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Original Article: Clinical

Real-world effectiveness of brentuximab vedotin versus physicians’ choice chemotherapy in patients with relapsed/refractory Hodgkin lymphoma following autologous stem cell transplantation in the United Kingdom and Germany

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Pages 1413-1419 | Received 18 Jul 2017, Accepted 18 Sep 2017, Published online: 18 Oct 2017
 

Abstract

This retrospective study compared effectiveness of (brentuximab vedotin) BV to other chemotherapies in patients with rrHL following an autologous stem cell transplant (ASCT). Data originated from a medical chart review of patients treated in real-world clinical settings at 50 sites in the United Kingdom and Germany. Inverse probability of treatment weights based on propensity scores were used to adjust for differences in baseline characteristics between treatment groups. Among 312 rrHL patients included, 196 received BV and 116 received physicians’ choice chemotherapy. Median PFS was significantly longer (27.0 months vs. 13.4 months; p = .0144) and 12-month OS survival greater (78.1% vs. 65.9%; p = .0129) with BV compared to chemotherapy. Documented adverse events included leukopenia (12.8%) and peripheral neuropathy (8.7%) for BV and leukopenia (12.1%), anemia (5.2%) and diarrhea (5.2%) for chemotherapy. In this real-world study, rrHL patients treated for relapse after ASCT with BV had longer median PFS and 12-month OS than patients receiving chemotherapy.

Acknowledgments

This study was sponsored by Takeda Pharmaceutical Company. The authors would like to acknowledge Melissa Hagan, PhD, MPH, Associate Medical Director, Health Economics and Outcomes Research, Ogilvy CommonHealth Worldwide; Caitlyn Solem, PhD, Senior Director of Health Economics and Outcomes Research, Pharmerit International; and Pete Wolthoff, Director of Research Operations, Medical Data Analytics, for their contributions to this study.

Potential conflict of interest

Disclosure forms provided by the authors are available with the full text of this article online at https://doi.org/10.1080/10428194.2017.1382698.

Additional information

Funding

This study was sponsored by Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited.