Anti-B-Cell Maturation Antigen BiTE Molecule AMG 420 Induces Responses in Multiple Myeloma

被引:251
作者
Topp, Max S. [1 ]
Duell, Johannes [1 ]
Zugmaier, Gerhard [2 ]
Attal, Michel [3 ]
Moreau, Philippe [4 ]
Langer, Christian [5 ]
Kroenke, Jan [6 ]
Facon, Thierry [7 ]
Salnikov, Alexey V. [8 ]
Lesley, Robin [9 ]
Beutner, Karl [10 ]
Kalabus, James [9 ]
Rasmussen, Erik [10 ]
Riemann, Kathrin [8 ]
Minella, Alex C. [10 ]
Munzert, Gerd [8 ]
Einsele, Hermann [1 ]
机构
[1] Univ Hosp Wurzburg, Dept Internal Med 2, Wurzburg, Germany
[2] Amgen Res Munich, Munich, Germany
[3] Univ Toulouse, Toulouse, France
[4] Univ Hosp Ctr Nantes, Hematol Dept, Nantes, France
[5] Kempten Clin, Kempten, Germany
[6] Ulm Univ, Ulm, Germany
[7] Reg Univ Hosp Lille, Lille, France
[8] Boehringer Ingelheim GmbH & Co KG, Biberach, Germany
[9] Amgen Inc, San Francisco, CA USA
[10] Amgen Inc, Thousand Oaks, CA USA
关键词
BCMA GENE; THERAPY;
D O I
10.1200/JCO.19.02657
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE The anti-B-cell maturation antigen BiTE molecule AMG 420 was assessed in patients with relapsed/refractory multiple myeloma. PATIENTS AND METHODS In this first-in-human study, up to 10 cycles of AMG 420 were given (4-week infusions/6-week cycles). Patients had progression after >= 2 lines of prior therapy and no extramedullary disease. Minimal residual disease (MRD) response was defined as < 1 tumor cell/10(4) bone marrow cells by flow cytometry. RESULTS Forty-two patients received AMG 420 at 0.2-800 mu g/d. Median age was 65 years, and median disease duration was 5.2 years. Median exposure was 1 cycle (range, 1-10 cycles) and 7 cycles (range, 1-10 cycles) for responders. Patients discontinued for disease progression (n = 25), adverse events (AEs; n = 7), death (n = 4), completion of 10 cycles (n = 3), and consent withdrawal (n = 1). Two patients remain on treatment. There were 2 nontreatment-related deaths from AEs, influenza/aspergillosis and adenovirus-related hepatitis. Serious AEs (n = 20; 48%) included infections (n = 14) and polyneuropathy (n = 2); treatment-related serious AEs included 2 grade 3 polyneuropathies and 1 grade 3 edema. There were no grade >= 3 CNS toxicities or anti-AMG 420 antibodies. In this study, 800 mu g/d was considered to not be tolerable because of 1 instance each of grade 3 cytokine release syndrome and grade 3 polyneuropathy, both of which resolved. The overall response rate was 31% (n = 13 of 42). At the maximum tolerated dose (MTD) of 400 mu g/d, the response rate was 70% (n = 7 of 10). Of these, five patients experienced MRD-negative complete responses, and 1 had a partial response, and 1 had a very good partial response; all 7 patients responded during the first cycle, and some responses lasted > 1 year. CONCLUSION In this study of AMG 420 in patients with relapsed/refractory multiple myeloma, the response rate was 70%, including 50% MRD-negative complete responses, at 400 mu g/d, the MTD for this study.
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页码:775 / +
页数:15
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