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

Max S. Topp(University of Würzburg), Nicola Gökbuget(Goethe University Frankfurt), Gerhard Zugmaier(Amgen (Germany)), Evelyn Degenhard(Amgen (Germany)), Marie-Elisabeth Goebeler(University of Würzburg), Matthias Klinger(Amgen (Germany)), Svenja Neumann(University Hospital Schleswig-Holstein), Heinz A. Horst(University Hospital Schleswig-Holstein), Thorsten Raff(University Hospital Schleswig-Holstein), Andreas Viardot(Universität Ulm), Matthias Stelljes, Markus Schaich(University Hospital Carl Gustav Carus), R Köhne-Volland, Monika Brüggemann(University Hospital Schleswig-Holstein), Oliver G. Ottmann(Goethe University Frankfurt), Thomas Burmeister(Charité - Universitätsmedizin Berlin), Patrick A. Baeuerle(Amgen (Germany)), Dirk Nagorsen(Amgen (Germany)), Margit Schmidt(Amgen (Germany)), Hermann Einsele(University of Würzburg), Gert Riethmüller, Michael Kneba(University Hospital Schleswig-Holstein), Dieter Hoelzer(Endokrinologikum), Peter Kufer(Amgen (Germany)), Ralf C. Bargou(University of Würzburg)
Blood
October 1, 2012
Cited by 468Open Access
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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.


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