1. Comparative Efficacy and Safety of Ultra-Long-Acting, Long-Acting, Intermediate-Acting, and Biosimilar Insulins for Type 1 Diabetes Mellitus: a Systematic Review and Network Meta-Analysis
- Author
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Andrea C. Tricco, Sharon E. Straus, Huda M. Ashoor, Myanca Rodrigues, Lorenzo Moja, Nazia Darvesh, Ba' Pham, Jesmin Antony, Fatemeh Yazdi, Paul A. Khan, Zachary Bouck, Marco Ghassemi, John D. Ivory, Catherine H. Yu, Vera Nincic, and Areti Angeliki Veroniki
- Subjects
medicine.medical_specialty ,medicine.medical_treatment ,Network Meta-Analysis ,01 natural sciences ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,Randomized controlled trial ,law ,Internal medicine ,Diabetes mellitus ,Internal Medicine ,Humans ,Hypoglycemic Agents ,Insulin ,Medicine ,030212 general & internal medicine ,0101 mathematics ,Biosimilar Pharmaceuticals ,Glycated Hemoglobin ,Review Paper ,Type 1 diabetes ,business.industry ,010102 general mathematics ,Weight change ,Biosimilar ,Odds ratio ,medicine.disease ,Insulin, Long-Acting ,Diabetes Mellitus, Type 1 ,Meta-analysis ,business - Abstract
BACKGROUND: Increasing availability of competing biosimilar alternatives makes it challenging to make treatment decisions. The purpose of this review is to evaluate the comparative efficacy and safety of ultra-long-/long-/intermediate-acting insulin products and biosimilar insulin compared to human/animal insulin in adults with type 1 diabetes mellitus (T1DM). METHODS: MEDLINE, EMBASE, CENTRAL, and grey literature were searched from inception to March 27, 2019. Randomized controlled trials (RCTs), quasi-experimental studies, and cohort studies of adults with T1DM receiving ultra-long-/long-/intermediate-acting insulin, compared to each other, as well as biosimilar insulin compared to human/animal insulin were eligible for inclusion. Two reviewers independently screened studies, abstracted data, and appraised risk-of-bias. Pairwise meta-analyses and network meta-analyses (NMA) were conducted. Summary effect measures were mean differences (MD) and odds ratios (OR). RESULTS: We included 65 unique studies examining 14,200 patients with T1DM. Both ultra-long-acting and long-acting insulin were superior to intermediate-acting insulin in reducing A1c, FPG, weight gain, and the incidence of major, serious, or nocturnal hypoglycemia. For fasting blood glucose, long-acting once a day (od) was superior to long-acting twice a day (bid) (MD - 0.44, 95% CI: - 0.81 to - 0.06) and ultra-long-acting od was superior to long-acting bid (MD - 0.73, 95% CI - 1.36 to - 0.11). For weight change, long-acting od was inferior to long-acting bid (MD 0.58, 95% CI: 0.05 to 1.10) and long-acting bid was superior to long-action biosimilar od (MD - 0.90, 95% CI: - 1.67 to - 0.12). CONCLUSIONS: Our results can be used to tailor insulin treatment according to the desired results of patients and clinicians and inform strategies to establish a competitive clinical market, address systemic barriers, expand the pool of potential suppliers, and favor insulin price reduction. PROSPERO REGISTRATION: CRD42017077051 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11606-021-06642-7.
- Published
- 2021