Diabetologie und Stoffwechsel 2021; 16(S 01): S4-S5
DOI: 10.1055/s-0041-1727304
01. Klinische Diabetologie

The Real-World Observational Prospective Study of Health Outcomes with Dulaglutide and Liraglutide in Type 2 Diabetes Patients (TROPHIES): Design and Baseline Characteristics

LE Garcia-Pérez
1   Lilly, S.A., Medical, Alcobendas, Spain
,
H Sapin
2   Lilly France SAS, Medical, Neuilly Sur Seine, France
,
K Norrbacka
3   Eli Lilly and Company, Medical, Helsinki, Finland
,
B Guerci
4   Hôpital Brabois Adultes, Medical, CHRU de Nancy, France
,
F Giorgino
5   University of Bari, Medical, Aldo Moro, Italy
,
U Aigner
6   Versdias GmbH, Medical, Sulzbach-Rosenberg, Germany
,
MO Federici
7   Eli Lilly Company Italia SpA, Medical, Florence, Italy
,
R Gentilella
8   Former employee of Eli Lilly Company Italia SpA, Medical, Florence, Italy
,
E Heitmann
9   Lilly Deutschland GmbH, Medical, Bad Homburg, Germany
,
H Jung
9   Lilly Deutschland GmbH, Medical, Bad Homburg, Germany
,
M Rosilio
2   Lilly France SAS, Medical, Neuilly Sur Seine, France
,
K Boye
10   Eli Lilly and Company, Medical, Indianapolis, United States
› Author Affiliations
 
 

    Objective Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are usually recommended as first injectable therapy for type 2 diabetes (T2D). Randomized clinical trials are standard for assessing efficacy and safety, observational studies are valuable to understand GLP-1RA use in clinical practice. Methods: TROPHIES is a 24-month, prospective, observational study in France, Germany, Italy in adult patients with T2 D initiating first injectable glucose-loweringtreatment with once-weekly dulaglutide / once-daily liraglutide. The primary outcome, time on first GLP-1RA without significant treatment change due to T2D-related factors, was defined as discontinuation of this GLP-1RA/intensification of glucose-lowering treatment. At baseline, demographics, T2 D duration, HbA1c levels, reported HbA1c targets, pre-existing diabetes-related diagnoses and concomitantly used oral glucose-lowering medications were assessed. Results: To date, data from 2065 patients initiating dulaglutide (1089) or liraglutide (976) are analyzed. For patients initiating dulaglutide or liraglutide, mean age 58.9 and 59.4yr, 55.3 % and 57.4 % were male, with mean duration of T2 D 8.7 and 8.3yr, and mean BMI 33.8 and 34.1kg/m2, respectively. Mean baseline HbA1c level 8.2 % (dulaglutide) and 8.3 % (liraglutide) exceeded reported mean HbA1c target 6.9 %. Macrovascular and microvascular diabetes related conditions were reported in 8.2 % and 17.7 % (dulaglutide) and 11.5 % and 15.5 % (liraglutide) patients, respectively. Of patients initiating dulaglutide or liraglutide, 27.5 % and 25.5 % had taken ≥2 concomitant oral glucose-lowering medications, respectively, biguanides being most common. Conclusion: In both groups, BMI reflected obesity. HbA1c levels exceeded reported targets justifying treatment intensification with GLP-1RA after ~8.5yr of diabetes. This study helps understand profiles of patients being prescribed dulaglutide or liraglutide in France, Germany, Italy.


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    Interessenskonflikt

    1. Angestellte der Lilly Deutschland GmbH

    3. Besitz von Firmenaktien

    6. Sponsor: Eli Lilly & Company

    Publication History

    Article published online:
    06 May 2021

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