GLP-1 RA Treatment Patterns Among Type 2 Diabetes Patients in Five European Countries

Victoria Divino, Mitch DeKoven, Farhad Ali Khan, Kristina S Boye, Hélène Sapin, Kirsi Norrbacka, Victoria Divino, Mitch DeKoven, Farhad Ali Khan, Kristina S Boye, Hélène Sapin, Kirsi Norrbacka

Abstract

Introduction: Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are a relatively new class of injectable drugs used in the treatment of type 2 diabetes (T2D). This retrospective database study evaluated real-world treatment patterns of T2D patients initiating GLP-1 RAs in Belgium (BE), France (FR), Germany (DE), The Netherlands (NL) and Sweden (SE).

Methods: Adult T2D patients initiating exenatide twice daily (exBID), exenatide once weekly (exQW), liraglutide (LIRA) or lixisenatide (LIXI) during 2013 were identified using the QuintilesIMS (QuintilesIMS, Durham, NC, and Danbury, CT, USA) longitudinal retail pharmacy databases (LRx; BE/FR/DE/NL) and national health register data (SE). Therapy initiation date was termed 'index date.' Eligible patients had ≥180-day pre- and variable follow-up (minimum ≥360 days post-index). Baseline patient and treatment characteristics were assessed. Treatment modification and persistence were evaluated over the 1-year follow-up. Kaplan-Meier (KM) survival curves evaluated stopping of the index therapy (first of discontinuation or switch) over the available follow-up.

Results: A total of 4339 exBID, 1499 exQW, 20,955 LIRA and 1751 LIXI patients were included in the analysis (45.1-61.9% female; mean age range 57.1-62.9 years). Mean follow-up ranged from 17.7 to 30.7 months. Across countries/databases, the proportion experiencing a treatment modification at 1-year ranged from 84.1 to 93.8% for exBID, 53.3-73.4% for exQW and 59.5-80.5% for LIRA patients. The proportion of LIXI patients with treatment modification was 55.0% in Belgium (N = 20) and 96.9% in Germany (LIXI taken off the German market in April 2014). In KM analyses, LIRA patients had the lowest proportion stopping therapy, while exBID patients had the highest proportion stopping therapy, across databases, with the exception of LIXI patents.

Conclusion: Treatment patterns varied among GLP-1 RA patients, and persistence was generally highest among LIRA and lowest among exBID across countries. Longer term data would be useful, given the recent approval of several GLP-1 RA therapies.

Funding: Eli Lilly and Co., Indianapolis, IN, USA.

Keywords: Diabetes mellitus; Exenatide BID; Exenatide QW; Glucagon-like peptide 1/analogs and derivatives; Glucagon-like peptide 1/therapeutic use; Liraglutide; Lixisenatide; Persistence; Retrospective studies; Treatment patterns; Type 2/drug therapy.

Figures

Fig. 1
Fig. 1
Kaplan-Meier analyses for time to stop: a exBID; b LIRA; c exQW; d LIXI. BE Belgium, exBID exenatide twice daily, exQW exenatide once weekly, FR France; DE Germany, LIRA liraglutide, LIXI lixisenatide, NL The Netherlands, SE Sweden

