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Original Articles

Blinatumomab versus chemotherapy in first salvage or in later salvage for B-cell precursor acute lymphoblastic leukemia

, , , , , , , & show all
Pages 2214-2222 | Received 08 Nov 2018, Accepted 24 Jan 2019, Published online: 05 Apr 2019
 

Abstract

Outcomes for adults with relapsed/refractory acute lymphoblastic leukemia (ALL) are poor with chemotherapy, particularly in later salvage. The TOWER study examined survival, remission, bridge to allogeneic hematopoietic stem cell transplantation (HSCT), and safety with blinatumomab versus chemotherapy. This report examined outcomes separately for study treatment as first or later salvage. Adults with Philadelphia chromosome-negative B-cell precursor ALL relapsed/refractory to chemotherapy were randomly assigned 2:1 to receive blinatumomab by continuous infusion for 4 weeks in 6-week cycles, or standard salvage chemotherapy. Overall survival for blinatumomab versus chemotherapy was higher both in first salvage and in later salvage. Safety was similar between patients in first salvage and those in later salvage. Blinatumomab as later salvage was associated with higher complete remission rates and served as a bridge to allogeneic HSCT, supporting the use of blinatumomab in both settings. This study is registered at www.clinicaltrials.gov as #NCT02013167.

Correction Statement

This article has been republished with minor changes. These changes do not impact the academic content of the article.

Acknowledgements

Jonathan Latham of PharmaScribe, LLC (on behalf of Amgen Inc.) assisted the authors with the preparation and submission of the manuscript. Robert Dawson of CACTUS (on behalf of Amgen Inc.) assisted the authors with preparation of the images.

Data deposition

Qualified researchers may request data from Amgen clinical studies. Complete details are available at http://www.amgen.com/datasharing.

Potential conflict of interest

Disclosure forms provided by the authors are available with the full text of this article online at http:\\doi:10.1080/10428194.2019.1576872

Additional information

Funding

This study was funded by Amgen Inc.