Long-term follow-up of hematologic relapse-free survival in a phase 2 study of blinatumomab in patients with MRD in B-lineage ALL

Author:

Topp Max S.12,Gökbuget Nicola3,Zugmaier Gerhard4,Degenhard Evelyn4,Goebeler Marie-Elisabeth12,Klinger Matthias4,Neumann Svenja A.5,Horst Heinz A.5,Raff Thorsten5,Viardot Andreas6,Stelljes Matthias7,Schaich Markus8,Köhne-Volland Rudolf9,Brüggemann Monika5,Ottmann Oliver G.3,Burmeister Thomas10,Baeuerle Patrick A.4,Nagorsen Dirk4,Schmidt Margit4,Einsele Hermann1,Riethmüller Gert11,Kneba Michael5,Hoelzer Dieter12,Kufer Peter4,Bargou Ralf C.12

Affiliation:

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

2. Comprehensive Cancer Center Mainfranken, University of Würzburg, Würzburg, Germany;

3. Center of Internal Medicine, Goethe University Frankfurt, Frankfurt, Germany;

4. Amgen Research (Munich) GmbH, Munich, Germany;

5. Medical Department II, University Hospital Schleswig-Holstein, Kiel, Germany;

6. Medical Department III, University Ulm, Ulm, Germany;

7. Medical Department A, University Münster, Münster, Germany;

8. Medical Department, Carl Gustav Carus University, Dresden, Germany;

9. Metronomia GmbH, Munich, Germany;

10. Department for Hematology and Oncology and Tumor Immunology, Charité - Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany;

11. Department of Immunology University Munich, Munich, Germany; and

12. Onkologikum, Frankfurt, Germany

Abstract

Abstract Persistence or recurrence of minimal residual disease (MRD) after chemotherapy results in clinical relapse in patients with acute lymphoblastic leukemia (ALL). In a phase 2 trial of B-lineage ALL patients with persistent or relapsed MRD, a T cell–engaging bispecific Ab construct induced an 80% MRD response rate. In the present study, we show that after a median follow-up of 33 months, the hematologic relapse-free survival of the entire evaluable study cohort of 20 patients was 61% (Kaplan-Meier estimate). The hema-tologic relapse-free survival rate of a subgroup of 9 patients who received allogeneic hematopoietic stem cell transplantation after blinatumomab treatment was 65% (Kaplan-Meier estimate). Of the subgroup of 6 Philadelphia chromosome–negative MRD responders with no further therapy after blinatumomab, 4 are in ongoing hematologic and molecular remission. We conclude that blinatumomab can induce long-lasting complete remission in B-lineage ALL patients with persistent or recurrent MRD. The original study and this follow-up study are registered at www.clinicaltrials.gov as NCT00198991 and NCT00198978, respectively.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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