LUTX_phenotype: Biomolecular Phenotyping of Lung Transplant Recipients
Study Details
Study Description
Brief Summary
Primary graft dysfunction (PGD) is a common problem after a lung transplant. It's a sudden lung injury that affects around 30% of patients within 72 hours of getting a new lung. PGD can vary in severity, from mild issues seen on X-rays to severe lung problems, and it can also affect other parts of the body like the heart and kidneys.
We believe that using precision medicine, we can identify different groups of patients with varying levels of inflammation and provide them with treatments tailored to their specific condition. This approach has been successful in treating other serious conditions like acute respiratory distress syndrome (ARDS). Currently, we haven't classified lung transplant patients in this way, and there's limited information on early blood markers for PGD.
In an upcoming study, we aim to group lung transplant patients based on their blood markers related to inflammation, blood clotting, and blood vessel problems. We also want to see if these groups are linked to their overall outcomes, especially when it comes to PGD.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
Primary graft dysfunction (PGD) is the most common complication after lung transplant (LUTX). PGD is an acute form of lung injury with an incidence of 30%, defined upon alteration of oxygenation and radiographic criteria occurring <72 hours after graft reperfusion.
The PGD definition does not consider the heterogeneity of clinical manifestations of ischemia-reperfusion (I/R) injury. First, PGD severity may vary from mild radiographic signs to life-threatening lung injury. Second, duration may differ: most patients manifest transient hypoxia, but a minority have persistent respiratory failure. Finally, PGD is associated with hemodynamic and renal failure, suggesting that it might be considered a heterogeneous syndrome characterized by multisystemic widespread endothelial barrier damage and inflammation activation due to I/R injury rather than an alteration of the sole lung function.
Following the new paradigm of precision medicine, we hypothesize that predictive enrichment may allow for detecting different - and potentially treatable - traits (i.e., hypo vs. hyperinflammatory) of PGD and applying targeted treatments to sub-cohorts. As for other critical illnesses (i.e., acute respiratory distress syndrome - ARDS, sepsis), we envision the possibility of carrying out biological subtyping of LUTX patients to select the patients with the lowest chance of harm for treatment. In the similar -but not equivalent- context of ARDS, it has been proven that treatments (e.g., positive end-expiratory pressure, fluid management, simvastatin) that disappointingly failed to benefit the overall patients' population provided benefit in specific patients' subcohorts. Biological phenotyping of LUTX recipients has never been carried out, and literature is ample but sparse regarding early PGD plasmatic biomarkers.
With this prospective observational study, we aim to assess: 1/ whether LUTX recipients can be clustered based on early plasma concentration of biomarkers of inflammation, coagulation, and endothelial activation, and 2/ whether these clusters could be associated with clinical outcomes (and specifically PGD).
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Hypoinflammatory By means of latent class analysis, a sub-phenotype of LUTX recipients with down-regulated inflammatory biomarkers |
Diagnostic Test: Sub-phenotyping by biomarkers concentration
Plasma will be collected at ICU admission (i.e., < 6 hours from graft reperfusion), centrifuged (1500G for 15 min), frozen at -80°c, and then centralized at the Institutional laboratory. The following biomarkers will be assessed: sRAGE, SP-D, P-selectin (for alveolar damage); ICAM-1, IL6, IL8, IL10, TNF-alfa, IFN-gamma, CCL2, GM-CSF, TNFR1 (inflammation); angiopoietin-1, angiopoietin-2, TIMP-1 (endothelial damage). Analyses will be carried out on a Luminex platform (BioRad, Hercules, California, USA) - available at our Institution.
|
| Hyperinflammatory By means of latent class analysis, a sub-phenotype of LUTX recipients with up-regulated inflammatory biomarkers |
Diagnostic Test: Sub-phenotyping by biomarkers concentration
Plasma will be collected at ICU admission (i.e., < 6 hours from graft reperfusion), centrifuged (1500G for 15 min), frozen at -80°c, and then centralized at the Institutional laboratory. The following biomarkers will be assessed: sRAGE, SP-D, P-selectin (for alveolar damage); ICAM-1, IL6, IL8, IL10, TNF-alfa, IFN-gamma, CCL2, GM-CSF, TNFR1 (inflammation); angiopoietin-1, angiopoietin-2, TIMP-1 (endothelial damage). Analyses will be carried out on a Luminex platform (BioRad, Hercules, California, USA) - available at our Institution.
|
Outcome Measures
Primary Outcome Measures
- Primary Graft Dysfunction [<= 72 hours from graft reperfusion]
PGD incidence, defined and graded following the most recent ISHLT society guidelines, as hypoxia (i.e., PaO2/FiO2 < 300 mmHg) with bilateral lung infiltrates.
Secondary Outcome Measures
- 28-days organ support free-days [28 days from ICU admission]
Number of days at 28 days from ICU admission free from: - extracorporeal membrane oxygenation; - mechanical ventilation; - renal replacement therapy; - vasoactive support.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
undergone double LUTX
-
age > 18 years old
Exclusion Criteria:
-
single LUTX
-
re-transplantation
-
bridge-to-LUTX by extracorporeal membrane oxygenation
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Fondazione IRCCS Ca'Granda - Ospedale Maggiore Policlinico | Milan | Italy | 20122 |
Sponsors and Collaborators
- Policlinico Hospital
Investigators
- Study Director: Giacomo Grasselli, Porf, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
- Principal Investigator: Vittorio Scaravilli, MD, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- LUTX_phenotype