Patient preferences and quality of life implications of ravulizumab (every 8 weeks) and eculizumab (every 2 weeks) for the treatment of paroxysmal nocturnal hemoglobinuria

PLoS One. 2020 Sep 4;15(9):e0237497. doi: 10.1371/journal.pone.0237497. eCollection 2020.

Abstract

Background: Eculizumab has transformed management of paroxysmal nocturnal hemoglobinuria (PNH) since its approval. However, its biweekly dosing regimen remains a high treatment burden. Ravulizumab administered every 8 weeks demonstrated noninferiority to eculizumab in two phase 3 trials. In regions where two PNH treatment options are available, it is important to consider patient preference.

Objective: The aim of this study was to assess patient preference for ravulizumab or eculizumab.

Methods: Study 302s (ALXN1210-PNH-302s) enrolled PNH patients who participated in the extension period of phase 3 study ALXN1210-PNH-302. In the parent study, eculizumab-experienced adult PNH patients received ravulizumab or eculizumab during a 26-week primary evaluation period. All patients in the extension period received ravulizumab. In study 302s, patient treatment preference was evaluated using an 11-item PNH-specific Patient Preference Questionnaire (PNH-PPQ©). Of 98 patients, 95 completed PNH-PPQ© per protocol for analysis.

Results: Overall, 93% of patients preferred ravulizumab whereas 7% of patients either had no preference (6%) or preferred eculizumab (1%) (P < 0.001). For specific aspects of treatment, ravulizumab was preferred (in comparison to no preference or eculizumab) on infusion frequency (98% vs. 0% vs. 2%), ability to plan activities (98% vs. 0% vs. 2%), and overall quality of life (88% vs. 11% vs. 1%), among other aspects. Most participants selected frequency of infusions as the most important factor determining preference (43%), followed by overall quality of life (23%).

Conclusion: This study shows that a substantial proportion of patients preferred ravulizumab over eculizumab and provides an important patient perspective on PNH treatment when there is more than one treatment option.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • Complement Inactivating Agents / therapeutic use*
  • Female
  • Hemoglobinuria, Paroxysmal / drug therapy*
  • Humans
  • Middle Aged
  • Patient Preference
  • Quality of Life
  • Young Adult

Substances

  • Antibodies, Monoclonal, Humanized
  • Complement Inactivating Agents
  • eculizumab
  • ravulizumab

Grants and funding

This study was funded by Alexion Pharmaceuticals, Inc. (Boston, MA, USA). Alexion Pharmaceuticals, Inc., provided support in the form of salaries and stocks to authors (Ioannis Tomazos and Masayo Ogawa) and contributors (Ji Yu, Ke Zu, Scott Rottinghaus, and Simu Thomas) of this study. The specific roles of the authors are articulated in the author contributions section, and the contributors are acknowledged in the Acknowledgments. The sponsor (Alexion Pharmaceuticals, Inc.) had no additional role and was not involved in interpretation of the data, reporting of the results, or preparation of the manuscript. The decision to submit the manuscript to PLoS One was made independently by the authors with no influence from the sponsor. Medical writing and editorial support were provided by ApotheCom (Yardley, PA, USA) and funded by Alexion Pharmaceuticals, Inc. (Boston, MA, USA).