumor effect of repotrectinib monotherapy, and in combination with chemotherapy, was evaluated using a genotypically diverse cohort of patient-derived xenograft (PDX) models of neuroblastoma. Repotrectinib had comparable cytotoxic activity across cell lines irrespective of mutational status. Combination with chemotherapy demonstrated increased antiproliferative activity across several cell lines. Repotrectinib monotherapy had notable antitumor activity and prolonged event-free survival compared with vehicle and ensartinib in PDX models ( < 0.05). Repotrectinib plus chemotherapy was superior to chemotherapy alone in -mutant and wild-type PDX models. These results demonstrate that repotrectinib has antitumor activity in genotypically diverse neuroblastoma models, and that combination of a multikinase inhibitor with chemotherapy may be a promising treatment paradigm for translation to the clinic.
关于多激酶抑制在神经母细胞瘤中的应用,临床数据有限。Repotrectinib(TPX-0005)是一种多激酶抑制剂,靶向 ALK、TRK、JAK2/STAT 和 Src/FAK,这些激酶都与神经母细胞瘤的发病机制有关。我们评估了 Repotrectinib 单药治疗和联合化疗作为复发性/难治性神经母细胞瘤潜在治疗方法的临床前活性。在神经母细胞瘤细胞系中评估了 Repotrectinib、ensartinib 和细胞毒性化疗的敏感性。使用基因多样化的神经母细胞瘤患者来源异种移植(PDX)模型评估了 Repotrectinib 单药治疗和联合化疗的抗肿瘤作用。Repotrectinib 对细胞系的细胞毒性活性相似,与突变状态无关。联合化疗显示在几种细胞系中增殖活性增加。与载体和 ensartinib 相比,Repotrectinib 单药治疗在 PDX 模型中具有显著的抗肿瘤活性和延长的无事件生存期(<0.05)。Repotrectinib 联合化疗在-突变和野生型 PDX 模型中优于单独化疗。这些结果表明,Repotrectinib 在基因多样化的神经母细胞瘤模型中具有抗肿瘤活性,多激酶抑制剂联合化疗可能是一种有前途的治疗方案,可以转化为临床应用。