Pancreas Allograft Recipients w/wo Kidney TransplantationEXPANDNCT01384006
Extended Pancreas Donor Program - The EXPAND Study
An observational study of Pancreas Allograft Recipients w/wo Kidney Transplantation, run by University of Regensburg at 1 site in Germany.
Trial summary
To expand the donor pool for pancreas allografts. For detailed description please see below. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Pancreas Allograft Recipients w/wo Kidney Transplantation
- How many people
- 110 participants
- Where
- 1 siteGermany
- Study dates
- Jun 2011to Jun 2014
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Pancreas allograft recipients in Germany
Who may be able to join
- Recipients of standard allocation organs or
- Recipients of organs from donors between 50 to 60 years OR a BMI 30-34
- CIT (cold ischemic time) ≤ 12h (only local allocation of organs, optimally the procuring surgical team should be the transplanting team).
- and
- negative cross-match
- age > 18 years
- primary SPK, PAK or PTA
- Patients on standardized immunosuppressive treatment with Tacrolimus (Prograf®), MPA (Myfortic®) [aiming at center specific trough-level practice] from day 5 after transplantation (prior to day 5 MMF (Cell Cept®) can be applied as i.v. medication due to reduced gastrointestinal passage and insecure absorption of orally applied medication) and center-specific steroid treatment.
Who cannot join
- Malignant diseases within 5 years prior to PTA/SPK except for squamous cell carcinoma and basalioma of the skin.
- Pancreas retransplantation.
- Immunized patients with a preformed antibody titer>5%.
- Women with child bearing potential.
- Patients with a psychological, familial, sociologic or geographic condition potentially hampering compliance with the study protocol and follow-up schedule.
- Patients under guardianship (e.g. individuals who are not able to freely give their informed consent).
Trial locations and contacts
1 site in 1 country.
Germany1 site, 1 recruiting
- Recruiting
Regensburg University Hospital
Regensburg, Bavaria, 93053
Andrea Proneth, MD, +49-941-944 ext. 0, andrea.proneth@klinik.uni-r.de
Susanne Melter, +49-941-944 ext. 6770, susanne.melter@klinik.uni-r.de
About this study
Official title: EXTENDED PANCREAS DONOR PROGRAM - THE EXPAND STUDY
To expand the donor pool for pancreas allografts. For detailed description please see below.
Read the detailed description
This is an investigator initiated prospective, non-randomized feasibility-study, comparing recipients of EDC-pancreas allografts (SPK or PTA) with patients undergoing SPK or PTA with standard criteria allografts.
Simultaneous Pancreas Kidney transplantation (SPK) or Pancreas Transplantation alone (PTA) are life saving procedures for patients with type 1 (juvenile) diabetes mellitus and impaired renal function. Although the waiting lists for SPK and PTA are increasing, the numbers of pancreas transplantations are declining in the Eurotransplant (ET) area (www.eurotransplant.nl). One major reason for this decline is the fact that a large number of pancreas allografts, potentially eligible for transplantation are excluded by the ET pancreas allocation system (EPAS). Those criteria include an organ-specific cut-off for donor age >50 years and/or BMI>30. This means that donors that are older than 50 years or donors with a BMI >30 are, at the moment, not considered for solid organ transplantation. The pancreas will be directly allocated for islet transplantation (Eurotransplant manual - version may 26, 2009).
The organ-specific cut-off was once established to provide donor pancreases for islet transplantation. Although 173 pancreases were allocated and retrieved for islet transplantation only 17 islet transplantations were performed in the whole ET area in 2008 (ET data). In Germany two islet transplantations were performed in 2009. Best results after islet transplantation are achieved with organs obtained from young obese donors. Concerning allocation, no conflict of interest exists between whole organ and islet transplantation, the single active German islet center will take part in the EXPAND study. Meanwhile, according to the suggestions by the EXPAND study group, extended donor pancreases are intended to be offered regionally as "rescue" allocation to the centers. The centers should then decide if this organ can be transplanted as whole organ or if it can be used for islets.
