Giralt Sergio, Bensinger William, Goodman Mark, Podoloff Donald, Eary Janet, Wendt Richard, Alexanian Raymond, Weber Donna, Maloney David, Holmberg Leona, Rajandran Joseph, Breitz Hazel, Ghalie Richard, Champlin Richard
The University of Texas, MD Anderson Cancer Center, Houston, TX 77030-4006, USA.
Blood. 2003 Oct 1;102(7):2684-91. doi: 10.1182/blood-2002-10-3250. Epub 2003 May 1.
Holmium-166 1, 4, 7, 10-tetraazcyclododecane-1, 4, 7, 10-tetramethylenephosphonate (166Ho-DOTMP) is a radiotherapeutic that localizes specifically to the skeleton and can deliver high-dose radiation to the bone and bone marrow. In patients with multiple myeloma undergoing autologous hematopoietic stem cell transplantation two phase 1/2 dose-escalation studies of high-dose 166Ho-DOTMP plus melphalan were conducted. Patients received a 30 mCi (1.110 Gbq) tracer dose of 166Ho-DOTMP to assess skeletal uptake and to calculate a patient-specific therapeutic dose to deliver a nominal radiation dose of 20, 30, or 40 Gy to the bone marrow. A total of 83 patients received a therapeutic dose of 166Ho-DOTMP followed by autologous hematopoietic stem cell transplantation 6 to 10 days later. Of the patients, 81 had rapid and sustained hematologic recovery, and 2 died from infection before day 60. No grades 3 to 4 nonhematologic toxicities were reported within the first 60 days. There were 27 patients who experienced grades 2 to 3 hemorrhagic cystitis, only 1 of whom had received continuous bladder irrigation. There were 7 patients who experienced complications considered to be caused by severe thrombotic microangiopathy (TMA). No cases of severe TMA were reported in patients receiving in 166Ho-DOMTP doses lower than 30 Gy. Approximately 30% of patients experienced grades 2 to 4 renal toxicity, usually at doses targeting more than 40 Gy to the bone marrow. Complete remission was achieved in 29 (35%) of evaluable patients. With a minimum follow-up of 23 months, the median survival had not been reached and the median event-free survival was 22 months. 166Ho-DOTMP is a promising therapy for patients with multiple myeloma and merits further evaluation.
钬-166 1,4,7,10-四氮杂环十二烷-1,4,7,10-四亚甲基膦酸酯(166Ho-DOTMP)是一种放射治疗剂,可特异性定位于骨骼,并能向骨骼和骨髓输送高剂量辐射。在接受自体造血干细胞移植的多发性骨髓瘤患者中,开展了两项关于高剂量166Ho-DOTMP加美法仑的1/2期剂量递增研究。患者接受30毫居里(1.110吉贝可)的166Ho-DOTMP示踪剂量,以评估骨骼摄取情况,并计算针对患者的治疗剂量,从而向骨髓输送20、30或40戈瑞的标称辐射剂量。共有83例患者接受了166Ho-DOTMP治疗剂量,随后在6至10天后进行自体造血干细胞移植。这些患者中,81例实现了快速且持续的血液学恢复,2例在第60天前死于感染。在前60天内未报告3至4级非血液学毒性。有27例患者出现2至3级出血性膀胱炎,其中仅1例接受了持续膀胱冲洗。有7例患者出现被认为由严重血栓性微血管病(TMA)引起的并发症。接受低于30戈瑞166Ho-DOMTP剂量的患者中未报告严重TMA病例。约30%的患者出现2至4级肾毒性,通常发生在针对骨髓剂量超过40戈瑞时。29例(35%)可评估患者实现了完全缓解。在最短随访23个月时,中位生存期尚未达到,中位无事件生存期为22个月。166Ho-DOTMP对多发性骨髓瘤患者是一种有前景的治疗方法,值得进一步评估。