Type 2 & other diabetes

Patient stratification for determining optimal second-line and third-line therapy for type 2 diabetes: the TriMaster study

Nat MedPublished Randomised controlled trial

Authors' conclusion

In this precision medicine trial in type 2 diabetes, our findings support the use of simple, routinely available clinical measures to identify the drug class most likely to deliver the greatest glycemic reduction for a given patient.

Study context

Population
People with T2D on metformin alone or metformin plus SU, UKcrossover
Participants
525 people
Comparison
Sitagliptin vs canagliflozin vs pioglitazone, 16 weeks each, added to metformin ± SU
Primary endpoint
Achieved HbA1c difference between strata for the two drugs (for both hypotheses)
Follow-up
16 weeks of treatment with each drug
Methodological detailsdouble-blind, three-way crossover, UK-based
  • Double-blind
  • Three-way crossover
  • UK-based

Primary result

As reported in the abstract

Achieved HbA1c difference between strata for the two drugs
Estimate (95% CI)P value
Pioglitazonevs Sitagliptinlower HbA1c on pioglitazone than sitagliptin in BMI >30; n = 356
difference in achieved HbA1c, BMI >30 vs ≤30 kg/m² 2.88 mmol/mol(0.98–4.79)
P = 0.003
Sitagliptinvs Canagliflozinlower HbA1c on sitagliptin than canagliflozin in eGFR 60-90; n = 342
difference in achieved HbA1c, eGFR 60-90 vs >90 ml/min/1.73 m² 2.90 mmol/mol(1.19–4.61)
P = 0.001

Further findings

Achieved HbA1c overall — between Pioglitazone and Sitagliptin · three drugs compared; similar

P = 0.2

Achieved HbA1c overall

Achieved HbA1c similar for the three drugs

Safety

Adverse events reported
2,201
Randomized participants with an adverse event on at least one study drug
447/525 (85%)

Original publication

Patient stratification for determining optimal second-line and third-line therapy for type 2 diabetes: the TriMaster study. Nat Med. Published 7 December 2022. doi:10.1038/s41591-022-02120-7

Composed by AI from the published abstract and checked against it. How Briefs are made →

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