Bierman P J, Vose J M, Leichner P K, Quadri S M, Armitage J O, Klein J L, Abrams R A, Dicke K A, Vriesendorp H M
Department of Internal Medicine, University of Nebraska Medical Center, Omaha 68198-3330.
J Clin Oncol. 1993 Apr;11(4):698-703. doi: 10.1200/JCO.1993.11.4.698.
This study was undertaken to examine the feasibility of combining radiolabeled antibody therapy with high-dose chemotherapy followed by autologous bone marrow transplantation in patients with poor-prognosis Hodgkin's disease.
Patients were entered onto this protocol if they had chemotherapy-resistant disease, bulky disease, or extensive prior therapy. Patients received yttrium-labeled antiferritin on day -13, -12, or -11, followed by high-dose cyclophosphamide, carmustine, and etoposide (CBV) on days -6 to -3, and then bone marrow infusion on day 0.
Twelve patients received both radiolabeled antibody and high-dose chemotherapy followed by autologous transplantation. Two additional patients started the study, but were unable to complete all therapy. Four of 12 patients experienced early transplant-related mortality. Four patients are alive more than 2 years following transplantation and three are free from disease progression at 24+, 25+, and 28+ months following transplantation. The progression-free survival rate at 1 year is estimated to be 21%. Considering the poor prognostic characteristics of these patients, toxicity on this protocol was not necessarily greater than that observed with high-dose chemotherapy alone.
This report demonstrates the feasibility of combining radiolabeled antibody therapy with high-dose chemotherapy and autologous bone marrow transplantation.
本研究旨在探讨对预后不良的霍奇金病患者,将放射性标记抗体治疗与大剂量化疗及随后的自体骨髓移植相结合的可行性。
有化疗抵抗性疾病、大块病灶或既往接受过广泛治疗的患者进入本方案。患者在第-13、-12或-11天接受钇标记的抗铁蛋白,随后在第-6至-3天接受大剂量环磷酰胺、卡莫司汀和依托泊苷(CBV),然后在第0天进行骨髓输注。
12例患者接受了放射性标记抗体和大剂量化疗并随后进行自体移植。另外2例患者开始了研究,但未能完成所有治疗。12例患者中有4例经历了早期移植相关死亡。4例患者移植后存活超过2年,3例在移植后24+、25+和28+个月时无疾病进展。估计1年无进展生存率为21%。考虑到这些患者预后不良的特征,本方案的毒性不一定大于单独大剂量化疗所观察到的毒性。
本报告证明了将放射性标记抗体治疗与大剂量化疗及自体骨髓移植相结合的可行性。