Phase I trial of iodine-131 tositumomab with high-dose chemotherapy and autologous stem-cell transplantation for relapsed non-Hodgkin's lymphoma

被引:115
作者
Vose, JM
Bierman, PJ
Enke, C
Hankins, J
Bociek, G
Lynch, JC
Armitage, JO
机构
[1] Univ Nebraska, Med Ctr, Hematol Oncol Sect, Omaha, NE 68198 USA
[2] Univ Nebraska, Med Ctr, Dept Radiat Oncol, Omaha, NE 68198 USA
[3] Univ Nebraska, Med Ctr, Dept Radiol, Omaha, NE 68198 USA
[4] Univ Nebraska, Med Ctr, Nucl Med Sect, Omaha, NE 68198 USA
[5] Univ Nebraska, Med Ctr, Dept Prevent & Societal Med, Omaha, NE 68198 USA
[6] Univ Nebraska, Med Ctr, Dept Internal Med, Omaha, NE 68198 USA
关键词
D O I
10.1200/JCO.2005.05.117
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To determine the maximum outpatient dose of iodine-131 tositumomab (up to 0.75 Gy) combined with high-dose carmustine, etoposide, cytarabine, and melphalan (BEAM) followed by autologous stem-cell transplantation (ASCT) for the treatment of Chemotherapy-resistant relapsed or refractory B-cell non-Hodgkin's lymphoma (NHL). Patients and Methods Twenty-three patients with chemotherapy-refractory or multiply-relapsed B-cell NHL were treated in a phase I trial combining iodine-131 tositumomab (ranging from 0.30 to 0.75 Gy total-body dose [TBD]) with high-dose BEAM followed by ASCT. Results The complete response rate after transplantation was 57%, and the overall response rate was 65%. Short-term and long-term toxicities were similar to historical control patients treated with BEAM alone. With a median follow-up of 38 months (range, 27 to 60 months), the overall survival (OS) rate was 55%, and the event-free survival (EFS) rate was 39%. Conclusion There were no significant added toxicities apparent with the addition of iodine-131 tositumomab up to a dose of 0.75 Gy TBD to high-dose BEAM chemotherapy followed by ASCT. The EFS and OS were encouraging in this group of chemotherapy-resistant or refractory B-cell NHL patients. A follow-up phase II trial with iodine-131 tositumomab at the dose of 0.75 Gy TBD with BEAM is currently ongoing. (C) 2005 by American Society of Clinical Oncology.
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页码:461 / 467
页数:7
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