Antilymphoma treatments given subsequent to yttrium 90 ibritumomab tiuxetan are feasible in patients with progressive non-Hodgkin's lymphoma: A review of the literature

被引:26
作者
Ansell, SM
Schilder, RJ
Pieslor, PC
Gordon, LI
Emmanouilides, C
Vo, K
Czuczman, MS
Witzig, TE
Theuer, C
Molina, A
机构
[1] Mayo Clin & Mayo Fdn, Div Hematol, Div Hematol Res, Rochester, MN 55905 USA
[2] Fox Chase Canc Ctr, Dept Med Oncol, Philadelphia, PA 19111 USA
[3] Biogen Idec, Cambridge, MA USA
[4] Northwestern Univ, Div Hematol Oncol, Chicago, IL 60611 USA
[5] Univ Calif Los Angeles, Div Hematol Oncol, Los Angeles, CA USA
[6] Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
来源
CLINICAL LYMPHOMA | 2004年 / 5卷 / 03期
关键词
chemotherapy; radioimmunotherapy; rituximab;
D O I
10.3816/CLM.2004.n.028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Yttrium 90-labeled ibritumomab tiuxetan is approved for the treatment of patients with relapsed or refractory low-grade, follicular, or transformed B-cell non-Hodgkin's lymphoma (NHL). To date, the efficacy of repeated courses of radioimmunoconjugate treatment in patients whose disease has progressed has not been studied as a formal endpoint in a clinical trial setting. However, several clinical studies have been conducted in patients with progressive NHL who had previously received (90)gamma ibritumomab tiuxetan. A retrospective review of these studies has shown that clinical responses have been achieved with all types of subsequent treatment with no apparent impact on their efficacy. In addition, no significant differences in toxicities with subsequent therapies have been observed between patients who had previously received (90)gamma ibritumomab tiuxetan therapy and those who had not. These findings suggest that patients previously treated with 90Y ibritumomab tiuxetan can feasibly undergo other forms of treatment for progressive NHL, and that a clinical response to further treatment options is not precluded by administration of (90)gamma ibriturnomab tiuxetan.
引用
收藏
页码:202 / 204
页数:3
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