As the average age for a post mortal organ donor in the ET area is now 58 years, there is a severe donor selection by age leading to organ shortage. In Germany in 2008 the total number of organ donors was 1.198. However, only 510 donors had an age between 3 and 50 years and thus were potentially eligible for pancreas donation. Out of the 510 donors only 183 pancreases (36% of all potential, age restricted pancreas donors) were retrieved and 127 (25%) were transplanted (DSO, Deutsche Stiftung für Organtransplantation e.V.). Altogether, 676 donors were not even screened for pancreas donation due to age, regardless to all other medical conditions. In addition, approximately 13% were not eligible for pancreas donation only due to BMI. Moreover, in the ET-area pancreases are allocated without local priority leading to longer ischemic times due to transport ways. However, there are data from other allocation areas throughout the world (UNOS or UK) showing that a good overall outcome after PTx can be achieved with donors exceeding the defined allocation criteria defined by ET (older than 50 or BMI>30), if the cold ischemic time is kept short. In Great Britain, a local retrieval and allocation system was installed in 2000 resulting in a steep increase in pancreas transplantation. Moreover, within this new allocation system the currently worldwide largest and most successful pancreas transplant program was initiated in Oxford in 2004 with an extensive use of extended pancreas donors leading to excellent results. These extended criteria avoided donor BMI restriction, and accepted donors with an age between 8 and 68 years. Meanwhile 350 SPK and PTA were transplanted with an excellent one year pancreas survival of 91%, kidney survival 95% and a patient survival of 96%.
In the US, a retrospective analysis of OPTN registries compared 8.850 SPK from young donors vs. 776 SPK from donors >45 years. It showed that patients transplanted from an older donor have equal survival compared to those who were waiting for a young donor for more than 1.5 years. However the earlier transplanted patient is instantly off dialysis and insulin. Good results were already achieved with extended pancreas donors in the US and also in one German study.
Based on those findings, a new pancreas allocation system was established in the USA where standard pancreases (donor age < 50y or BMI < 30) are allocated first on local, then on regional and then on national levels and extended pancreas (donor age > 50 years or BMI > 30) are allocated locally only.
In conclusion, these data indicate the requirement for a new allocation system also in the ET area to be able to provide a sufficient number of organs for patients on the waiting list. We therefore suggest a new pancreas allocation system where donors with an age of 50-60 years or a BMI of 30-34 are allocated regionally within a cold ischemic time < 12 h. To prove the hypothesis that extended pancreas allograft donors can be used safely with equal outcome in recipients a prospective comparative multicenter feasibility-study is required.
A good example of a successful change of allocation rules is the European Senior Donor Program (ESDP) for kidneys, the so called "old for old" program. Within this program kidneys from donors >65 years are allocated regionally to patients >65 years with a relatively short ischemic time without HLA matching. For this purpose a comparative study was performed to prove the efficacy of this allocation change.
The standard immunosuppression for SPK or PTA includes induction therapy with antibodies. Maintenance therapy is mostly performed with a tacrolimus / mycophenolate mofetil combination. The usage of calcineurin inhibitors for maintenance therapy is characterized by a clear transition from cyclosporine to tacrolimus. Myfortic® vs. Cell Cept® shows beneficial effects after SPK in a large single center comparison. Corticosteroids are administered to the majority of patients; however, steroid-avoidance and steroid-withdrawal protocols are increasingly common.
- Keywords
- Pancreas transplantation, extended donor criteria, organ survival
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Control | standard pancreas allograft recipients | |
| Study | recipients of extended donor criteria pancreas allografts |
What is being measured
The primary outcome is the main question the study is designed to answer.
Pancreas allograft survival at 3 months after transplantation
Pancreas allograft survival at 3 months after transplantation has been defined as primary endpoint. Patients that are insulin-free and have a normal fasting glucose level 60 - 140 mg/dl (3.3 - 7.8 mmol/l) in peripheral venous blood are regarded as having a functioning organ. Thus, all patients that have a pathologic fasting glucose level at 3 months will be counted as event with regards to the primary endpoint of pancreas allograft survival.
