Zalutsky M R, Bigner D D
Department of Radiology, Duke University Medical Center, Durham, NC, USA.
Acta Oncol. 1996;35(3):373-9. doi: 10.3109/02841869609101654.
Radionuclides which decay by the emission of alpha-particles are attractive for certain radioimmunotherapeutic applications. These include the treatment of lymphomas, compartmentally spread malignancies such as ovarian cancer and neoplastic meningitis, and micrometastatic disease. Two alpha-emitting radionuclides of interest for this purpose are 212Bi (60.6 min half life) and 211At (7.2 hr half life). Compared with the beta-emitters commonly used for radiotherapy, the alpha-particles of 212Bi and 211At are of higher energy, much shorter range (less than 100 microm), and considerably higher linear energy transfer. Preliminary results obtained in a variety of in vitro systems and in vivo models have documented the exquisite toxicity of alpha-particles and have established a basis for initiating radiotherapy trials in humans with monoclonal antibodies labeled with alpha-emitting radionuclides.
通过发射α粒子衰变的放射性核素在某些放射免疫治疗应用中具有吸引力。这些应用包括治疗淋巴瘤、局部扩散的恶性肿瘤(如卵巢癌和肿瘤性脑膜炎)以及微转移疾病。为此目的,两种有吸引力的发射α粒子的放射性核素是212Bi(半衰期60.6分钟)和211At(半衰期7.2小时)。与常用于放射治疗的β发射体相比,212Bi和211At的α粒子能量更高、射程更短(小于100微米)且线能量转移显著更高。在各种体外系统和体内模型中获得的初步结果证明了α粒子具有极高的毒性,并为启动用发射α粒子的放射性核素标记的单克隆抗体进行人体放射治疗试验奠定了基础。