Graft Rejection, Lung Disease
Conditions
Keywords
allograft, rejection, biopsy, gene, expression, pulmonary, lung, transplant
Brief summary
The objective of the LARGO Study protocol is to collect peripheral blood samples, select associated lung biopsy pathology slides, and clinical data from lung transplant recipients to perform molecular analyses in association with the study endpoints. The primary objective is to use gene expression profiling of peripheral blood mononuclear cells to differentiate between the absence and presence of acute cellular rejection. The secondary objectives are to use other genomic and proteomic technologies to analyze RNA and protein in blood samples in relation to related clinical conditions. The overall goal is to apply novel molecular insights in the development of non-invasive molecular diagnostic tests for lung transplantation.
Detailed description
LARGO is a prospective, multi-center, international observational study with participating centers in the United States, Canada and Europe. The target enrollment for study completion is 2,100 subjects. At each study visit, blood specimens are collected from subjects, processed and stored in the sample archive, with corresponding patient information entered into the clinical database. The analysis plan for each study objective includes a defined sample selection protocol that stipulates the inclusion and exclusion criteria for both patients and samples, and also the required number of blood specimens for the molecular analyses to achieve statistical significance. The diagnosis and treatment of acute cellular rejection remains a clinical management priority that is currently based on transbronchial biopsy. Gene expression profiling is a technology based on molecular biology that measures changes in the RNA levels of different genes expressed by circulating mononuclear cells in the peripheral blood. A key goal of the project is to use gene expression profiling to differentiate between the absence and presence of lung allograft acute cellular rejection, with the aim of using this novel information to develop a non-invasive diagnostic testing alternative.
Interventions
OTHERNon-interventional
Post-transplantation observational study
Sponsors
XDx
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
Yes
Inclusion criteria
* Lung and heart-lung transplant recipients who consent to participate and have transbronchial biopsy at the enrolling center during the study period
Exclusion criteria
* None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Infections other than CMV, e.g. bacterial, other viral, and fungal infections. | Scheduled clinic visit |
| Rejection episodes of at least moderate histologic grade which resulted in treatment of the patient with additional corticosteroids, anti-T cell antibodies, or total lymphoid irradiation. | Scheduled clinic visit |
| Obliterative Bronchiolitis diagnosed pathologically by biopsy or by a progressive decline in pulmonary function tests consistent with a diagnosis of Bronchiolitis Obliterans Syndrome (BOS). | Scheduled clinic visit |
| Allograft function as determined via pulmonary function tests. | Scheduled clinic visit |
| The absence of histologic rejection and normal or unchanged allograft function. | Scheduled clinic visit |
| Documented CMV infection by culture, histology, or PCR, and at least one clinical sign or symptom of infection. | Scheduled clinic visit |
Secondary
| Measure | Time frame |
|---|---|
| Rejection of mild to moderate histologic severity prompting augmentation of the patient's chronic immunosuppressive regimen. | Scheduled clinic visit |
| Allograft dysfunction during the study period. | Scheduled clinic visit |
| Rejection of mild to moderate severity with allograft dysfunction prompting plasmapheresis or a diagnosis of humoral rejection. | Scheduled clinic visit |
| Lymphoproliferative disorder (aka post-transplant lymphoma). | Scheduled clinic visit |
| Graft Failure or Retransplantation. | Scheduled clinic visit |
| All cause mortality. | Scheduled clinic visit |
Countries
Austria, Canada, Germany, United Kingdom, United States
Outcome results
None listed