International Trial of the Edmonton Protocol for Islet Transplantation

A. M. James Shapiro(University of Alberta), Camillo Ricordi(University of Miami), Bernhard J. Hering(University of Minnesota System), Hugh Auchincloss(Harvard University), Robert Lindblad(Emmes (United States)), R. Paul Robertson(University of Washington), Antonio Secchi(San Raffaele University of Rome), Mathias D. Brendel(Justus-Liebig-Universität Gießen), Thierry Berney(University of Geneva), Daniel C. Brennan(Washington University in St. Louis), Enrico Cagliero(Harvard University), Rodolfo Alejandro(University of Miami), Edmond A. Ryan(University of Alberta), Barbara DiMercurio(National Institute of Allergy and Infectious Diseases), Philippe Morel(University of Geneva), Kenneth S. Polonsky(Washington University in St. Louis), Jo-Anna Reems(University of Washington), Reinhard G. Bretzel(Justus-Liebig-Universität Gießen), Federico Bertuzzi(San Raffaele University of Rome), Tatiana Froud(University of Miami), Raja Kandaswamy(University of Minnesota System), David E.R. Sutherland(University of Minnesota System), George S. Eisenbarth(University of Colorado Boulder), Miriam Segal(University of Minnesota System), Jutta Preiksaitis(University of Alberta), Gregory S. Korbutt(University of Alberta), Franca B. Barton(Emmes (United States)), Lisa Viviano(National Institute of Allergy and Infectious Diseases), Vicki Seyfert‐Margolis(Immune Tolerance Network), Jeffrey A. Bluestone(Immune Tolerance Network), Jonathan R. T. Lakey(University of Alberta)
New England Journal of Medicine
September 27, 2006
Cited by 1,939Open Access
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Abstract

BACKGROUND: Islet transplantation offers the potential to improve glycemic control in a subgroup of patients with type 1 diabetes mellitus who are disabled by refractory hypoglycemia. We conducted an international, multicenter trial to explore the feasibility and reproducibility of islet transplantation with the use of a single common protocol (the Edmonton protocol). METHODS: We enrolled 36 subjects with type 1 diabetes mellitus, who underwent islet transplantation at nine international sites. Islets were prepared from pancreases of deceased donors and were transplanted within 2 hours after purification, without culture. The primary end point was defined as insulin independence with adequate glycemic control 1 year after the final transplantation. RESULTS: Of the 36 subjects, 16 (44%) met the primary end point, 10 (28%) had partial function, and 10 (28%) had complete graft loss 1 year after the final transplantation. A total of 21 subjects (58%) attained insulin independence with good glycemic control at any point throughout the trial. Of these subjects, 16 (76%) required insulin again at 2 years; 5 of the 16 subjects who reached the primary end point (31%) remained insulin-independent at 2 years. CONCLUSIONS: Islet transplantation with the use of the Edmonton protocol can successfully restore long-term endogenous insulin production and glycemic stability in subjects with type 1 diabetes mellitus and unstable control, but insulin independence is usually not sustainable. Persistent islet function even without insulin independence provides both protection from severe hypoglycemia and improved levels of glycated hemoglobin. (ClinicalTrials.gov number, NCT00014911 [ClinicalTrials.gov].).


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