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The Real-World Observational Prospective Study of Health Outcomes with Dulaglutide and Liraglutide in Patients with Type 2 Diabetes (TROPHIES): Patient disposition, clinical characteristics and treatment persistence at 12 months.
Guerci, Bruno; Giorgino, Francesco; Sapin, Hélène; Boye, Kristina; Lebrec, Jérémie; Federici, Marco Orsini; Heitmann, Elke; Dib, Anne; Füchtenbusch, Martin; García-Pérez, Luis-Emilio.
Afiliação
  • Guerci B; Department of Endocrinology, Diabetology and Nutrition, University Hospital of Nancy, Vandoeuvre-lès-Nancy, France.
  • Giorgino F; Department of Emergency and Organ Transplantation, Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro, Bari, Italy.
  • Sapin H; Statistics and Real World Analytics, Lilly France SAS, Neuilly-sur-Seine, France.
  • Boye K; Value, Evidence, and Outcomes, Eli Lilly and Company, Indianapolis, Indiana, USA.
  • Lebrec J; Real World Access and Analytics, HaaPACS GmbH, Schriesheim, Germany.
  • Federici MO; Medical Affairs, Eli Lilly Italia SpA, Sesto Fiorentino, Italy.
  • Heitmann E; Medical Affairs, Lilly Deutschland GmbH, Bad Homburg, Germany.
  • Dib A; Medical Affairs, Lilly France SAS, Neuilly-sur-Seine, France.
  • Füchtenbusch M; Diabetes Research Institute, Munich, Germany.
  • García-Pérez LE; Diabetes Global Medical Affairs, Lilly, S.A., Alcobendas, Spain.
Diabetes Obes Metab ; 24(12): 2373-2382, 2022 12.
Article em En | MEDLINE | ID: mdl-35876235
ABSTRACT

AIMS:

The primary objective of the TROPHIES observational study is to estimate the duration of treatment on dulaglutide or liraglutide without a significant treatment change by 24 months in patients with type 2 diabetes (T2D) initiating their first injectable treatment with these glucagon-like peptide-1 receptor agonists (GLP-1 RAs). This manuscript presents 12-month interim data. MATERIALS AND

METHODS:

TROPHIES is a prospective, non-comparative, observational study of patients with T2D in Europe, naïve to injectable antihyperglycaemic treatments and initiating dulaglutide or liraglutide. Data on clinical characteristics, GLP-1 RA persistence and treatment patterns of glucose-lowering medication were collected at initiation of first injectable therapy and by 12 months.

RESULTS:

By 12 months, 1014 dulaglutide and 991 liraglutide patients were eligible across France, Germany and Italy. Both cohorts presented a high probability [95% confidence interval (CI)] of GLP-1 RA persistence [dulaglutide, 0.88 (0.86 to 0.90); liraglutide, 0.83 (0.80 to 0.85)] and reduction in mean glycated haemoglobin percentage (95% CI) from baseline [dulaglutide, -1.18 (-1.27 to -1.08); liraglutide, -1.15 (-1.26 to -1.05)] with 48.2% of dulaglutide and 41.2% of liraglutide patients reaching their individualized glycated haemoglobin percentage target set by the physician at baseline. Mean weight (95% CI) change from baseline was -3.2 kg (-3.6 to -2.8) for dulaglutide and -3.4 kg (-3.9 to -3.0) for liraglutide. Slight changes in concomitant medications were observed compared with baseline.

CONCLUSIONS:

In the real-world setting, dulaglutide and liraglutide cohorts achieved good persistence with similarly improved glycaemic control that was accompanied by weight loss at 12 months, consistent with previous clinical trial results.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Liraglutida Tipo de estudo: Clinical_trials / Observational_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Liraglutida Tipo de estudo: Clinical_trials / Observational_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article