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Jun 2011 (estimated)
- Study startJun 2011
- Primary completionJun 2013 (estimated)
- Study completionJun 2014 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Pancreas Allograft Recipients w/wo Kidney TransplantationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Time perspective
- Prospective
- Enrolment
- 110 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Regensburg
- Sponsor type
- University, hospital or other
- Collaborators
- Charite University, Berlin, Germany, Ludwig-Maximilians - University of Munich, University of Jena, Johann Wolfgang Goethe University Hospital, University Hospital Tuebingen, University Hospital Erlangen, University of Heidelberg Medical Center, University of Leipzig, University Hospital Dresden, University Hospital Bergmannsheil Bochum, Hannover Medical School, Universitätsklinikum Hamburg-Eppendorf, University of Kiel, Transplantationszentrum Köln-Merheim
- Investigators
- Stefan A Farkas, MD, Study director, Regensburg Univeristy HospitalAndreas A Schnitzbauer, MD, Principal investigator, Regensburg University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01384006
- Sponsor's protocol ID
- EXPAND
- Acronym
- EXPAND
- Status last verified
- Jun 2011
- First submitted
- 27 Jun 2011
- Last updated
- 4 Jul 2011
- Results posted
- No
- Data monitoring committee
- Yes
Publications
Proneth A, Schnitzbauer AA, Schenker P, Wunsch A, Rauchfuss F, Arbogast H, Manekeller S, Nadalin S, Heise M, Strohlein MA, Banas B, Schemmer P, Becker T, Bechstein WO, Pascher A, Viebahn R, Geissler EK, Schlitt HJ, Farkas SA. Extended Pancreas Donor Program-The EXPAND Study: A Prospective Multicenter Trial Testing the Use of Pancreas Donors Older Than 50 Years. Transplantation. 2018 Aug;102(8):1330-1337. doi: 10.1097/TP.0000000000002122.
PubMed 29406443Proneth A, Schnitzbauer AA, Zeman F, Foerster JR, Holub I, Arbogast H, Bechstein WO, Becker T, Dietz C, Guba M, Heise M, Jonas S, Kersting S, Klempnauer J, Manekeller S, Muller V, Nadalin S, Nashan B, Pascher A, Rauchfuss F, Strohlein MA, Schemmer P, Schenker P, Thorban S, Vogel T, Rahmel AO, Viebahn R, Banas B, Geissler EK, Schlitt HJ, Farkas SA. Extended pancreas donor program - the EXPAND study rationale and study protocol. Transplant Res. 2013 Jul 1;2(1):12. doi: 10.1186/2047-1440-2-12.
PubMed 23816330
Study at a glance
From the registry record, last updated by the sponsor on 4 Jul 2011. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- EXTENDED PANCREAS DONOR PROGRAM - THE EXPAND STUDY
- ClinicalTrials.gov ID
- NCT01384006
- Acronym / sponsor ID
- EXPAND / EXPAND
- Keywords
- Pancreas transplantation, extended donor criteria, organ survival
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 110 participants (estimated)
- Lead sponsor
- University of RegensburgUniversity, hospital or other
- Collaborators
- Charite University, Berlin, Germany, Ludwig-Maximilians - University of Munich, University of Jena, Johann Wolfgang Goethe University Hospital, University Hospital Tuebingen, University Hospital Erlangen, University of Heidelberg Medical Center, University of Leipzig, University Hospital Dresden, University Hospital Bergmannsheil Bochum, Hannover Medical School, Universitätsklinikum Hamburg-Eppendorf, University of Kiel, Transplantationszentrum Köln-Merheim
- Study start
- Jun 2011
- Primary completion
- Jun 2013 (estimated)
- Study completion
- Jun 2014 (estimated)
- First posted
- 28 Jun 2011 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To expand the donor pool for pancreas allografts. For detailed description please see below.
Detailed description
This is an investigator initiated prospective, non-randomized feasibility-study, comparing recipients of EDC-pancreas allografts (SPK or PTA) with patients undergoing SPK or PTA with standard criteria allografts.
