Effective therapy of murine models of human leukemia and lymphoma with radiolabeled anti-CD30 antibody, HeFi-1

被引:20
作者
Zhang, Meili
Yao, Zhengsheng
Patel, Hiral
Garmestani, Kayhan
Zhang, Zhuo
Talanov, Vladimir S.
Plascjak, Paul S.
Goldman, Carolyn K.
Janik, John E.
Brechbiel, Martin W.
Waldmann, Thomas A. [1 ]
机构
[1] NCI, Metab Branch, Ctr Canc Res, Bethesda, MD 20892 USA
[2] NCI, Radiat Oncol Branch, Ctr Canc Res, Bethesda, MD 20892 USA
[3] NIH, PET Dept, Clin Ctr, Bethesda, MD 20892 USA
[4] NCI, Lab Anim Sci Program, Ft Detrick, MD 21702 USA
[5] NCI, Appl Dev Res Support Program, Sci Applicat Int Corp, Frederick, MD 21702 USA
关键词
monoclonal antibody; radioimmunotherapy; alpha-emitter; beta-emitter;
D O I
10.1073/pnas.0702496104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
CD30 is a member of the TNF receptor superfamily. Overexpression of CD30 on some neoplasms versus limited expression on normal tissues makes this receptor a promising target for antibody-based therapy. Radioimmunotherapy of cancer with radiolabeled antibodies has shown promise. In this study, we evaluated the therapeutic efficacy of an anti-CD30 antibody, HeFi-1, armed with At-211 in a leukemia (karpas299) model and with Y-90 in a lymphoma (SUDHL-1) model. Furthermore, we investigated the combination therapy of At-211-HeFi-1 with unmodified HeFi-1 in the leukemia model. Treatment with unmodified HeFi-1 significantly prolonged the survival of the karpas299-bearing mice compared with the controls (P < 0.001). Treatment with At-211-HeFi-1 showed greater therapeutic efficacy than that with unmodified HeFi-1 as shown by survival of the mice (P < 0.001). Combining these two agents further improved the survival of the mice compared with the groups treated with either At-211-HeFi-1 (P < 0.05) or unmodified HeFi-1 (P < 0.001) alone. In the lymphoma model, the survival of the SUDHL-1-bearing mice was significantly prolonged by the treatment with Y-90-HeFi-1 compared with the controls (P < 0.001). In summary, radiolabeled HeFi-1 is very promising for the treatment of CD30-expressing leukemias and lymphomas, and the combination regimen of At-211-HeFi-1 with unmodified HeFi-1 enhanced the therapeutic efficacy.
引用
收藏
页码:8444 / 8448
页数:5
相关论文
共 47 条
[1]   The human anti-CD30 antibody 5F11 shows in vitro and in vivo activity against malignant lymphoma [J].
Borchmann, P ;
Treml, JF ;
Hansen, H ;
Gottstein, C ;
Schnell, R ;
Staak, O ;
Zhang, HF ;
Davis, T ;
Keler, T ;
Diehl, V ;
Graziano, RF ;
Engert, A .
BLOOD, 2003, 102 (10) :3737-3742
[2]   INDICATIONS FOR AUTOLOGOUS BONE-MARROW TRANSPLANTATION IN HODGKINS-DISEASE [J].
CARELLA, AM .
LEUKEMIA & LYMPHOMA, 1992, 7 :21-22
[3]   Discovering the neural basis of human social anxiety: A diagnostic and therapeutic imperative [J].
Charney, DS .
AMERICAN JOURNAL OF PSYCHIATRY, 2004, 161 (01) :1-2
[4]   CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma. [J].
Coiffier, B ;
Lepage, E ;
Brière, J ;
Herbrecht, R ;
Tilly, H ;
Bouabdallah, R ;
Morel, P ;
Van den Neste, E ;
Salles, G ;
Gaulard, P ;
Reyes, F ;
Gisselbrecht, C .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (04) :235-242
[5]  
DEBRUIN PC, 1995, LEUKEMIA, V9, P1620
[6]  
Dürkop H, 2000, J PATHOL, V190, P613
[7]  
Higgins JP, 1999, AM J CLIN PATHOL, V112, P241
[8]   CD30-mediated cell cycle arrest associated with induced expression of p21CIP1/WAF1 in the anaplastic large cell lymphoma cell line Karpas 299 [J].
Hübinger, G ;
Müller, E ;
Scheffrahn, I ;
Schneider, C ;
Hildt, E ;
Singer, BB ;
Sigg, I ;
Graf, J ;
Bergmann, L .
ONCOGENE, 2001, 20 (05) :590-598
[9]   Treatment of primary progressive Hodgkin's and aggressive non-Hodgkin's lymphoma: Is there a chance for cure? [J].
Josting, A ;
Reiser, M ;
Rueffer, U ;
Salzberger, B ;
Diehl, V ;
Engert, A .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (02) :332-339
[10]   Targeted at particle immunotherapy for myeloid leukemia [J].
Jurcic, JG ;
Larson, SM ;
Sgouros, G ;
McDevitt, MR ;
Finn, RD ;
Divgi, CR ;
Ballangrud, ÅM ;
Hamacher, KA ;
Ma, DS ;
Humm, JL ;
Brechbiel, MW ;
Molinet, R ;
Scheinberg, DA .
BLOOD, 2002, 100 (04) :1233-1239