Real-World Use of Oral Semaglutide in Adults with Type 2 Diabetes in the PIONEER REAL Netherlands Multicentre, Prospective, Observational Study

被引:14
作者
van Houtum, William [1 ]
Schrombges, Patrick [2 ]
Amadid, Hanan [3 ]
van Bon, Arianne C. [4 ]
Braae, Uffe C. [3 ]
Hoogstraten, Charlotte [5 ]
Herrings, Hans [6 ]
机构
[1] Spaarne Gasthuis, Dept Internal Med, Spaarnepoort 1, NL-2134 TM Hoofddorp, Netherlands
[2] Tunnis Huisartsen, Sint Anthonis, Netherlands
[3] Novo Nordisk AS, Soborg, Denmark
[4] Rijnstate, Dept Internal Med, Arnhem, Netherlands
[5] Novo Nordisk AS, Alphen Aan Den Rijn, Netherlands
[6] Med Ctr Den Bosch Oost, sHertogenbosch, Netherlands
关键词
Body weight; GLP-1 receptor agonist; Glycaemic control; HbA1c; Incretin therapy; Real-world evidence; Semaglutide; Type; 2; diabetes;
D O I
10.1007/s13300-024-01588-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: In this phase 4, multicentre, prospective, non-interventional PIONEER REAL Netherlands study, we assessed clinical outcomes associated with once-daily oral semaglutide use in real-world clinical practice in adults living with type 2 diabetes (T2D) na & iuml;ve to injectable glucose-lowering medication. Methods: Participants initiated on oral semaglutide were followed for 34-44 weeks. Change in glycated haemoglobin (HbA1c) from baseline (BL) to end of study (EOS) was the primary endpoint; secondary endpoints included change in body weight (BW) from BL to EOS, the proportion of participants with HbA1c < 7.0% at EOS and the composite endpoints of HbA1c reduction >= 1.0%-points with BW reduction >= 3% or >= 5% at EOS. Treatment satisfaction was assessed using the Diabetes Treatment Satisfaction Questionnaire (DTSQ status/change). Safety was evaluated in all participants who initiated oral semaglutide treatment. Results: Oral semaglutide was initiated in 187 participants; 94.1% completed the study and 78.6% remained on treatment at EOS. At BL, 54.0% of participants were male, mean age was 58.8 years, mean duration of T2D was 8.7 years and mean body mass index was 35.1 kg/m(2); mean HbA1c was 8.6% and mean BW was 103.1 kg. Significant improvements from BL to EOS were observed for HbA1c and BW (estimated change [95% confidence interval]: - 1.16%-points [- 1.48 to - 0.85]; p < 0.0001, and - 5.84 kg [- 6.88 to - 4.80]; p < 0.0001, respectively). At EOS, 47.5% of participants had an HbA1c level < 7.0%; 41.8% and 35.5% of participants achieved composite endpoints of HbA1c reduction >= 1.0%-points plus BW reduction >= 3% or >= 5%, respectively. DTSQ status and change scores improved by 2.1 (p = 0.0003) and 10.8 points (p < 0.0001), respectively. Oral semaglutide was easy or very easy to consume for 81.5% of participants. Adverse events were mostly mild/moderate, with gastrointestinal disorders being the most common. Conclusion: In this real-world population, we reported clinically significant reductions in HbA1c and BW, improved treatment satisfaction and no new safety concerns.
引用
收藏
页码:1749 / 1768
页数:20
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