Efficacy and Safety of Sirolimus in Lymphangioleiomyomatosis
University of Cincinnati Medical Center · University of Cincinnati · +20 more institutions
Abstract
Lymphangioleiomyomatosis (LAM) is a progressive, cystic lung disease in women; it is associated with inappropriate activation of mammalian target of rapamycin (mTOR) signaling, which regulates cellular growth and lymphangiogenesis. Sirolimus (also called rapamycin) inhibits mTOR and has shown promise in phase 1-2 trials involving patients with LAM.
We conducted a two-stage trial of sirolimus involving 89 patients with LAM who had moderate lung impairment--a 12-month randomized, double-blind comparison of sirolimus with placebo, followed by a 12-month observation period. The primary end point was the difference between the groups in the rate of change (slope) in forced expiratory volume in 1 second (FEV(1)).
Citation impact
- FWCI
- 44.45
- Percentile
- 100%
- References
- 27
Authors
25- FXFrancis X. McCormackCorresponding
University of Cincinnati Medical Center, University of Cincinnati
- YIYoshikazu Inoue
National Kinki Chuo Hospital for Chest Disease, National Hospital Organization
- JMJoel Moss
National Heart Lung and Blood Institute, National Institutes of Health
- LSL.G. Singer
University of Toronto
- CSCharlie Strange
Medical University of South Carolina
Topics & keywords
- Lymphangioleiomyomatosis
- Sirolimus
- Medicine
- Placebo
- Lung
- Urology
- Internal medicine
- Vital capacity
- Good health and well-being
Funding
- TSTuberous Sclerosis Alliance
- PPfizer
- LFLAM Foundation
- CCCincinnati Children's Hospital Medical Center
- NINational Institutes of HealthAwards: 1UL1RR026314, 1UL1RR026314-01
- CICanadian Institutes of Health Research
- NHNational Heart, Lung, and Blood Institute
- NCNational Center for Research ResourcesAwards: RR019498, 1UL1RR026314-01, RR019259
- NDNHLBI Division of Intramural Research