Goldenberg David M
Garden State Cancer Center, Center for Molecular Medicine and Immunology, Belleville, New Jersey 07109, USA.
J Nucl Med. 2002 May;43(5):693-713.
This review focuses on the use of radiolabeled antibodies in the therapy of cancer, termed radioimmunotherapy (RAIT). Basic problems concerning the choice of antibody and radionuclide and the physiology of tumor and host are discussed. Then follows a review of pertinent clinical publications on various radioantibody constructs in the treatment of hematopoietic and solid tumors of diverse histopathologies, grades, and stages, and in different clinical settings. Factors such as dose rate delivered, tumor size, and radiosensitivity play a major role in determining therapeutic response, while target-to-nontarget ratios and, particularly, circulating radioactivity to the bone marrow determine the major dose-limiting toxicities. RAIT appears to be gaining a place in the therapy of hematopoietic neoplasms, such as non-Hodgkin's lymphoma, with several agents advancing in clinical trials toward registration, of which one has just been approved by the FDA. Although RAIT of solid tumors has shown less progress, pretargeting strategies, such as an affinity-enhancement system consisting of bispecific antibodies separating targeting from delivery of the radiotherapeutic, appear to enhance tumor-to-nontumor ratios and may increase rad doses to tumor more selectively than directly labeled antibodies.
本综述聚焦于放射性标记抗体在癌症治疗中的应用,即放射免疫疗法(RAIT)。讨论了有关抗体和放射性核素选择以及肿瘤与宿主生理学的基本问题。接着回顾了关于各种放射性抗体构建体在治疗不同组织病理学、分级和分期的造血系统肿瘤及实体瘤,以及在不同临床环境中的相关临床出版物。诸如所给予的剂量率、肿瘤大小和放射敏感性等因素在决定治疗反应中起主要作用,而靶与非靶比值,尤其是骨髓中的循环放射性则决定了主要的剂量限制性毒性。放射免疫疗法似乎在造血系统肿瘤(如非霍奇金淋巴瘤)的治疗中逐渐占据一席之地,有几种药物在临床试验中朝着获批方向推进,其中一种刚刚获得美国食品药品监督管理局(FDA)的批准。尽管实体瘤的放射免疫疗法进展较小,但预靶向策略,如由双特异性抗体组成的亲和力增强系统(将靶向与放射治疗的递送分开),似乎能提高肿瘤与非肿瘤的比值,并且可能比直接标记抗体更有选择性地增加肿瘤的放射剂量。