SAR3419: An Anti-CD19-Maytansinoid Immunoconjugate for the Treatment of B-Cell Malignancies

被引:124
作者
Blanc, Veronique [1 ]
Bousseau, Anne [1 ]
Caron, Anne [1 ]
Carrez, Chantal [1 ]
Lutz, Robert J. [2 ]
Lambert, John M. [2 ]
机构
[1] Sanofi, Oncol Business Div, F-94403 Vitry Sur Seine, France
[2] ImmunoGen Inc, Waltham, MA USA
关键词
NON-HODGKINS-LYMPHOMA; MONOCLONAL-ANTIBODY THERAPY; CHRONIC LYMPHOCYTIC-LEUKEMIA; PHASE-I; INOTUZUMAB OZOGAMICIN; ANTITUMOR-ACTIVITY; DRUG CONJUGATE; CANCER; RITUXIMAB; MAYTANSINE;
D O I
10.1158/1078-0432.CCR-11-0485
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
SAR3419 is a novel anti-CD19 humanized monoclonal antibody conjugated to a maytansine derivate through a cleavable linker for the treatment of B-cell malignancies. SAR3419 combines the strengths of a high-potency tubulin inhibitor and the exquisite B-cell selectivity of an anti-CD19 antibody. The internalization and processing of SAR3419, following its binding at the surface of CD19-positive human lymphoma cell lines and xenograft models, release active metabolites that trigger cell-cycle arrest and apoptosis, leading to cell death and tumor regression. SAR3419 has also been shown to be active in different lymphoma xenograft models, including aggressive diffuse large B-cell lymphoma, resulting in complete regressions and tumor-free survival. In these models, the activity of SAR3419 compared favorably with rituximab and lymphoma standard of care chemotherapy. Two phase I trials with 2 different schedules of SAR3419 as a single agent were conducted in refractory/relapsed B-cell non-Hodgkin lymphoma. Activity was reported in both schedules, in heavily pretreated patients of both follicular and diffuse large B-cell lymphoma subtypes, with a notable lack of significant hematological toxicity, validating SAR3419 as an effective antibody-drug conjugate and opening opportunities in the future. Numerous B-cell-specific anti-CD19 biologics are available to treat B-cell non-Hodgkin lymphoma, and early phase I results obtained with SAR3419 suggest that it is a promising candidate for further development in this disease. In addition, thanks to the broad expression of CD19, SAR3419 may provide treatment options for B-cell leukemias that are often CD20-negative. Clin Cancer Res; 17(20); 6448-58. (C) 2011 AACR.
引用
收藏
页码:6448 / 6458
页数:11
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