Brechbiel Martin W
Radioimmune & Inorganic Chemistry Section Radiation Oncology Branch, NCI, NIH Building 10, Room 1B40 10 Center Drive Bethesda, MD 20892-1088, USA.
Dalton Trans. 2007 Nov 21(43):4918-28. doi: 10.1039/b704726f. Epub 2007 Sep 11.
Monoclonal antibodies have become a viable strategy for the delivery of therapeutic, particle emitting radionuclides specifically to tumor cells to either augment anti-tumor action of the native antibodies or to solely take advantage of their action as targeting vectors. Proper and rational selection of radionuclide and antibody combinations is critical to making radioimmunotherapy (RIT) a standard therapeutic modality due to the fundamental and significant differences in the emission of either alpha- and beta-particles. The alpha-particle has a short path length (50-80 microm) that is characterized by high linear energy transfer (100 keV microm(-1)). Actively targeted alpha-therapy potentially offers a more specific tumor cell killing action with less collateral damage to the surrounding normal tissues than beta-emitters. These properties make targeted alpha-therapy an appropriate therapy to eliminate minimal residual or micrometastatic disease. RIT using alpha-emitters such as (213)Bi, (211)At, (225)Ac, and others has demonstrated significant activity in both in vitro and in vivo model systems. Limited numbers of clinical trials have progressed to demonstrate safety, feasibility, and therapeutic activity of targeted alpha-therapy, despite having to traverse complex obstacles. Further advances may require more potent isotopes, additional sources and more efficient means of isotope production. Refinements in chelation and/or radiolabeling chemistry combined with rational improvements of isotope delivery, targeting vectors, molecular targets, and identification of appropriate clinical applications remain as active areas of research. Ultimately, randomized trials comparing targeted alpha-therapy combined with integration into existing standards of care treatment regimens will determine the clinical utility of this modality.
单克隆抗体已成为一种可行的策略,可将治疗性、发射粒子的放射性核素特异性递送至肿瘤细胞,以增强天然抗体的抗肿瘤作用,或仅利用其作为靶向载体的作用。由于α粒子和β粒子发射存在根本且显著的差异,因此合理选择放射性核素和抗体组合对于使放射免疫疗法(RIT)成为标准治疗方式至关重要。α粒子的路径长度较短(50 - 80微米),其特征在于高线性能量传递(100 keV微米⁻¹)。与β发射体相比,主动靶向α疗法可能提供更具特异性的肿瘤细胞杀伤作用,对周围正常组织的附带损伤更小。这些特性使靶向α疗法成为消除微小残留或微转移疾病的合适疗法。使用诸如²¹³Bi、²¹¹At、²²⁵Ac等α发射体的RIT在体外和体内模型系统中均已显示出显著活性。尽管必须克服复杂障碍,但仍有数量有限的临床试验取得进展,证明了靶向α疗法的安全性、可行性和治疗活性。进一步的进展可能需要更有效的同位素、更多的来源以及更高效的同位素生产方法。螯合和/或放射性标记化学的改进,以及同位素递送、靶向载体、分子靶点的合理改进,以及确定合适的临床应用,仍然是活跃的研究领域。最终,比较靶向α疗法并将其纳入现有标准治疗方案的随机试验将确定这种治疗方式的临床效用。