Allen Barry J, Raja Chand, Rizvi Syed, Song Emma Y, Graham Peter
Phys Med Biol. 2007 Jul 7;52(13):L15-9. doi: 10.1088/0031-9155/52/13/L01. Epub 2007 Jun 7.
Targeted alpha therapy (TAT) is an emerging therapeutic modality, thought to be best suited to cancer micrometastases, leukaemia and lymphoma. TAT has not been indicated for solid tumours. However, several melanoma patients in a phase 1 clinical trial of systemic targeted alpha therapy for melanoma experienced marked regression of subcutaneous and internal tumours. This response cannot be ascribed to killing of all cancer cells in the tumours by targeted alpha therapy. These new observations support the original hypothesis that tumours can be regressed by a mechanism called tumour anti-vascular alpha therapy. This effect depends on the expression of targeted receptors by capillary pericytes and contiguous cancer cells, and on the short-range and high-energy transfer of alpha radiation.
靶向α治疗(TAT)是一种新兴的治疗方式,被认为最适用于癌症微转移、白血病和淋巴瘤。TAT尚未被用于实体瘤。然而,在一项针对黑色素瘤的全身靶向α治疗的1期临床试验中,几名黑色素瘤患者的皮下和体内肿瘤出现了明显消退。这种反应不能归因于靶向α治疗杀死了肿瘤中的所有癌细胞。这些新观察结果支持了最初的假设,即肿瘤可以通过一种称为肿瘤抗血管α治疗的机制消退。这种效应取决于毛细血管周细胞和相邻癌细胞对靶向受体的表达,以及α辐射的短程和高能传递。