RecruitingPhase 2NCT01889381

Human Craniomaxillofacial Allotransplantation


Sponsor

Johns Hopkins University

Enrollment

15 participants

Start Date

Aug 1, 2012

Study Type

INTERVENTIONAL

Conditions

Summary

Background: The human face is critically important for breathing, eating, seeing, and speaking/ communicating, but its most important job may be to look like a human face. Devastating facial deformities often cause affected individuals to avoid human contact and disappear from society. Although current surgical advancements can somewhat restore facial defects, this process often requires many operations and the resulting face only resembles the human face. To date, over 20 face transplants have been performed with highly encouraging functional and aesthetic results, but widespread clinical use has been limited due to the 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 face 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 face transplantation as a safe and effective reconstructive treatment for devastating injuries/ defects by minimizing maintenance immunosuppression therapy in face 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 15 full or partial human face transplants employing this novel protocol. Specific Aims: 1) To establish face transplantation as a safe and effective reconstructive strategy for the treatment of devastating facial injuries/defects; 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: Face transplantation could help injured individuals recover functionality, self-esteem, and the ability to reintegrate into family and social life as "whole" individuals. This 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 a wider clinical application of face transplantation.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study offers face and skull transplantation (craniomaxillofacial transplantation) to people with severe facial injuries or deformities that cannot be fully corrected with conventional reconstructive surgery. Researchers are investigating the safety, immune response, and functional outcomes of this complex procedure. You may be eligible if... - You have a significant craniomaxillofacial injury (recent or from years ago) - You are between 18 and 65 years old - You have a strong desire to undergo this procedure - You are a non-smoker (or have quit for more than 6 months) - You are a US citizen or equivalent - You are in good overall health with no active infections or cancer in the past 5 years - You have strong psychosocial support and can commit to the long-term treatment and follow-up You may NOT be eligible if... - You have active untreated infections, active HIV, tuberculosis, hepatitis, or active cancer - You have a history of medical non-compliance - You have high levels of antibodies against donor tissue (sensitized recipients) - You have connective tissue diseases or conditions that impair wound healing or nerve regeneration - You use IV drugs or have significant psychosocial problems such as alcoholism - Your psychiatric evaluation deems you unsuitable Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGBone marrow cell-based therapy & 1-drug immunosuppression.

This protocol uses a novel bone marrow cell-based therapy for composite tissue allotransplantation (CTA) rather than conventional triple-drug immunosuppression to facilitate long-term graft survival of deceased donor human faces under low-dose maintenance immunosuppression. Initial T-cell depletion with alemtuzumab is followed by upper extremity transplantation and tacrolimus maintenance therapy. Donor bone marrow cells are infused on Day 10 (±4 days) post-transplantation to elicit a host alloimmune response triggering exhaustion and deletion of the respective host (anti-donor) lymphocyte clones. Subsequently, tacrolimus therapy is given for at least 6 months before spaced weaning is considered in stable recipients.


Locations(1)

Johns Hopkins University School of Medicine

Baltimore, Maryland, United States

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NCT01889381


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