Hassan Raffit, Alewine Christine, Pastan Ira
Laboratory of Molecular Biology, National Cancer Institute, NIH, Bethesda, Maryland. Thoracic and GI Oncology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Laboratory of Molecular Biology, National Cancer Institute, NIH, Bethesda, Maryland.
Clin Cancer Res. 2016 Mar 1;22(5):1055-8. doi: 10.1158/1078-0432.CCR-15-1623. Epub 2015 Oct 13.
Immunotoxins are targeted anticancer therapeutics that kill cancer cells using a cytotoxic bacterial toxin payload. Their development for use in solid tumor malignancies was delayed due to issues with their immunogenicity and limited therapeutic window. However, new research has rejuvenated the field. Coadministration with a lymphocyte-depleting regimen of pentostatin and cyclophosphamide can delay antidrug antibody formation, increasing the number of treatment cycles that patients can receive and resulting in durable responses in heavily pretreated patients. In addition, a new generation of immunotoxin molecules with reduced immunogenicity and nonspecific toxicity has been developed through protein engineering techniques, and one has recently entered the clinic. In preclinical studies in mouse models, these new agents are effective against many tumor types as single agents, and also produce synergistic antitumor responses in combination with chemotherapy. These new immunotoxins have renewed excitement in the field and may prove a promising addition to the targeted therapy repertoire.
免疫毒素是一种靶向抗癌治疗药物,它利用细胞毒性细菌毒素有效载荷来杀死癌细胞。由于其免疫原性问题和有限的治疗窗口,其在实体瘤恶性肿瘤中的应用开发有所延迟。然而,新的研究使该领域重获生机。与喷司他丁和环磷酰胺的淋巴细胞清除方案联合使用,可以延迟抗药抗体的形成,增加患者能够接受的治疗周期数,并在经过大量预处理的患者中产生持久反应。此外,通过蛋白质工程技术开发出了新一代免疫原性和非特异性毒性降低的免疫毒素分子,其中一种最近已进入临床。在小鼠模型的临床前研究中,这些新药物作为单一药物对多种肿瘤类型有效,并且与化疗联合使用时还能产生协同抗肿瘤反应。这些新型免疫毒素重新激发了该领域的热情,可能成为靶向治疗药物库中有前景的补充药物。