Yttrium 90-labeled ibritumomab tiuxetan radioimmunotherapy produces high response rates and durable remissions in patients with previously treated B-cell lymphoma

被引:94
作者
Gordon, LI
Witzig, T
Molina, A
Czuczman, M
Emmanouilides, C
Joyce, R
Vo, K
Theuer, C
Pohlman, B
Bartlett, N
Wiseman, G
Darif, M
White, C
机构
[1] Northwestern Univ, Feinberg Sch Med, Div Hematol Oncol, Chicago, IL 60611 USA
[2] Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[3] Mayo Clin & Mayo Fdn, Rochester, MN USA
[4] Biogen Idec Pharmaceut, San Diego, CA USA
[5] Roswell Pk Canc Ctr, Buffalo, NY USA
[6] Univ Calif Los Angeles, Div Hematol Oncol, Los Angeles, CA USA
[7] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[8] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[9] Washington Univ, Div Oncol, St Louis, MO USA
来源
CLINICAL LYMPHOMA | 2004年 / 5卷 / 02期
关键词
biodistribution; follicular lymphoma; non-Hodgkin s lymphoma; rituximab;
D O I
10.3816/CLM.2004.n.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We report updated time-to-event variables of a phase III randomized study comparing yttrium 90-labeled ibritumomab with rituximab Standard therapy in 143 rituximab-naive patients with relapsed or refractory low-grade, follicular, or transformed CD20(+) non-Hodgkin's lymphoma (NHL). Most patients (79%) had follicular lymphoma. Patients were randomized to receive a single intravenous (I.V.) dose of Y-90 ibritumomab tiuxetan 0.4 mCi/kg (n = 73) or rituximab 375 mg/m(2) I.V. weekly for 4 doses (n = 70). The radioimmunotherapy group was pretreated with 2 rituximab doses (250 mg/m(2)) to improve biodistribution and one dose of Indium 111-labeled ibritumornab tiuxetan for imaging. The overall response rate was 80% versus 56% (P= 0.002) and complete response (CR)/CR unconfirmed (CRu) rates were 34% for Y-90 ibritumomab tiuxetan versus 20% for rituximab. With a median follow-up of 44 months, the data are mature as all ongoing patients in both groups exceeded the median Kaplan-Meier estimated time to progression (TTP), duration of response (DR), and time to next therapy. Although this study was not powered to detect differences in time-to-event variables, the results from this randomized trial demonstrate trends toward longer median TTP (15 vs. 10.2 months; P= 0.07), DR (16.7 vs. 11.2 months; P= 0.44) and time to next therapy (21.1 vs. 13.8 months; P = 0.27) in follicular NHL patients treated with Y-90 ibritumomab tiuxetan compared with the rituximab control arm. In patients achieving a CR/CRu, the median TTP was 24.7 months for patients treated with Y-90 ibritumomab tiuxetan compared with 13.2 months for rituximab-treated patients (P = 0.41), and ongoing responses of > 5 years have been observed. These results confirm that Y-90 ibritumomab tiuxetan produces high response rates and durable remissions in patients with previously treated low-grade, follicular, and transformed NHL.
引用
收藏
页码:98 / 101
页数:4
相关论文
共 11 条
[1]   Subsequent chemotherapy regimens are well tolerated after radioimmunotherapy with yttrium-90 ibritumomab tiuxetan for non-Hodgkin's lymphoma [J].
Ansell, SM ;
Ristow, KM ;
Habermann, TM ;
Wiseman, GA ;
Witzig, TE .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (18) :3885-3890
[2]   Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas [J].
Cheson, BD ;
Horning, SJ ;
Coiffier, B ;
Shipp, MA ;
Fisher, RI ;
Connors, JM ;
Lister, TA ;
Vose, J ;
Grillo-López, A ;
Hagenbeek, A ;
Cabanillas, F ;
Klippensten, D ;
Hiddemann, W ;
Castellino, R ;
Harris, NL ;
Armitage, JO ;
Carter, W ;
Hoppe, R ;
Canellos, GP .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1244-1253
[3]  
Czuczman M, 2002, BLOOD, V100, p357A
[4]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481
[5]  
Knox SJ, 1996, CLIN CANCER RES, V2, P457
[6]  
SCHILDER RJ, 2002, P AN M AM SOC CLIN, V21, pA267
[7]   Ibritumomab tiuxetan radioimmunotherapy for patients with relapsed or refractory non-Hodgkin lymphoma and mild thrombocytopenia:: a phase II multicenter trial [J].
Wiseman, GA ;
Gordon, LI ;
Multani, PS ;
Witzig, TE ;
Spies, S ;
Bartlett, NL ;
Schilder, RJ ;
Murray, JL ;
Saleh, M ;
Allen, RS ;
Grillo-López, AJ ;
White, CA .
BLOOD, 2002, 99 (12) :4336-4342
[8]   Treatment with ibritumomab tiuxetan radioimmunotherapy in patients with rituximab-refractory follicular non-Hodgkin's lymphoma [J].
Witzig, TE ;
Flinn, IW ;
Gordon, LI ;
Emmanouilides, C ;
Czuczman, MS ;
Saleh, MN ;
Cripe, L ;
Wiseman, G ;
Olejnik, T ;
Multani, PS ;
White, CA .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (15) :3262-3269
[9]   Phase I/II trial of IDEC-Y2B8 radioimmunotherapy for treatment of relapsed or refractory CD20+ B-cell non-Hodgkin's lymphoma [J].
Witzig, TE ;
White, CA ;
Wiseman, GA ;
Gordon, LI ;
Emmanouilides, C ;
Raubitschek, A ;
Janakiraman, N ;
Gutheil, J ;
Schilder, RJ ;
Spies, S ;
Silverman, DHS ;
Parker, E ;
Grillo-López, AJ .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (12) :3793-3803
[10]   Safety of yttrium-90 ibritumomab tiuxetan radioimmunotherapy for relapsed low-grade, follicular, or transformed non-Hodgkin's lymphoma [J].
Witzig, TE ;
White, CA ;
Gordon, LI ;
Wiseman, GA ;
Emmanouilides, C ;
Murray, JL ;
Lister, J ;
Multani, PS .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (07) :1263-1270