Simultaneous Pancreas Kidney transplantation (SPK) or Pancreas Transplantation alone (PTA) are life saving procedures for patients with type 1 (juvenile) diabetes mellitus and impaired renal function. Although the waiting lists for SPK and PTA are increasing, the numbers of pancreas transplantations are declining in the Eurotransplant (ET) area (www.eurotransplant.nl). One major reason for this decline is the fact that a large number of pancreas allografts, potentially eligible for transplantation are excluded by the ET pancreas allocation system (EPAS). Those criteria include an organ-specific cut-off for donor age >50 years and/or BMI>30. This means that donors that are older than 50 years or donors with a BMI >30 are, at the moment, not considered for solid organ transplantation. The pancreas will be directly allocated for islet transplantation (Eurotransplant manual - version may 26, 2009).
The organ-specific cut-off was once established to provide donor pancreases for islet transplantation. Although 173 pancreases were allocated and retrieved for islet transplantation only 17 islet transplantations were performed in the whole ET area in 2008 (ET data). In Germany two islet transplantations were performed in 2009. Best results after islet transplantation are achieved with organs obtained from young obese donors. Concerning allocation, no conflict of interest exists between whole organ and islet transplantation, the single active German islet center will take part in the EXPAND study. Meanwhile, according to the suggestions by the EXPAND study group, extended donor pancreases are intended to be offered regionally as "rescue" allocation to the centers. The centers should then decide if this organ can be transplanted as whole organ or if it can be used for islets.
As the average age for a post mortal organ donor in the ET area is now 58 years, there is a severe donor selection by age leading to organ shortage. In Germany in 2008 the total number of organ donors was 1.198. However, only 510 donors had an age between 3 and 50 years and thus were potentially eligible for pancreas donation. Out of the 510 donors only 183 pancreases (36% of all potential, age restricted pancreas donors) were retrieved and 127 (25%) were transplanted (DSO, Deutsche Stiftung für Organtransplantation e.V.). Altogether, 676 donors were not even screened for pancreas donation due to age, regardless to all other medical conditions. In addition, approximately 13% were not eligible for pancreas donation only due to BMI. Moreover, in the ET-area pancreases are allocated without local priority leading to longer ischemic times due to transport ways. However, there are data from other allocation areas throughout the world (UNOS or UK) showing that a good overall outcome after PTx can be achieved with donors exceeding the defined allocation criteria defined by ET (older than 50 or BMI>30), if the cold ischemic time is kept short. In Great Britain, a local retrieval and allocation system was installed in 2000 resulting in a steep increase in pancreas transplantation. Moreover, within this new allocation system the currently worldwide largest and most successful pancreas transplant program was initiated in Oxford in 2004 with an extensive use of extended pancreas donors leading to excellent results. These extended criteria avoided donor BMI restriction, and accepted donors with an age between 8 and 68 years. Meanwhile 350 SPK and PTA were transplanted with an excellent one year pancreas survival of 91%, kidney survival 95% and a patient survival of 96%.
In the US, a retrospective analysis of OPTN registries compared 8.850 SPK from young donors vs. 776 SPK from donors >45 years. It showed that patients transplanted from an older donor have equal survival compared to those who were waiting for a young donor for more than 1.5 years. However the earlier transplanted patient is instantly off dialysis and insulin. Good results were already achieved with extended pancreas donors in the US and also in one German study.
Based on those findings, a new pancreas allocation system was established in the USA where standard pancreases (donor age < 50y or BMI < 30) are allocated first on local, then on regional and then on national levels and extended pancreas (donor age > 50 years or BMI > 30) are allocated locally only.
In conclusion, these data indicate the requirement for a new allocation system also in the ET area to be able to provide a sufficient number of organs for patients on the waiting list. We therefore suggest a new pancreas allocation system where donors with an age of 50-60 years or a BMI of 30-34 are allocated regionally within a cold ischemic time < 12 h. To prove the hypothesis that extended pancreas allograft donors can be used safely with equal outcome in recipients a prospective comparative multicenter feasibility-study is required.
