Synergy of sequential administration of a deglycosylated ricin A chain-containing combined anti-CD19 and anti-CD22 immunotoxin (Combotox) and cytarabine in a murine model of advanced acute lymphoblastic leukemia

被引:24
作者
Barta, Stefan K. [1 ]
Zou, Yiyu [1 ]
Schindler, John [2 ,3 ]
Shenoy, Niraj [4 ]
Bhagat, Tushar D. [1 ]
Steidl, Ulrich [1 ]
Verma, Amit [1 ]
机构
[1] Albert Einstein Canc Ctr, Bronx, NY USA
[2] Univ Texas SW Med Ctr Dallas, Ctr Canc Immunobiol, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Microbiol, Dallas, TX 75390 USA
[4] Jacobi Med Ctr, Bronx, NY USA
关键词
Leukemia; acute lymphoblastic; immunoconjugate; cytarabine; ricin; animal model; mouse; NOD; B-CELL LYMPHOMA; CHEMOTHERAPY PLUS RITUXIMAB; RANDOMIZED CONTROLLED-TRIAL; ADULT BURKITT-LYMPHOMA; MONOCLONAL-ANTIBODIES; PHASE-I; COMBINATION; CD22; MICE; PRECURSOR;
D O I
10.3109/10428194.2012.679267
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The outcome for patients with refractory or relapsed acute lymphoblastic leukemia (ALL) treated with conventional therapy is poor. Immunoconjugates present a novel approach and have recently been shown to have efficacy in this setting. Combotox is a mixture of two ricin-conjugated monoclonal antibodies (RFB4 and HD37) directed against CD19 and CD22, respectively, and has shown activity in pediatric and adult ALL. We created a murine xenograft model of advanced ALL using the NALM/6 cell line to explore whether the combination of Combotox with the cytotoxic agent cytarabine (Ara-C) results in better outcomes. In our model the combination of both low-and high-dose Combotox and Ara-C resulted in significantly longer median survival. Sequential administration of Ara-C and Combotox, however, was shown to be superior to concurrent administration. These findings have led to a phase I clinical trial exploring this combination in adults with relapsed or refractory B-lineage ALL (ClinicalTrials.gov identifier NCT01408160).
引用
收藏
页码:1999 / 2003
页数:5
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