Does the duration of exposure to everolimus influence the occurrence of chronic lung allograft dysfunction?
What this study shows
In lung transplant recipients, later introduction of everolimus and a greater number of treatment interruptions were both risk factors for chronic lung allograft dysfunction; earlier, uninterrupted treatment was associated with lower CLAD risk (retrospective, single-centre; causality not established).
At a glance
| Evidence type | H Human study Marked H because it is direct evidence from a human clinical trial or human cohort; the code names the kind of study, not its quality -- a small, well-run trial is still H. |
| Study type | 3 - Human Observational |
| Model system | Human (single-centre retrospective observational) |
| Journal | Transplant Immunology |
| Year | 2026 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1016/j.trim.2026.102436 · PMID 42648493 |
Extracted findings
These fields were extracted from the paper with AI assistance and have not been checked against the source. Read them as a pointer into the paper, not as curated claims; where they disagree with the curated summary above, the curated summary stands.
| Intervention | Everolimus |
| Target | mTOR |
| Model | Human |
| Effect | Early introduction and fewer interruptions associated with lower CLAD risk; lung function stability maintained |
In the Atlas
Related topics
More studies on this topic
- Everolimus in postmenopausal hormone-receptor-positive advanced breast cancer (BOLERO-2) (2012)
- Everolimus for angiomyolipoma associated with tuberous sclerosis complex or sporadic lymphangioleiomyomatosis (EXIST-2): a multicentre, randomised, double-blind, placebo-controlled trial (2013)
- Efficacy and safety of everolimus for subependymal giant cell astrocytomas associated with tuberous sclerosis complex (EXIST-1): a multicentre, randomised, placebo-controlled phase 3 trial (2013)
- Adjunctive everolimus therapy for treatment-resistant focal-onset seizures associated with tuberous sclerosis (EXIST-3): a phase 3, randomised, double-blind, placebo-controlled study (2016)
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