Real-world outcomes of treatment with insulin glargine 300 U/mL versus standard-of-care in people with uncontrolled type 2 diabetes mellitus

dc.contributor.authorFreemantle, Nick
dc.contributor.authorMauricio Puente, Dídac
dc.contributor.authorGiaccari, Andrea
dc.contributor.authorBailey, Timothy
dc.contributor.authorRoussel, Ronan
dc.contributor.authorFranco, Denise
dc.contributor.authorBerthou, Baptiste
dc.contributor.authorPilorget, Valerie
dc.contributor.authorWesterbacka, Jukka
dc.contributor.authorBosnyak, Zsolt
dc.contributor.authorBonnemaire, Mireille
dc.contributor.authorCali, Anna M. G.
dc.contributor.authorNguyên-Pascal, My-Liên
dc.contributor.authorPenfornis, Alfred
dc.contributor.authorPérez Maraver, Manuel
dc.contributor.authorSeufert, Jochen
dc.contributor.authorSullivan, Sean D.
dc.contributor.authorWilding, John
dc.contributor.authorWysham, Carol
dc.contributor.authorDavies, Melanie
dc.date.accessioned2021-01-20T17:32:35Z
dc.date.available2021-01-20T17:32:35Z
dc.date.issued2020-04-02
dc.date.updated2020-12-21T13:16:50Z
dc.description.abstractObjective: To compare real-world outcomes with newer (insulin glargine 300 U/mL; Gla-300) versus standard of care (SoC) basal insulins (BIs) in the REACH (insulin-naive; NCT02967224) and REGAIN (basal insulin-treated; NCT02967211) studies in participants with uncontrolled type 2 diabetes (T2DM) in Europe and Brazil. Methods: In these open-label, parallel-group, pragmatic studies, patients (HbA(1c) > 7.0%) were randomized to Gla-300 or SoC BI for a 6-month treatment period (to demonstrate non-inferiority of Gla-300 vs SoC BIs for HbA(1c) change [non-inferiority margin 0.3%]) and a 6-month extension period (continuing with their assigned treatment). Insulin titration/other medication changes were at investigator/patient discretion post-randomization. Results: Overall, 703 patients were randomized to treatment in REACH (Gla-300, n = 352; SoC, n = 351) and 609 (Gla-300, n = 305, SoC, n = 304) in REGAIN. The primary outcome, non-inferiority of Gla-300 versus SoC for HbA(1c) change from baseline to month 6, was met in REACH (least squares [LS] mean difference 0.12% [95% CI -0.046 to 0.281]) but not REGAIN (LS mean difference 0.17% [0.015-0.329]); no between-treatment difference in HbA(1c) change was shown after 12 months in either study. BI dose increased minimally from baseline to 12 months in REACH (Gla-300, +0.17 U/kg; SoC, +0.15 U/kg) and REGAIN (Gla-300, +0.11 U/kg; SoC, +0.07 U/kg). Hypoglycemia incidence was low and similar between treatment arms in both studies. Conclusions: In both REACH and REGAIN, no differences in glycemic control or hypoglycemia outcomes with Gla-300 versus SoC BIs were seen over 12 months. However, the suboptimal insulin titration in REACH and REGAIN limits comparisons of outcomes between treatment arms and suggests that more titration instruction/support may be required for patients to fully derive the benefits from newer basal insulin formulations.
dc.format.extent10 p.
dc.format.mimetypeapplication/pdf
dc.identifier.pmid31865758
dc.identifier.urihttps://hdl.handle.net/2445/173260
dc.language.isoeng
dc.publisherTaylor & Francis Ltd.
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1080/03007995.2019.1708287
dc.relation.ispartofCurrent Medical Research and Opinion, 2020, vol. 36, num. 4, p. 571-581
dc.relation.urihttps://doi.org/10.1080/03007995.2019.1708287
dc.rightscc by-nc-nd (c) Freemantle et al., 2020
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationDiabetis
dc.subject.classificationInsulina
dc.subject.otherDiabetes
dc.subject.otherInsulin
dc.titleReal-world outcomes of treatment with insulin glargine 300 U/mL versus standard-of-care in people with uncontrolled type 2 diabetes mellitus
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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