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

Author:

Topp Max S.1,Duell Johannes1,Zugmaier Gerhard2,Attal Michel3,Moreau Philippe4,Langer Christian5,Krönke Jan6,Facon Thierry7,Salnikov Alexey V.8,Lesley Robin9,Beutner Karl10,Kalabus James9,Rasmussen Erik10,Riemann Kathrin8,Minella Alex C.10,Munzert Gerd8,Einsele Hermann1

Affiliation:

1. Department of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany

2. Amgen Research (Munich), Munich, Germany

3. University of Toulouse, Toulouse, France

4. Hematology Department, University Hospital Center of Nantes, Nantes, France

5. Kempten Clinic, Kempten, Germany

6. Ulm University, Ulm, Germany

7. Regional University Hospital of Lille, Lille, France

8. Boehringer Ingelheim, Biberach, Germany

9. Amgen, South San Francisco, CA

10. Amgen, Thousand Oaks, CA

Abstract

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/104 bone marrow cells by flow cytometry. RESULTS Forty-two patients received AMG 420 at 0.2-800 μg/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 μg/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 μg/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 μg/d, the MTD for this study.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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