Kennel S J, Mirzadeh S
Life Sciences Division, Oak Ridge National Laboratory, TN 37831-8080, USA.
Nucl Med Biol. 1998 Apr;25(3):241-6. doi: 10.1016/s0969-8051(97)00200-x.
To destroy both tumor blood vessels and adjacent tumor cells, an alpha-particle emitter, 213Bi, has been targeted with a monoclonal antibody (MAb) to vessels that feed lung tumors in mice. Animals, bearing approximately 100 EMT-6 carcinomas each of 50-400 cells in size in the lung, that were treated with 120 muCi of 213Bi-MAb 201B were all cured of their disease. Animals treated when tumors were larger (10(3)-10(4) cells) had extended life spans, but a small number of residual tumors eventually killed the animals. Significant extension of life span was also induced with another tumor model-rat tracheal carcinoma growing in the lungs of SCID mice that were then treated with 136 muCi 213Bi-MAb 201B. These studies indicate that attack of both blood vessels and tumor cells simultaneously is an effective mode of cancer treatment.
为了破坏肿瘤血管和邻近的肿瘤细胞,一种α粒子发射体213Bi已与一种单克隆抗体(MAb)结合,该单克隆抗体靶向为小鼠肺部肿瘤供血的血管。每只肺部带有约100个大小为50 - 400个细胞的EMT - 6癌的动物,用120微居里的213Bi - MAb 201B进行治疗后,所有动物的疾病均被治愈。在肿瘤较大(10³ - 10⁴个细胞)时接受治疗的动物寿命延长,但仍有少量残留肿瘤最终导致动物死亡。在另一种肿瘤模型——生长于SCID小鼠肺部的大鼠气管癌模型中,用136微居里的213Bi - MAb 201B进行治疗后,也显著延长了动物寿命。这些研究表明,同时攻击血管和肿瘤细胞是一种有效的癌症治疗方式。