Collins C, Eary J F, Donaldson G, Vernon C, Bush N E, Petersdorf S, Livingston R B, Gordon E E, Chapman C R, Appelbaum F R
Department of Medicine, University of Washington, Fred Hutchinson Cancer Research Center, Seattle.
J Nucl Med. 1993 Nov;34(11):1839-44.
Samarium-153-ethylenediaminetetramethylene phosphoric acid (EDTMP), a bone-seeking radiopharmaceutical, was given to prostate cancer patients in a dose escalation protocol for pain palliation to determine the maximally tolerated dose. Fifty-two patients with hormone refractory prostate cancer with bony metastases were treated with doses beginning at 0.5 mCi/kg (18.5 MBq/kg), escalating in 0.5-mCi (18.5 MBq) increments to 3.0 mCi/kg (111 MBq/kg). Pain response after treatment was assessed as well as hematologic and serum chemistry parameters. Pain palliation with a mean duration of 2.6 mo was present in 74% of the patients. Toxicity was exclusively hematologic at the highest dose levels. No infectious or bleeding complications occurred, with 45 of the 52 (86%) patients demonstrating complete hematologic recovery. Patients receiving higher doses had significantly greater reductions in serum prostate specific antigen and serum prostatic acid phosphatase levels. The patients receiving greater doses also showed a trend toward improved survival.
钐-153-乙二胺四亚甲基磷酸(EDTMP)是一种亲骨性放射性药物,在一项剂量递增方案中给予前列腺癌患者以缓解疼痛,从而确定最大耐受剂量。52例患有骨转移的激素难治性前列腺癌患者接受了治疗,起始剂量为0.5 mCi/kg(18.5 MBq/kg),以0.5 mCi(18.5 MBq)的增量递增至3.0 mCi/kg(111 MBq/kg)。评估了治疗后的疼痛反应以及血液学和血清化学参数。74%的患者出现了平均持续时间为2.6个月的疼痛缓解。在最高剂量水平时,毒性仅为血液学毒性。未发生感染或出血并发症,52例患者中有45例(86%)实现了完全血液学恢复。接受较高剂量的患者血清前列腺特异性抗原和血清前列腺酸性磷酸酶水平的降低更为显著。接受较大剂量的患者也显示出存活改善的趋势。