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用于治疗恶性胶质瘤的转铁蛋白受体配体靶向毒素偶联物(Tf-CRM107)

Transferrin receptor ligand-targeted toxin conjugate (Tf-CRM107) for therapy of malignant gliomas.

作者信息

Weaver Michael, Laske Douglas W

机构信息

Department of Neurosurgery, Temple University School of Medicine, Philadelphia, PA 19140-5103, USA.

出版信息

J Neurooncol. 2003 Oct;65(1):3-13. doi: 10.1023/a:1026246500788.

Abstract

The authors review the preclinical and clinical results of the ligand-targeted toxin conjugate Transferrin-CRM107 (Tf-CRM107), for the treatment of malignant gliomas. Tf-CRM107 is a conjugate protein of diphtheria toxin with a point mutation (CRM107) linked by a thioester bond to human transferrin (Tf). This conjugate exhibits potent cytotoxicity in vitro against mammalian cells expressing the transferrin receptor with activity at picomolar concentrations. Phase I clinical trial results demonstrated that Tf-CRM107, delivered via a high-flow convection method utilizing stereotactically placed catheters, produced tumor response in patients with malignant brain tumors refractory to conventional therapy without severe neurologic or systemic toxicity. The results of a Phase II study are also summarized. Tf-CRM107 treatment results in complete and partial tumor response without severe toxicity in 35% of the evaluable patients. These data warrant a Phase III study as well as continued research in the field of targeted toxin therapy. Future directions of research include optimizing Tf-CRM107 delivery to targeted brain regions, and improving the treatment efficacy by combining with other toxin conjugates targeted to different receptors.

摘要

作者回顾了配体靶向毒素偶联物转铁蛋白-CRM107(Tf-CRM107)治疗恶性胶质瘤的临床前和临床结果。Tf-CRM107是一种白喉毒素的偶联蛋白,其具有一个点突变(CRM107),通过硫酯键与人转铁蛋白(Tf)相连。这种偶联物在体外对表达转铁蛋白受体的哺乳动物细胞具有强大的细胞毒性,在皮摩尔浓度下即有活性。I期临床试验结果表明,通过利用立体定向放置导管的高流量对流方法给药的Tf-CRM107,在对传统治疗难治的恶性脑肿瘤患者中产生了肿瘤反应,且无严重的神经或全身毒性。II期研究结果也进行了总结。Tf-CRM107治疗使35%的可评估患者出现了肿瘤完全缓解和部分缓解,且无严重毒性。这些数据为开展III期研究以及在靶向毒素治疗领域继续开展研究提供了依据。未来的研究方向包括优化Tf-CRM107向靶向脑区的递送,以及通过与其他靶向不同受体的毒素偶联物联合使用来提高治疗效果。

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