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Islet Allotransplantation With Steroid Free Immunosuppression

23. april 2012 opdateret af: University Hospital, Lille

Sequential Islet Transplantation With Steroid Free Immunosuppression for Type 1 Diabetes

The restoration of endogenous insulin secretion carries significant hopes for shifting the paradigm of life long exogenous insulin therapy in selected groups of patients with type 1 diabetes(T1D). After decades of frustrating clinical attempts, the Edmonton group set up in 2000 new standards for islet transplantation in patients with brittle T1D by achieving insulin independence in 80 percent of patients. These seminal results have however proved much more difficult to duplicate than initially expected.

This single center phase 2 clinical trial, duplicating the Edmonton protocol, is designed for confirming the consistent short term efficacy and safety of sequential islet allotransplantation with steroid free immunosuppression in patients with severe T1D.

Studieoversigt

Detaljeret beskrivelse

The short term effectiveness of islet transplantation for alleviating hypoglycemia and controlling glucose homeostasis while limiting or even avoiding the nedd for exogenous insulin has been established despite protocol modifications in donor selection, islet preparation or recipient treatment, insulin independence with adequate metabolic control was however rarely prolonged beyond two years. The most frequently proposed explanations include chronic allogenic rejection, recurrence of autoimmunity and beta cell toxicity from administered immunosuppressive drugs.

Fourteen patients were enrolled in this single center phase 2 trial initiated in 2003. Eligible patients were males or females between 18 and 65 years of age, with type 1 diabeted documented for more than 5 years, arginine stimulated C-peptide lower than 0.2ng/ml, and hypoglycemia awareness or documented metabolic lability. Exclusion criteria included body mass index greater than 28Kg/m2, unstable arteriopathy or heart disease, active infection, previous transplantation, insulin daily requirements above 1.2 UI/kg, creatinin clearance below 60 ml/mn/m2 or urinary albumin excretion above 300 mg/day, malignancy, smoking, desire for pregnancy, psychiatric disorders and lack of compliance. The study primary efficacy endpoint was graft survival defined as insulin independence and HbA1c<6.5%. Secondary outcomes were graft function and metabolic control.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

14

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Lille, Frankrig, 59037
        • University Hospital of Lille

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 65 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • type 1 diabetes documented for more than 5 years
  • arginine stimulated C-peptide lower than 0.2 ng/mL
  • one of the following:hypoglycemia unawareness OR metabolic lability documented by one or more severe hypoglycemias or two or more hospital admissions for ketoacidosis within the previous year.

Exclusion Criteria:

  • body mass index greater than 28 kg/m2
  • non stable arteriopathy or heart disease
  • active infection
  • previous transplantation
  • hyperimmunization
  • insulin daily needs above 1.2 U/Kg
  • creatinine clearance below 60 ml/mn or urinary albumin excretion above 300 mg/d
  • malignancy
  • smoking
  • desire for pregnancy
  • psychiatric disorders
  • lack of compliance

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: islet transplantation
Each participant received up to three sequential fresh islet infusions within three months.
Ø-transplantation bestod af op til tre sekventielle friske ø-infusioner inden for tre måneder. Adgang til portalvenen blev opnået under generel anæstesi ved perkutan kateterisering af en perifer portalgren under ultralydsvejledning eller ved kirurgisk kateterisering af en lille mesenterisk vene.
Andre navne:
  • kirurgisk kateterisation
  • perkutan kateterisation
Immunosuppressive consisted of Tacrolimus, target through level at 3-6 ng/ml, Sirolimus, target through level at 12-15 ng/ml for three months and at 7-10 ng/ml thereafter. A five-dose induction course of Daclizumab 1mg/Kg was administered biweekly beginning one hour prior to the first infusion
Andre navne:
  • Prograf
  • Rapamune
  • Zenapax

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Composite Criteria: Insulin Independence and Glycosylated Hemoglobin (HbA1c) Under 6.5% at One Year
Tidsramme: 1 year
The percentage of insulin independents subjects with an HbA1c less than 6.5% at one year after last transplant
1 year

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Hypoglycemic Events
Tidsramme: day 0 to day 365
Percentage of subjects free of severe hypoglycemic events from day 0 to day 365 with the day of transplant designated day 0
day 0 to day 365
Plasma C-peptide
Tidsramme: 1 year
Level of plasma C-peptide at 1 year after the first transplant
1 year
HbA1c < 6.5%
Tidsramme: 1 year
The percentage of subjects with HbA1c < 6.5% at 1 year after the first transplant
1 year
Percentage of Time Spent in Hypoglycemia (<0.70 mg/L)
Tidsramme: 1 year
percentage of time spent in hypoglycemia derived from CGMS (Continuous Glucose Monitoring System)
1 year
Number of Adverse Events
Tidsramme: 1 year
The number of adverse events related to the procedure and to the immunosuppression
1 year

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Francois Pattou, MD, University Hospital, Lille
  • Ledende efterforsker: Marie-Christine Vantyghem, MD PhD, University Hospital, Lille
  • Ledende efterforsker: Julie Kerr-Conte, PhD, Université de Lille 2

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. maj 2003

Primær færdiggørelse (Faktiske)

1. oktober 2007

Studieafslutning (Faktiske)

1. februar 2009

Datoer for studieregistrering

Først indsendt

9. marts 2007

Først indsendt, der opfyldte QC-kriterier

9. marts 2007

Først opslået (Skøn)

12. marts 2007

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

27. april 2012

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

23. april 2012

Sidst verificeret

1. februar 2009

Mere information

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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