A good example of a successful change of allocation rules is the European Senior Donor Program (ESDP) for kidneys, the so called "old for old" program. Within this program kidneys from donors >65 years are allocated regionally to patients >65 years with a relatively short ischemic time without HLA matching. For this purpose a comparative study was performed to prove the efficacy of this allocation change.
The standard immunosuppression for SPK or PTA includes induction therapy with antibodies. Maintenance therapy is mostly performed with a tacrolimus / mycophenolate mofetil combination. The usage of calcineurin inhibitors for maintenance therapy is characterized by a clear transition from cyclosporine to tacrolimus. Myfortic® vs. Cell Cept® shows beneficial effects after SPK in a large single center comparison. Corticosteroids are administered to the majority of patients; however, steroid-avoidance and steroid-withdrawal protocols are increasingly common.
Study design
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Control | – | –standard pancreas allograft recipients |
| Study | – | –recipients of extended donor criteria pancreas allografts |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Pancreas allograft recipients in Germany
Key inclusion criteria (8 listed)
- Recipients of standard allocation organs or
- Recipients of organs from donors between 50 to 60 years OR a BMI 30-34
- CIT (cold ischemic time) ≤ 12h (only local allocation of organs, optimally the procuring surgical team should be the transplanting team).
- and
- negative cross-match
Key exclusion criteria (6 listed)
- Malignant diseases within 5 years prior to PTA/SPK except for squamous cell carcinoma and basalioma of the skin.
- Pancreas retransplantation.
- Immunized patients with a preformed antibody titer>5%.
- Women with child bearing potential.
- Patients with a psychological, familial, sociologic or geographic condition potentially hampering compliance with the study protocol and follow-up schedule.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Pancreas allograft survival at 3 months after transplantation
Time frame: 3 months
Pancreas allograft survival at 3 months after transplantation has been defined as primary endpoint. Patients that are insulin-free and have a normal fasting glucose level 60 - 140 mg/dl (3.3 - 7.8 mmol/l) in peripheral venous blood are regarded as having a functioning organ. Thus, all patients that have a pathologic fasting glucose level at 3 months will be counted as event with regards to the primary endpoint of pancreas allograft survival.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Jul 2011.
- Derived from this study: PubMed 29406443Proneth A, Schnitzbauer AA, Schenker P, Wunsch A, Rauchfuss F, Arbogast H, Manekeller S, Nadalin S, Heise M, Strohlein MA, Banas B, Schemmer P, Becker T, Bechstein WO, Pascher A, Viebahn R, Geissler EK, Schlitt HJ, Farkas SA. Extended Pancreas Donor Program-The EXPAND Study: A Prospective Multicenter Trial Testing the Use of Pancreas Donors Older Than 50 Years. Transplantation. 2018 Aug;102(8):1330-1337. doi: 10.1097/TP.0000000000002122.
- Derived from this study: PubMed 23816330Proneth A, Schnitzbauer AA, Zeman F, Foerster JR, Holub I, Arbogast H, Bechstein WO, Becker T, Dietz C, Guba M, Heise M, Jonas S, Kersting S, Klempnauer J, Manekeller S, Muller V, Nadalin S, Nashan B, Pascher A, Rauchfuss F, Strohlein MA, Schemmer P, Schenker P, Thorban S, Vogel T, Rahmel AO, Viebahn R, Banas B, Geissler EK, Schlitt HJ, Farkas SA. Extended pancreas donor program - the EXPAND study rationale and study protocol. Transplant Res. 2013 Jul 1;2(1):12. doi: 10.1186/2047-1440-2-12.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Stefan A Farkas, MD study director
Regensburg Univeristy Hospital
Andreas A Schnitzbauer, MD principal investigator
Regensburg University Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Pancreas Allograft Recipients w/wo Kidney Transplantation, run by University of Regensburg at 1 site in Germany.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 8 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 4 Jul 2011. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Stefan A Farkas, MD (+49-941-944 ext. 6813, stefan.farkas@klinik.uni-r.de), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Pancreas allograft survival at 3 months after transplantation (time frame: 3 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01384006, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Jul 2011; AzTrials last refreshed its copy on 1 Nov 2026.