Chest · 2026
Impact of Antifibrotic Adherence and Dosing on Risk of Mortality and Hospitalization in Idiopathic Pulmonary Fibrosis: A Nested Case-Control Study.
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Xu Huiping, Meier Erin, Chhabria Mamta S, DeDent Alison M, Hui Siu L, Zhang Zuoyi, Boente Ryan D
Аннотация
BACKGROUND: Antifibrotics, including nintedanib and pirfenidone, are effective in slowing the decline of lung function for patients with idiopathic pulmonary fibrosis (IPF). However, their adoption rates are remarkably low, and substantial proportions of patients undergo dose reduction or treatment discontinuation because of the high incidence of adverse events.
RESEARCH QUESTION: What is the impact of treatment modification on all-cause mortality and hospitalization?
STUDY DESIGN AND METHODS: Using a large administrative database, patients with IPF were identified who initiated antifibrotic treatment. A nested case-control design was used to match cases and controls at a 1:1 ratio, and conditional logistic regression was performed to estimate the effect of antifibrotic adherence and dosing. Adherence was measured by using the proportion of days covered. Both adherence and dosing were determined based on the exposure period between antifibrotic initiation (cohort entry date) and outcome occurrence (index date).
RESULTS: Adherence (proportion of days covered ≥ 0.75) was associated with lower risk of mortality (odds ratio, 0.563; P < .001), regardless of which antifibrotic was used. Patients taking a reduced dose had a significantly greater risk of mortality compared with those taking the standard dose (OR, 1.57; P = .024), but this was only observed in those who started nintedanib. For hospitalization, adherence was associated with a lower risk (OR, 0.692; P = .016) overall, and reduced doses were associated with a higher risk (OR, 1.667; P = .008) only among patients who started nintedanib. Among patients who started pirfenidone, neither adherence nor dose was associated with the risk of hospitalization.
INTERPRETATION: The results of this study suggest that antifibrotic adherence and dosing are important factors that influence mortality and hospitalization. A multidisciplinary approach involving nutritionists, drug clinical educators, and other key stakeholders to facilitate early access, affordable treatment, and adverse event mitigation may enhance adherence and ultimately improve patient outcomes.
RESEARCH QUESTION: What is the impact of treatment modification on all-cause mortality and hospitalization?
STUDY DESIGN AND METHODS: Using a large administrative database, patients with IPF were identified who initiated antifibrotic treatment. A nested case-control design was used to match cases and controls at a 1:1 ratio, and conditional logistic regression was performed to estimate the effect of antifibrotic adherence and dosing. Adherence was measured by using the proportion of days covered. Both adherence and dosing were determined based on the exposure period between antifibrotic initiation (cohort entry date) and outcome occurrence (index date).
RESULTS: Adherence (proportion of days covered ≥ 0.75) was associated with lower risk of mortality (odds ratio, 0.563; P < .001), regardless of which antifibrotic was used. Patients taking a reduced dose had a significantly greater risk of mortality compared with those taking the standard dose (OR, 1.57; P = .024), but this was only observed in those who started nintedanib. For hospitalization, adherence was associated with a lower risk (OR, 0.692; P = .016) overall, and reduced doses were associated with a higher risk (OR, 1.667; P = .008) only among patients who started nintedanib. Among patients who started pirfenidone, neither adherence nor dose was associated with the risk of hospitalization.
INTERPRETATION: The results of this study suggest that antifibrotic adherence and dosing are important factors that influence mortality and hospitalization. A multidisciplinary approach involving nutritionists, drug clinical educators, and other key stakeholders to facilitate early access, affordable treatment, and adverse event mitigation may enhance adherence and ultimately improve patient outcomes.