References

    1. International Diabetes Federation. IDF Diabetes Atlas. 7th ed. Brussels: International Diabetes Federation; 2015. . Accessed May 10, 2016.
    1. Inzucchi SE, Bergenstal RM, Buse JB, et al. Management of hyperglycemia in type 2 diabetes, 2015: a patient-centered approach: update to a position statement of the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care. 2015;38:140–149. doi: 10.2337/dc14-2441.
    1. Lau DC, Teoh H. Impact of current and emerging glucose-lowering drugs on body weight in type 2 diabetes. Can J Diabetes. 2015;39(Suppl 5):S148–S154. doi: 10.1016/j.jcjd.2015.09.090.
    1. Owens DR. Clinical evidence for the earlier initiation of insulin therapy in type 2 diabetes. Diabetes Technol Ther. 2013;15:776–785. doi: 10.1089/dia.2013.0081.
    1. Byetta: EPAR–European Medicines Agency-Europa, European Medicines Agency. 2016. . Accessed Nov 4, 2016.
    1. Victoza: EPAR–European Medicines Agency-Europa, European Medicines Agency. 2016. . Accessed Nov 4, 2016.
    1. Bydureon: EPAR–European Medicines Agency-Europa, European Medicines Agency. 2016. . Accessed May 5, 2016.
    1. Lyxumia: EPAR–European Medicines Agency-Europa, European Medicines Agency. 2016. . Accessed May 5, 2016.
    1. Eperzan: EPAR–European Medicines Agency-Europa, European Medicines Agency. 2016. . Accessed Nov 4, 2016.
    1. Trulicity: EPAR–European Medicines Agency-Europa, European Medicines Agency. 2016. . Accessed May 5, 2016.
    1. Type 2 diabetes in adults: management (NG28): NICE clinical guidelines. 2015. . Accessed May 5, 2016.
    1. GLP-1-agonisten: MedicijnBalans. 2016. . Accessed Nov 4, 2016.
    1. Diabetes Mellitus Type 2: Domus Medica. 2015. . Accessed June 6, 2016.
    1. Fuchs S, Kostev L, Seitz L, Wohlleben M. Ermittlung der tatsächlichen Tagesdosierung von Liraglutid (PDD) unter realen Versorgungsbedingungen im Hinblick auf die Berechnung von Tagestherapiekosten. Diabetologie und Stoffwechsel. 2011;6:P234.
    1. Miller LA, Burudpakdee C, Zagar A, et al. Exenatide BID and liraglutide QD treatment patterns among type 2 diabetes patients in Germany. J Med Econ. 2012;15:746–757. doi: 10.3111/13696998.2012.679756.
    1. Divino V, DeKoven M, Hallinan S, et al. Glucagon-like Peptide-1 receptor agonist treatment patterns among type 2 diabetes patients in six European countries. Diabetes Ther. 2014;5:499–520. doi: 10.1007/s13300-014-0087-6.
    1. McDonell AL, Kiiskinen U, Zammit DC, et al. Estimating the real world daily usage and cost for exenatide twice daily and liraglutide in Germany, the Netherlands, and the UK based on volumes dispensed by pharmacies. Clinicoecon Outcomes Res. 2015;7:95–103. doi: 10.2147/CEOR.S69981.
    1. Johnston SS, Nguyen H, Felber E, et al. Retrospective study of adherence to glucagon-like peptide-1 receptor agonist therapy in patients with type 2 diabetes mellitus in the United States. Adv Ther. 2014;31:1119–1133. doi: 10.1007/s12325-014-0166-0.
    1. Pelletier EM, Pawaskar M, Smith PJ, Best JH, Chapman RH. Economic outcomes of exenatide vs liraglutide in type 2 diabetes patients in the United States: results from a retrospective claims database analysis. J Med Econ. 2012;15:1039–1050. doi: 10.3111/13696998.2012.688903.
    1. Yu M, Xie J, Fernandez Lando L, Kabul S, Swindle RW. Liraglutide versus exenatide once weekly: persistence, adherence, and early discontinuation. Clin Ther. 2016;38:149–160. doi: 10.1016/j.clinthera.2015.11.017.
    1. Saxenda: EPAR–European Medicines Agency-Europa, European Medicines Agency. 2016. . Accessed Nov 4, 2016.
    1. Sanofi Deutschland Fachpresse. Lyxumia® (Lixisenatid) in Deutschland außer Vertrieb. . Accessed July 18, 2016.
    1. Trujillo J, Nuffer W, Ellis S. GLP-1 receptor agonists: a review of head-to-head clinical studies. Ther Adv Endocrinol Metab. 2015;6:19–28. doi: 10.1177/2042018814559725.

Source: PubMed

3
Subskrybuj