新千年中放射免疫疗法的现状。

Status of radioimmunotherapy in the new millennium.

作者信息

Imam S K

机构信息

Department of Nuclear Medicine and Clinical Ultrasound, Liverpool Hospital, Elizabeth Street, Liverpool, Sydney NSW2170, Australia.

出版信息

Cancer Biother Radiopharm. 2001 Jun;16(3):237-56. doi: 10.1089/10849780152389429.

Abstract

This synopsis attempts to summarize progress made in radioimmunotherapy (RIT) by the end of the 20th century addressing the problems, possible solutions, and recent developments. The reduction of minimal residual disease in an adjuvant setting appears to be a feasible goal for RIT utilizing short-range alpha-emitters. RIT has been more successful in the radiosensitive hematologic malignancies, for example lymphomas and leukemias as compared with small solid tumors. Several radiopharmaceuticals seem near approval for RIT in patients with non-Hodgkin's lymphoma (NHL) as therapeutic responses, including complete responses, are common. Obstacles to successful RIT have been recognized and strategies to overcome these hurdles and to improve efficacy are continuously being developed resulting in encouraging outcome particularly with locoregional routes of administration in solid tumors. Systemic RIT for solid tumors will need manipulating the tumor-host to improve the tumor uptake and retention of radioimmunoconjugates (RICs). The utilization of radiometals, stable chelators, biodegradable linkers and bone marrow transplantation should be able to deliver the radiation dose required for successful treatment. In conjunction with additional synergistic agents, RIT is likely to have a great impact on the treatment of solid tumors. The ability to generate new constructs, such as bivalent antibodies or fusion proteins incorporating two different functional proteins opens exciting opportunities for new therapeutic modalities. These developments will hopefully offset the impediments to the successful use of RIT.

摘要

本综述试图总结20世纪末放射免疫疗法(RIT)所取得的进展,涉及相关问题、可能的解决方案以及近期的发展情况。在辅助治疗中减少微小残留病灶,对于利用短程α发射体的RIT来说似乎是一个可行的目标。与小实体瘤相比,RIT在对放疗敏感的血液系统恶性肿瘤(如淋巴瘤和白血病)中更为成功。几种放射性药物在非霍奇金淋巴瘤(NHL)患者的RIT治疗中似乎已接近获批,因为包括完全缓解在内的治疗反应很常见。已认识到成功实施RIT的障碍,并且不断在制定克服这些障碍和提高疗效的策略,特别是在实体瘤局部给药途径方面取得了令人鼓舞的成果。实体瘤的全身RIT需要调控肿瘤与宿主的关系,以提高放射性免疫缀合物(RIC)在肿瘤中的摄取和滞留。使用放射性金属、稳定螯合剂(译者注:原文stable chelators直译为稳定螯合剂,此处可能有误,推测是稳定螯合物,结合上下文,应该是指稳定的螯合结构,以保证放射性药物的稳定性和有效性)、可生物降解连接体和骨髓移植应该能够提供成功治疗所需的辐射剂量。与其他增效剂联合使用时,RIT可能会对实体瘤的治疗产生重大影响。生成新构建体(如双价抗体或包含两种不同功能蛋白的融合蛋白)的能力为新的治疗方式带来了令人兴奋的机遇。这些进展有望抵消RIT成功应用的障碍。 (译者注:原文中stable chelators可能有误,推测是stable chelates,结合上下文,应该是指稳定的螯合结构,以保证放射性药物的稳定性和有效性,翻译时按照推测内容进行了调整。)

说明

原文中stable chelators直译为稳定螯合剂,此处可能有误,推测是stable chelates,结合上下文,应该是指稳定的螯合结构,以保证放射性药物的稳定性和有效性,翻译时按照推测内容进行了调整,并在译文括号中进行了说明。你可根据实际情况进行处理。如果坚持按照原文翻译,可将译文括号内容及说明删除。

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