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Low-Dose ATG/GCSF in Established Type 1 Diabetes: A Five-Year Follow-up Report.

Authors :
Lin, Andrea
Lin, Andrea
Mack, Jasmine A
Bruggeman, Brittany
Jacobsen, Laura M
Posgai, Amanda L
Wasserfall, Clive H
Brusko, Todd M
Atkinson, Mark A
Gitelman, Stephen E
Gottlieb, Peter A
Gurka, Matthew J
Mathews, Clayton E
Schatz, Desmond A
Haller, Michael J
Lin, Andrea
Lin, Andrea
Mack, Jasmine A
Bruggeman, Brittany
Jacobsen, Laura M
Posgai, Amanda L
Wasserfall, Clive H
Brusko, Todd M
Atkinson, Mark A
Gitelman, Stephen E
Gottlieb, Peter A
Gurka, Matthew J
Mathews, Clayton E
Schatz, Desmond A
Haller, Michael J
Source :
Diabetes; vol 70, iss 5, 1123-1129; 0012-1797
Publication Year :
2021

Abstract

Previously, we demonstrated low-dose antithymocyte globulin (ATG) and granulocyte colony-stimulating factor (GCSF) immunotherapy preserved C-peptide for 2 years in a pilot study of patients with established type 1 diabetes (n = 25). Here, we evaluated the long-term outcomes of ATG/GCSF in study participants with 5 years of available follow-up data (n = 15). The primary end point was area under the curve (AUC) C-peptide during a 2-h mixed-meal tolerance test. After 5 years, there were no statistically significant differences in AUC C-peptide when comparing those who received ATG/GCSF versus placebo (P = 0.41). A modeling framework based on mean trajectories in C-peptide AUC over 5 years, accounting for differing trends between groups, was applied to recategorize responders (n = 9) and nonresponders (n = 7). ATG/GCSF reponders demonstrated nearly unchanged HbA1c over 5 years (mean [95% CI] adjusted change 0.29% [-0.69%, 1.27%]), but the study was not powered for comparisons against nonresponders 1.75% (-0.57%, 4.06%) or placebo recipients 1.44% (0.21%, 2.66%). These data underscore the importance of long-term follow-up in previous and ongoing phase 2 trials of low-dose ATG in recent-onset type 1 diabetes.

Details

Database :
OAIster
Journal :
Diabetes; vol 70, iss 5, 1123-1129; 0012-1797
Notes :
application/pdf, Diabetes vol 70, iss 5, 1123-1129 0012-1797
Publication Type :
Electronic Resource
Accession number :
edsoai.on1391595821
Document Type :
Electronic Resource