RECRUITING

Human Upper Extremity Allotransplantation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Background: Millions of people each year sustain injuries, have tumors surgically removed, or are born with defects that require complex reconstructive surgeries to repair. In the case of hand, forearm, or arm amputation, prostheses only provide less than optimal motor function and no sensory feedback. However, hand and arm transplantation is a means to restore the appearance, anatomy, and function of a native hand. Although over 70 hand transplants have been performed to date and good functional results have been achieved, widespread clinical use has been limited due to adverse effects of life-long and high-dose immunosuppression needed to prevent graft rejection. Risks include infection, cancer, and metabolic problems, all of which can greatly affect recipients' quality of life, make the procedure riskier, and jeopardize the potential benefits of hand transplantation. Study Design: This non-randomized, Phase II clinical trial will document the use of a new immunomodulatory protocol (aka - Pittsburgh Protocol, Starzl Protocol) for establishing hand transplantation as a safe and effective reconstructive treatment for upper extremity amputations by minimizing maintenance immunosuppression therapy in unilateral and bilateral hand/forearm transplant patients. This protocol combines lymphocyte depletion with donor bone marrow cell infusion and has enabled graft survival using low doses of a single immunosuppressive drug followed by weaning of treatment. Initially designed for living-related solid organ donation, this regimen has been adapted for use with grafts donated by deceased donors. The investigators propose to perform 30 human hand transplants employing this novel protocol. Specific Aims: 1) To establish hand transplantation as a safe and effective reconstructive strategy for the treatment of upper extremity amputations; 2) To reduce the risk of rejection and enable allograft survival while minimizing the requirement for long-term high dose multi-drug immunosuppression. Significance of Research: Hand transplantation could help upper extremity amputees recover functionality, self-esteem, and the capability to reintegrate into family and social life as "whole" individuals. The protocol offers the potential for minimizing the morbidity of maintenance immunosuppression, thereby beneficially shifting the risk/benefit ratio of this life-enhancing procedure and enabling widespread clinical application of hand transplantation.

Official Title

Human Upper Extremity Allotransplantation

Quick Facts

Study Start:2011-07
Study Completion:2036-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT01459107

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 69 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Recent (≥6 months) or remote (i.e., several decades) unilateral or bilateral upper limb loss (below the shoulder) desiring limb transplantation.
  2. * Below-shoulder amputation.
  3. * Functionless or minimally functional hand desiring removal of functionless / minimally functional hand followed by transplantation.
  4. * Male or female and of any race, color or ethnicity.
  5. * Aged 18-69 years.
  6. * Completes the protocol informed consent form.
  7. * No co-existing medical condition which, in the opinion of the study team, could affect the immunomodulatory protocol, surgical procedure, or functional results (see Donor and Recipient Exclusion Criteria below. If the condition is amenable to treatment, the study team must agree that said condition should not significantly enhance the surgical risks of upper extremity transplantation.)
  8. * No co-existing psycho-social problems (i.e., alcoholism, drug abuse).
  9. * Negative for malignancy for past 5 years.
  10. * Negative for HIV at transplant.
  11. * Negative crossmatch with donor.
  12. * If female of child-bearing potential, negative serum pregnancy test.
  13. * If female of child-bearing potential, consent to use reliable contraception for at least one year following transplantation.
  14. * Consents to bone marrow infusion as part of the treatment regime.
  15. * USA citizen or equivalent, or foreigner with documentation of ability to pay for transplant and required follow-up care.
  16. * Patient agrees to comply with the protocol and states a dedication to the immunomodulatory treatment regime.
  1. * Untreated sepsis.
  2. * HIV (active or seropositive).
  3. * Active tuberculosis.
  4. * Hepatitis B or C.
  5. * Viral encephalitis.
  6. * Toxoplasmosis.
  7. * Malignancy (within past 5 years).
  8. * Current/recent (within 3 months of donation/screening consent) IV drug abuse.
  9. * Paralysis of ischemic or traumatic origin.
  10. * Inherited peripheral neuropathy.
  11. * Infectious, post infectious, or inflammatory (axonal or demyelinating) neuropathy.
  12. * Toxic neuropathy (i.e. heavy metal poisoning, drug toxicity, industrial agent exposure).
  13. * Mixed connective tissue disease.
  14. * Severe deforming rheumatoid or osteoarthritis in the limb.
  15. * Non-professional tattoo within last 6 months, or
  16. * Personally identifiable tattoo (i.e., donor name) on potential transplant.
  17. * Type I (insulin-dependent) diabetes mellitus
  18. * Conditions that, in the opinion of the study team, may impact the immunomodulatory protocol potentially exposing the recipient to an unacceptable risk under immunosuppressive treatment.
  19. * Sensitized recipients with high levels (50%) of panel-reactive human leukocyte antigen (HLA) antibodies.
  20. * Conditions that may impact the success of the surgical procedure or increase the risk of postoperative complications including inherited coagulopathies like Hemophilia, Von-Willebrand's disease, Protein C and S deficiency, Thrombocythemias, Thalassemias, Sickle Cell disease, etc.
  21. * Mixed connective tissue diseases and collagen diseases can result in poor wound healing after surgery.
  22. * Conditions that may impact functional outcomes including Lipopolysaccharidosis and amyloidosis (may impact nerve regeneration) or rare disorders of bone healing like osteopetrosis.
  23. * Patients considered unsuitable per the consulted Psychiatrists appraisal.

Contacts and Locations

Study Contact

Jane Littleton, CRNP, MSN
CONTACT
410-955-6875
jlittl38@jhmi.edu
TBD TBD
CONTACT
443-287-7848

Principal Investigator

Jaimie Shores, MD
PRINCIPAL_INVESTIGATOR
Johns Hopkins University

Study Locations (Sites)

Johns Hopkins University School of Medicine
Baltimore, Maryland, 21287
United States

Collaborators and Investigators

Sponsor: Johns Hopkins University

  • Jaimie Shores, MD, PRINCIPAL_INVESTIGATOR, Johns Hopkins University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2011-07
Study Completion Date2036-06

Study Record Updates

Study Start Date2011-07
Study Completion Date2036-06

Terms related to this study

Keywords Provided by Researchers

  • Hand Transplant
  • Composite Tissue Allotransplantation (CTA)
  • Vascularized Composite Allotransplantation (VCA)
  • Composite Tissue
  • Amputation
  • Upper limb
  • Immunosuppression

Additional Relevant MeSH Terms

  • Amputation, Traumatic
  • Wounds and Injuries
  • Hand Injuries