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

被引:126
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
相关论文
共 60 条
[11]   Rituximab anti-CD20 monoclonal antibody therapy in non-Hodgkin's lymphoma:: Safety and efficacy of re-treatment [J].
Davis, TA ;
Grillo-López, AJ ;
White, CA ;
McLaughlin, P ;
Czuczman, MS ;
Link, BK ;
Maloney, DG ;
Weaver, RL ;
Rosenberg, J ;
Levy, R .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (17) :3135-3143
[12]   CD19 function in central and peripheral B-cell development [J].
Del Nagro, CJ ;
Otero, DC ;
Anzelon, AN ;
Omori, SA ;
Kolla, RV ;
Rickert, RC .
IMMUNOLOGIC RESEARCH, 2005, 31 (02) :119-131
[13]   REGULATORY ROLE OF CD19 MOLECULES IN B-CELL ACTIVATION AND DIFFERENTIATION [J].
DERIE, MA ;
SCHUMACHER, TNM ;
VANSCHIJNDEL, GMW ;
VANLIER, RAW ;
MIEDEMA, F .
CELLULAR IMMUNOLOGY, 1989, 118 (02) :368-381
[14]   Differential cellular internalization of anti-CD19 and-CD22 immunotoxins results in different cytotoxic activity [J].
Du, Xing ;
Beers, Richard ;
FitzGerald, David J. ;
Pastan, Ira .
CANCER RESEARCH, 2008, 68 (15) :6300-6305
[15]   Tumor Delivery and In Vivo Processing of Disulfide-Linked and Thioether-Linked Antibody-Maytansinoid Conjugates [J].
Erickson, Hans K. ;
Widdison, Wayne C. ;
Mayo, Michele F. ;
Whiteman, Kathleen ;
Audette, Charlene ;
Wilhelm, Sharon D. ;
Singh, Rajeeva .
BIOCONJUGATE CHEMISTRY, 2010, 21 (01) :84-92
[16]   Antibody-maytansinoid conjugates are activated in targeted cancer cells by lysosomal degradation and linker-dependent intracellular processing [J].
Erickson, HK ;
Park, PU ;
Widdison, WC ;
Kovtun, YV ;
Garrett, LM ;
Hoffman, K ;
Lutz, RJ ;
Goldmacher, VS ;
Blättler, WA .
CANCER RESEARCH, 2006, 66 (08) :4426-4433
[17]  
Erickson HK, 2009, P 100 ANN M AM ASS C, V69
[18]   Anti-CD30 Antibodies for Hodgkin Lymphoma [J].
Foyil, Kelley V. ;
Bartlett, Nancy L. .
CURRENT HEMATOLOGIC MALIGNANCY REPORTS, 2010, 5 (03) :140-147
[19]  
Fraser G, 2007, Curr Oncol, V14, P96
[20]   Diffuse Large B-Cell Lymphoma [J].
Friedberg, Jonathan W. ;
Fisher, Richard I. .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 2008, 22 (05) :941-+