Drugs R D. 2005;6(1):49-52. doi: 10.2165/00126839-200506010-00006.
Glufosfamide [D 19575, beta-D-Glc-IPM] is a next-generation glucose conjugate of ifosfamide that is under development with Threshold Pharmaceuticals for the treatment of cancer. It is an alkylating agent in which isophosphoramide mustard, the alkylating metabolite of ifosfamide, is glycosidically linked to beta-D-glucose. Cellular uptake of glufosfamide is mediated by a sodium-dependent transmembrane transporter protein of glucose and possibly also by other transporter proteins. Threshold is using its Metabolic Targeting technology to exploit unique aspects of tumour metabolism, particularly the elevated glucose utilisation of tumour cells to selectively target glufosfamide to the tumour site. Glufosfamide was originally developed from a research collaboration between Asta Medica (Degussa) and the Cancer Research Centre (DKFZ) in Heidelberg, Germany. In October 2001, Baxter International acquired the oncology division of ASTA Medica, and renamed it Baxter Oncology GmbH. According to its 2002 Annual Report, Baxter announced that it was terminating development of glufosfamide. Subsequently, Baxter and Threshold Pharmaceuticals entered into an exclusive licensing and development agreement in August 2003. Threshold has responsibility for the development and commercialisation of glufosfamide, primarily for use as an antitumour agent. In addition, Baxter manufactures glufosfamide on Threshold's behalf. Threshold received fast-track status for glufosfamide from the US FDA in the treatment of metastatic pancreatic cancer refractory to gemcitabine in November 2004. In December 2004, Threshold initiated a phase I/II trial (TH-CR-301 Study) investigating glufosfamide in combination with gemcitabine as a first-line treatment of pancreatic cancer or advanced solid tumours. The phase I portion of the study may enroll up to 15 patients. The maximum tolerable dose combination determined will then be used in the phase 2 portion of the study. Up to 42 patients with advanced pancreatic cancer will be enrolled at various sites in the US, Latin America and Brazil.Previously, glufosfamide had been in phase II trials among patients with pancreatic carcinoma in Germany with Baxter Oncology and with the EORTC in the UK as well as Greece. However, development has been discontinued.
葡磷酰胺[D 19575,β-D-葡萄糖-异环磷酰胺]是异环磷酰胺的新一代葡萄糖偶联物,正由Threshold制药公司进行开发用于癌症治疗。它是一种烷化剂,其中异环磷酰胺的烷化代谢物异环磷酰胺氮芥通过糖苷键与β-D-葡萄糖相连。葡磷酰胺的细胞摄取由葡萄糖的钠依赖性跨膜转运蛋白介导,也可能由其他转运蛋白介导。Threshold公司正在利用其代谢靶向技术来利用肿瘤代谢的独特方面,特别是肿瘤细胞对葡萄糖利用率的提高,以将葡磷酰胺选择性地靶向肿瘤部位。葡磷酰胺最初是由德国海德堡的阿斯塔制药公司(德固赛)与癌症研究中心(德国癌症研究中心)合作研发的。2001年10月,百特国际收购了阿斯塔制药公司的肿瘤学部门,并将其更名为百特肿瘤有限公司。根据其2002年年度报告,百特宣布终止葡磷酰胺的开发。随后,百特与Threshold制药公司于2003年8月达成了一项独家许可和开发协议。Threshold公司负责葡磷酰胺的开发和商业化,主要用作抗肿瘤药物。此外,百特代表Threshold公司生产葡磷酰胺。2004年11月,Threshold公司的葡磷酰胺获得了美国食品药品监督管理局的快速通道地位,用于治疗对吉西他滨耐药的转移性胰腺癌。2004年12月,Threshold公司启动了一项I/II期试验(TH-CR-301研究),研究葡磷酰胺联合吉西他滨作为胰腺癌或晚期实体瘤的一线治疗方案。该研究的I期部分最多可招募15名患者。确定的最大耐受剂量组合将用于该研究的II期部分。美国、拉丁美洲和巴西的多个地点将招募多达42名晚期胰腺癌患者。此前,葡磷酰胺在德国曾与百特肿瘤公司以及在英国和希腊与欧洲癌症研究与治疗组织合作,在胰腺癌患者中进行II期试验。然而,该研发已停止。