Lung function response and side effects to rapamycin for lymphangioleiomyomatosis: a prospective national cohort study

Rationale Mechanistic target of rapamycin inhibitors reduce loss of lung function in lymphangioleiomyomatosis (LAM), although their benefit varies between individuals. We examined lung function response and side effects to rapamycin in a national cohort. Methods Subjects were receiving ra...

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Main Authors: Bee, Janet, Fuller, Sharon, Miller, Suzanne, Johnson, Simon R.
Format: Article
Published: BMJ Publishing Group 2017
Online Access:https://eprints.nottingham.ac.uk/47947/
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author Bee, Janet
Fuller, Sharon
Miller, Suzanne
Johnson, Simon R.
author_facet Bee, Janet
Fuller, Sharon
Miller, Suzanne
Johnson, Simon R.
author_sort Bee, Janet
building Nottingham Research Data Repository
collection Online Access
description Rationale Mechanistic target of rapamycin inhibitors reduce loss of lung function in lymphangioleiomyomatosis (LAM), although their benefit varies between individuals. We examined lung function response and side effects to rapamycin in a national cohort. Methods Subjects were receiving rapamycin for progressive lung disease. Clinical evaluation, detailed phenotyping, serial lung function, rapamycin and safety monitoring were performed according to a clinical protocol. Lung function change, measured as FEV1 slope (ΔFEV1), was reported for those treated for 1 year or longer. Results Rapamycin was associated with improved ΔFEV1 in 21 individuals where pretreatment data were available (p<0.0001). In 47 treated for a mean duration of 35.8 months, mean ΔFEV1 was +11 (SD 75) mL/year, although it varied from +254 to −148 mL/year. The quartile with the highest positive ΔFEV1 had greater pretreatment FEV1 (p=0.02) and shorter disease durations (p=0.02) than the lowest quartile. Serum rapamycin level was positively associated with side effects (p=0.02) but not ΔFEV1 over 1 year. Within the first month of therapy, apthous ulcers, nausea and diarrhoea were associated with higher rapamycin levels. Acne, oedema and menstrual irregularities tended to increase over the first year of therapy. At the end of observation, the prevalence of side effects was 5% or less. Conclusions Rapamycin reduces lung function loss in LAM, although in some, ΔFEV1 continues to fall at an accelerated rate. Poor response to rapamycin was associated with lower pretreatment lung function and longer disease duration but not serum level. Early intervention with low-dose rapamycin may preserve lung function and reduce side effects.
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spelling nottingham-479472024-08-15T15:24:27Z https://eprints.nottingham.ac.uk/47947/ Lung function response and side effects to rapamycin for lymphangioleiomyomatosis: a prospective national cohort study Bee, Janet Fuller, Sharon Miller, Suzanne Johnson, Simon R. Rationale Mechanistic target of rapamycin inhibitors reduce loss of lung function in lymphangioleiomyomatosis (LAM), although their benefit varies between individuals. We examined lung function response and side effects to rapamycin in a national cohort. Methods Subjects were receiving rapamycin for progressive lung disease. Clinical evaluation, detailed phenotyping, serial lung function, rapamycin and safety monitoring were performed according to a clinical protocol. Lung function change, measured as FEV1 slope (ΔFEV1), was reported for those treated for 1 year or longer. Results Rapamycin was associated with improved ΔFEV1 in 21 individuals where pretreatment data were available (p<0.0001). In 47 treated for a mean duration of 35.8 months, mean ΔFEV1 was +11 (SD 75) mL/year, although it varied from +254 to −148 mL/year. The quartile with the highest positive ΔFEV1 had greater pretreatment FEV1 (p=0.02) and shorter disease durations (p=0.02) than the lowest quartile. Serum rapamycin level was positively associated with side effects (p=0.02) but not ΔFEV1 over 1 year. Within the first month of therapy, apthous ulcers, nausea and diarrhoea were associated with higher rapamycin levels. Acne, oedema and menstrual irregularities tended to increase over the first year of therapy. At the end of observation, the prevalence of side effects was 5% or less. Conclusions Rapamycin reduces lung function loss in LAM, although in some, ΔFEV1 continues to fall at an accelerated rate. Poor response to rapamycin was associated with lower pretreatment lung function and longer disease duration but not serum level. Early intervention with low-dose rapamycin may preserve lung function and reduce side effects. BMJ Publishing Group 2017-10-09 Article PeerReviewed Bee, Janet, Fuller, Sharon, Miller, Suzanne and Johnson, Simon R. (2017) Lung function response and side effects to rapamycin for lymphangioleiomyomatosis: a prospective national cohort study. Thorax . ISSN 0040-6376 https://doi.org/10.1136/thoraxjnl-2017-210872 doi:10.1136/thoraxjnl-2017-210872 doi:10.1136/thoraxjnl-2017-210872
spellingShingle Bee, Janet
Fuller, Sharon
Miller, Suzanne
Johnson, Simon R.
Lung function response and side effects to rapamycin for lymphangioleiomyomatosis: a prospective national cohort study
title Lung function response and side effects to rapamycin for lymphangioleiomyomatosis: a prospective national cohort study
title_full Lung function response and side effects to rapamycin for lymphangioleiomyomatosis: a prospective national cohort study
title_fullStr Lung function response and side effects to rapamycin for lymphangioleiomyomatosis: a prospective national cohort study
title_full_unstemmed Lung function response and side effects to rapamycin for lymphangioleiomyomatosis: a prospective national cohort study
title_short Lung function response and side effects to rapamycin for lymphangioleiomyomatosis: a prospective national cohort study
title_sort lung function response and side effects to rapamycin for lymphangioleiomyomatosis: a prospective national cohort study
url https://eprints.nottingham.ac.uk/47947/
https://eprints.nottingham.ac.uk/47947/
https://eprints.nottingham.ac.uk/47947/