Jhanwar Yuliya S, Divgi Chaitanya
Department of Radiology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
J Nucl Med. 2005 Jan;46 Suppl 1:141S-50S.
The recent approval of 2 radiolabeled antibodies against cluster designation 20-positive lymphoma has led to a resurgence of interest in radioimmunotherapy. As was the case with chemotherapy development, progress has been most marked in the hematologic neoplasms, both in myeloablative and in nonmyeloablative therapeutic strategies. Success in the radioimmunotherapy of solid tumors has lagged because of the immunogenicity of murine proteins and the relatively slow clearance of humanized intact immunoglobulins. Genetic engineering has enabled the development of a variety of antigen-binding constructs of various sizes and immunobiologic characteristics. Developments in radiochemistry as well as production of an increasing number of radionuclides with therapeutic potential or optimal imaging characteristics have spurred tailored therapeutic strategies that include dosimetry and considerations of tumor burden. Such progress has generated pivotal studies that will establish the radiobiologic paradigms for successful radioimmunotherapy of solid tumors. This review will describe seminal studies that have paved the way to an understanding of radioimmunotherapy in solid tumors. Finally, the authors' views of the future of this promising cancer therapy will be presented.
最近,2种针对簇分化抗原20阳性淋巴瘤的放射性标记抗体获得批准,这使得人们对放射免疫疗法的兴趣再度兴起。与化疗发展的情况一样,血液系统肿瘤在清髓性和非清髓性治疗策略方面的进展最为显著。实体瘤放射免疫治疗的成功滞后,原因在于鼠源蛋白的免疫原性以及人源化完整免疫球蛋白的清除相对缓慢。基因工程已促成了各种大小和免疫生物学特性的抗原结合构建体的开发。放射化学的发展以及越来越多具有治疗潜力或最佳成像特性的放射性核素的生产,推动了包括剂量测定和肿瘤负荷考量在内的定制治疗策略的发展。这些进展催生了一些关键研究,这些研究将确立实体瘤成功进行放射免疫治疗的放射生物学范式。本综述将描述为理解实体瘤放射免疫治疗铺平道路的开创性研究。最后,将呈现作者们对这种有前景的癌症治疗方法未来发展的看法。