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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05934617
Other study ID # TRAJLUNG001
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date January 1, 2020
Est. completion date July 1, 2024

Study information

Verified date May 2024
Source Paris Translational Research Center for Organ Transplantation
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

For individuals with ESLD, lung transplantation is the best, or only treatment option with increased pulmonary function and quality of life. The forced expiratory volume in one second (FEV1) is the standard to monitor the lung function after transplantation. The goal of this study is to identify and validate the FEV1 trajectories after lung transplantation, as well as their determinants and outcomes, using an international cohort of lung recipients.


Description:

Chronic lung diseases affect about 500 million individuals and are the third leading cause of death worldwide, accounting for 7% of all mortality. They drive the growing number of individuals with end stage lung disease (ESLD), a public health issue with socioeconomic consequences. For individuals with ESLD, lung transplantation is the best, or only treatment option with increased pulmonary function and quality of life. Lung recipients remain however particularly at risk, with a median patient survival of around five years, which is much lower than other organ recipients, such as kidney, heart or liver recipients. Adequate monitoring of the lung recipient is therefore crucial to optimize the allograft longevity. The forced expiratory volume in one second (FEV1) is the standard to monitor the lung function after transplantation, and is used to evaluate the stage and severity of lung allograft diseases. However, according to a literature review we performed, the very few studies that have investigated the FEV1 evolution, and its relationship with outcomes such as death or chronic lung allograft dysfunction, were commonly based on cohort with insufficient data variety and completeness. Importantly, these studies lacked external validation, multidimensional approach, and none has attempted to identify the main profiles of FEV1 trajectories and their associated parameters. As such, the determinants and long-term outcomes of FEV1 trajectories are still poorly understood. A multidimensional, trajectory-based approach may help unveil clinically relevant organ function profiles among lung recipients. Indeed, several studies have shown the potential existence of underlying trajectories of transplanted organs' function and diseases, and their associations with outcomes and relevance for patient management, such as in kidney or heart transplantation. These studies used a unsupervised approach, which permitted to erase any preconceived clinical ideas. Overall, this approach has shown its value in several medical specialties, in particular in image analysis, oncology, or cardiology. Therefore, the goal of this study was to identify and validate the FEV1 trajectories after lung transplantation, as well as their determinants and outcomes, using an international cohort of lung recipients, with a protocol-based collection of FEV1 repeated assessments and clinical, biological, histological and immunological data.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 2500
Est. completion date July 1, 2024
Est. primary completion date January 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Double lung transplant recipients - Age 18 years or older at the time of transplant - Transplant between January 1, 2010 and December 31, 2020 - At least 2 PFTs available for analysis Exclusion Criteria: - Did not consent to clinical data use for research purposes - Multi-organ transplant

Study Design


Related Conditions & MeSH terms

  • Chronic Lung Allograft Dysfunction
  • Lung Transplant Failure and Rejection

Locations

Country Name City State
France Foch hospital Suresnes

Sponsors (1)

Lead Sponsor Collaborator
Paris Translational Research Center for Organ Transplantation

Country where clinical trial is conducted

France, 

References & Publications (4)

Brakema EA, Tabyshova A, van der Kleij RMJJ, Sooronbaev T, Lionis C, Anastasaki M, An PL, Nguyen LT, Kirenga B, Walusimbi S, Postma MJ, Chavannes NH, van Boven JFM; FRESH AIR collaborators. The socioeconomic burden of chronic lung disease in low-resource settings across the globe - an observational FRESH AIR study. Respir Res. 2019 Dec 21;20(1):291. doi: 10.1186/s12931-019-1255-z. — View Citation

GBD Chronic Respiratory Disease Collaborators. Prevalence and attributable health burden of chronic respiratory diseases, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet Respir Med. 2020 Jun;8(6):585-596. doi: 10.1016/S2213-2600(20)30105-3. — View Citation

Li X, Cao X, Guo M, Xie M, Liu X. Trends and risk factors of mortality and disability adjusted life years for chronic respiratory diseases from 1990 to 2017: systematic analysis for the Global Burden of Disease Study 2017. BMJ. 2020 Feb 19;368:m234. doi: 10.1136/bmj.m234. Erratum In: BMJ. 2020 Aug 6;370:m3150. — View Citation

Perch M, Hayes D Jr, Cherikh WS, Zuckermann A, Harhay MO, Hsich E, Potena L, Sadavarte A, Lindblad K, Singh TP, Stehlik J; International Society for Heart and Lung Transplantation. The International Thoracic Organ Transplant Registry of the International Society for Heart and Lung Transplantation: Thirty-ninth adult lung transplantation report-2022; focus on lung transplant recipients with chronic obstructive pulmonary disease. J Heart Lung Transplant. 2022 Oct;41(10):1335-1347. doi: 10.1016/j.healun.2022.08.007. Epub 2022 Aug 20. No abstract available. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary FEV1 trajectories FEV1 trajectories of the lung recipient Up to 10 years after lung transplantation
Secondary Patient death Patient death after lung transplantation Up to 10 years after lung transplantation
Secondary Allograft failure Allograft failure after lung transplantation Up to 10 years after lung transplantation
Secondary Chronic lung allograft dysfunction CLAD after lung transplantation Up to 10 years after lung transplantation
See also
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Active, not recruiting NCT03656926 - Efficacy + Safety of Liposome Cyclosporine A to Treat Bronchiolitis Obliterans Post Single Lung Transplant (BOSTON-2) Phase 3
Recruiting NCT04837339 - Diagnostic and Prognostic Biomarkers of Transplant Dysfunction in the Context of Lung Transplantation N/A
Terminated NCT04318587 - Assessment of Donor Derived Cell Free DNA and Utility in Lung Transplantation N/A
Enrolling by invitation NCT04787822 - Long Term Follow up of the LTOG Cohort
Active, not recruiting NCT04126746 - Clinical Trials in Organ Transplantation Extension Study
Active, not recruiting NCT03657342 - Efficacy + Safety of Liposome Cyclosporine A to Treat Bronchiolitis Obliterans Post Single Lung Transplant (BOSTON-1) Phase 3