Low leukemia burden improves blinatumomab efficacy in patients with relapsed/refractory B‐cell acute lymphoblastic leukemia

Author:

Queudeville Manon1,Stein Anthony S.2,Locatelli Franco3,Ebinger Martin1,Handgretinger Rupert1,Gökbuget Nicola4,Gore Lia5,Zeng Yi6ORCID,Gokani Priya7,Zugmaier Gerhard8,Kantarjian Hagop M.9

Affiliation:

1. Department of General Pediatrics, Hematology and Oncology Children's University Hospital Tübingen Tübingen Germany

2. Gehr Family Center for Leukemia Research City of Hope Duarte California USA

3. Department of Paediatric Haematology and Oncology IRCCS Ospedale Pediatrico Bambino Gesù Catholic University of the Sacred Heart Rome Italy

4. Department of Medicine University Hospital Goethe University Frankfurt Germany

5. Section of Pediatric Hematology/Oncology/Bone Marrow Transplant‐Cellular Therapeutics University of Colorado School of Medicine Aurora Colorado USA

6. Oncology TA Amgen Inc. Thousand Oaks California USA

7. International Biostatistics Amgen Ltd Cambridge UK

8. Amgen Research (Munich) GmbH Munich Germany

9. Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA

Abstract

AbstractBackgroundA lower baseline bone marrow blast percentage (bBMB%) is associated with better outcomes in patients with B‐cell acute lymphoblastic leukemia (B‐ALL) receiving blinatumomab. The objective of this analysis was to investigate the association between bBMB% and treatment outcomes in relapsed/refractory (R/R) B‐ALL.MethodsData from five trials of blinatumomab for R/R B‐ALL were pooled for analyses. Patients were placed in one of three groups: group 1, ≥50% bBMBs; group 2, ≥25% to <50% bBMBs; group 3, ≥5% to <25% bBMBs. Response and survival outcomes were compared between groups.ResultsData from 683 patients (166 pediatric, 517 adult) were analyzed. Collectively, patients in groups 2 and 3 had significantly higher odds of achieving a complete remission (CR) (odds ratio [OR], 3.50 [95% confidence interval (CI), 2.23–5.48] and 3.93 [95% CI, 2.50–6.18], respectively; p < .001) and minimal/measurable residual disease response (OR, 2.61 and 3.37, respectively; p < .001) when compared with group 1 (reference). Groups 2 and 3 had a 37% and 46% reduction in the risk of death (hazard ratio [HR], 0.63 and 0.54, respectively; p < .001) and a 41% and 43% reduction in the risk of an event (relapse or death) (HR, 0.59 and 0.57, respectively; p < .001) compared with group 1. No significant differences in response or survival outcomes were observed between groups 2 and 3. Seven of nine patients whose bBMB% was lowered to <50% with dexamethasone achieved CR with blinatumomab.ConclusionAny bBMB% <50% was associated with improved efficacy following blinatumomab treatment for R/R B‐ALL.

Publisher

Wiley

Subject

Cancer Research,Oncology

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