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Cabozantinib for relapsed neuroblastoma: Single institution case series.卡博替尼治疗神经母细胞瘤复发:单机构病例系列。
Pediatr Blood Cancer. 2020 Jul;67(7):e28317. doi: 10.1002/pbc.28317. Epub 2020 Apr 28.
2
Repotrectinib (TPX-0005), effectively reduces growth of ALK driven neuroblastoma cells.Repotrectinib(TPX-0005)能有效抑制 ALK 驱动的神经母细胞瘤细胞的生长。
Sci Rep. 2019 Dec 18;9(1):19353. doi: 10.1038/s41598-019-55060-7.
3
Repotrectinib (TPX-0005) Is a Next-Generation ROS1/TRK/ALK Inhibitor That Potently Inhibits ROS1/TRK/ALK Solvent- Front Mutations.Repotrectinib(TPX-0005)是一种下一代 ROS1/TRK/ALK 抑制剂,能够强力抑制 ROS1/TRK/ALK 溶剂前沿突变。
Cancer Discov. 2018 Oct;8(10):1227-1236. doi: 10.1158/2159-8290.CD-18-0484. Epub 2018 Aug 9.
4
Novel Src/Abl tyrosine kinase inhibitor bosutinib suppresses neuroblastoma growth via inhibiting Src/Abl signaling.新型Src/Abl酪氨酸激酶抑制剂博舒替尼通过抑制Src/Abl信号传导来抑制神经母细胞瘤的生长。
Oncotarget. 2017 Jan 3;8(1):1469-1480. doi: 10.18632/oncotarget.13643.
5
The ALK inhibitor PF-06463922 is effective as a single agent in neuroblastoma driven by expression of ALK and MYCN.ALK抑制剂PF-06463922作为单一药物对由ALK和MYCN表达驱动的神经母细胞瘤有效。
Dis Model Mech. 2016 Sep 1;9(9):941-52. doi: 10.1242/dmm.024448. Epub 2016 Jul 7.
6
ALK inhibitor resistance in ALK(F1174L)-driven neuroblastoma is associated with AXL activation and induction of EMT.在ALK(F1174L)驱动的神经母细胞瘤中,ALK抑制剂耐药与AXL激活和上皮-间质转化的诱导有关。
Oncogene. 2016 Jul 14;35(28):3681-91. doi: 10.1038/onc.2015.434. Epub 2015 Nov 30.
7
High-throughput screening using patient-derived tumor xenografts to predict clinical trial drug response.利用患者来源的肿瘤异种移植物进行高通量筛选,以预测临床试验药物反应。
Nat Med. 2015 Nov;21(11):1318-25. doi: 10.1038/nm.3954. Epub 2015 Oct 19.
8
Crizotinib Synergizes with Chemotherapy in Preclinical Models of Neuroblastoma.克唑替尼在神经母细胞瘤临床前模型中与化疗协同作用。
Clin Cancer Res. 2016 Feb 15;22(4):948-60. doi: 10.1158/1078-0432.CCR-15-0379. Epub 2015 Oct 5.
9
Advances in Risk Classification and Treatment Strategies for Neuroblastoma.神经母细胞瘤风险分类与治疗策略的进展
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10
Targeting JAK kinase in solid tumors: emerging opportunities and challenges.靶向实体瘤中的JAK激酶:新出现的机遇与挑战。
Oncogene. 2016 Feb 25;35(8):939-51. doi: 10.1038/onc.2015.150. Epub 2015 May 18.

神经母细胞瘤中瑞波替尼的转化策略。

Translational Strategies for Repotrectinib in Neuroblastoma.

机构信息

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.

出版信息

Mol Cancer Ther. 2021 Nov;20(11):2189-2197. doi: 10.1158/1535-7163.MCT-21-0126. Epub 2021 Sep 4.

DOI:10.1158/1535-7163.MCT-21-0126
PMID:34482287
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8571000/
Abstract

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.

摘要

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。