Juliane Beck1, Andreas Schwarzer2, Dietrich Gläser3, Lars-Olof Mügge4, Jens Uhlig5, Simone Heyn1, Brigitte Kragl6, Martin Mohren7, Franz Albert Hoffmann8, Thoralf Lange9, Thomas Schliwa1, Thomas Zehrfeld10, Cornelia Becker8, Ute Kreibich11, Cornelia Winkelmann12, Thomas Edelmann13, Marc Andrea1, Marius Bill1, Madlen Jentzsch1, Sebastian Schwind1, Dietger Niederwieser1, Wolfram Pönisch14. 1. Department of Haematology and Oncology, University of Leipzig, Johannisallee 32A, 04103, Leipzig, Germany. 2. Haematology Practice, Strümpelstrasse 41, Leipzig, Germany. 3. Department of Haematology and Oncology, Klinikum Südstadt Rostock, Rostock, Germany. 4. Department of Haematology and Oncology, University of Jena, Jena, Germany. 5. Haematology Practice, Schulstrasse 1, Naunhof, Germany. 6. Department of Haematology and Oncology, University of Rostock, Rostock, Germany. 7. Department of Haematology and Oncology, Johanniter Krankenhaus, Stendal, Germany. 8. Haematology Practice, Biedermannstrasse 84, Leipzig, Germany. 9. Department of Haematology and Oncology, Asklepios Hospital, Weissenfels, Germany. 10. Department of Haematology and Oncology, Hospital Johann Kentmann, Torgau, Germany. 11. Department of Haematology and Oncology, Heinrich-Braun-Hospital, Zwickau, Germany. 12. Department of Haematology and Oncology, Paul Gerhardt Stift, Wittenberg, Germany. 13. Haematology Practice, Theodor-Heuss-Str. 2, Schkeuditz, Germany. 14. Department of Haematology and Oncology, University of Leipzig, Johannisallee 32A, 04103, Leipzig, Germany. Wolfram.Poenisch@medizin.uni-leipzig.de.
Abstract
INTRODUCTION: While lenalidomide monotherapy is established for relapsed and/or refractory multiple myeloma (MM) treatment, combination therapies including lenalidomide are still under investigation in a number of phase 2/3 studies. In the current study, a treatment regime of lenalidomide (Revlimid®), bendamustine and prednisolone (RBP) was tested in patients with relapsed/refractory MM. METHODS: In the previously completed phase 1 study RBP with a dose of 75 mg/m2 bendamustine days 1-2, prednisolone 100 mg days 1-4 and 25 mg lenalidomide days 1-21 was well tolerated. RESULTS: Between July 2011 and September 2013, 25 patients were included in this analysis. The median number of previous treatments was 1 (range 1-2). Twenty-two patients (88%) responded after at least two cycles of RBP (one sCR, five nCR, eight VGPR and eight PR). The median time to first haematological response was 28 days, and median time to best response was 56 days. Due to increased haematological toxicity a dose reduction in most patients required in subsequent cycles of therapy. The median progression-free and overall survival was 22 and 38 months, respectively. In conclusion RBP is a highly effective therapy for patients with relapsed/refractory MM. In contrast to our phase 1 study, dose reduction was necessary in many patients because of haematological toxicity.
INTRODUCTION: While lenalidomide monotherapy is established for relapsed and/or refractory multiple myeloma (MM) treatment, combination therapies including lenalidomide are still under investigation in a number of phase 2/3 studies. In the current study, a treatment regime of lenalidomide (Revlimid®), bendamustine and prednisolone (RBP) was tested in patients with relapsed/refractory MM. METHODS: In the previously completed phase 1 study RBP with a dose of 75 mg/m2 bendamustine days 1-2, prednisolone 100 mg days 1-4 and 25 mg lenalidomide days 1-21 was well tolerated. RESULTS: Between July 2011 and September 2013, 25 patients were included in this analysis. The median number of previous treatments was 1 (range 1-2). Twenty-two patients (88%) responded after at least two cycles of RBP (one sCR, five nCR, eight VGPR and eight PR). The median time to first haematological response was 28 days, and median time to best response was 56 days. Due to increased haematological toxicity a dose reduction in most patients required in subsequent cycles of therapy. The median progression-free and overall survival was 22 and 38 months, respectively. In conclusion RBP is a highly effective therapy for patients with relapsed/refractory MM. In contrast to our phase 1 study, dose reduction was necessary in many patients because of haematological toxicity.
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