Health related quality of life in patients with idiopathic pulmonary fibrosis in clinical practice: insights-IPF registry

1Idiopathic pulmonary fibrosis (IPF) is a chronic, fibrosing interstitial lung disease associated with a high symptom burden, significant comorbidities and early death. Median survival is 3–5-years, shorter than for many malignancies. The antifibrotic drugs, pirfenidone and nintedanib, slow lung function decline but have not been convincingly shown to improve survival or quality of life (QoL). Beside prolonging survival, major aims for IPF therapy include improving symptoms and QoL domains like physical functioning, social participation and emotional well-being.

2A number of patient-reported outcome (PRO) measures have been used in IPF research. However, the majority of PRO data were generated in single-center cohorts or controlled clinical trials, and there are very limited QoL response data from IPF patients collected under real-world conditions. Such data could be used to improve understanding of disease burden at the individual and group levels, to better discern response to therapeutic interventions and to plan for trials of novel therapies.

3In the present study, we aimed to summarize QoL data collected in a nationwide, “real-world”, observational registry of patients with IPF and to examine associations between QoL and several other clinical variables.

4INSIGHTS-IPF (“Investigating significant health trends in idiopathic pulmonary fibrosis”) is an investigator-initiated, multicenter (19 centers from all parts of Germany), observational registry study of data collected, within the confines of routine clinical care, from patients with IPF since November 2012. The study materials were approved by the Ethics Committee of the Medical Faculty, Technical University of Dresden, and by further local ethic committees as per local requirements. INSIGHTS-IPF is registered at Clinicaltrials.gov (NCT01695408). The protocol and a detailed description of the baseline characteristics of the cohort have been previously published. In brief, patients are eligible for enrolment if they are at least 18 years old, have IPF (definite, probable or possible, applying the 2011 IPF guideline) based on physician diagnosis, and have provided written informed consent. There are no explicit exclusion criteria. Clinical data are collected at enrolment and thereafter at 6-month intervals. At follow-up visits, events such as hospitalization and acute exacerbation (as judged by the treating physician) are recorded. Data are reported via a secure internet based data collection form.

5Enrollees complete PROs at enrolment and yearly thereafter. PROs include the University of California San Diego Shortness of Breath Questionnaire (UCSD SOB), the St. George’s Respiratory Questionnaire (SGRQ), World Health Organization-5 Well-Being Index (WHO-5) and the EuroQol five-dimensional questionnaire (EQ-5D).

6This questionnaire includes 24 items, each with a response scale 0 (Not at all) to 5 (Maximally or Unable to do because of breathlessness). The total score ranges from 0 to 120, with a higher score indicating more severe dyspnea.

7The SGRQ was originally developed for patients with chronic obstructive pulmonary disease or asthma, however, as a respiratory disease-specific instrument, it has frequently been used in IPF. There are 50 items divided into three components (symptoms, activity, and impacts). Scores for each component and a total score range from 0 (highest QoL) to 100 (poorest QoL).

8The 5 items of the questionnaire tap mood, vitality, and general health. Each item is scored 0 to 5. The total ranges from 0 to 25, with higher scores connoting better well-being.

9The EQ-5D taps 5 domains (mobility, self-care, usual activities, pain or discomfort, and anxiety or depression) and is commonly used in cost-utility evaluation. Based on domain scores, a sum utility score is calculated ranging from negative values (−0.59 worse than death) to 1 (perfect state). Respondents also rate their current health on a 20-cm vertical visual analogue scale (VAS) scored from 0 to 100.

10Data were collected using an internet-based case report form (eCRF) with automated plausibility checks. On-site monitoring, with source data verification, was performed in the majority of centers (currently 70%).

11Summary statistics were generated for baseline data. Pearson product-moment correlation coefficients and univariate linear regression were used to examine associations between variables. Backward selection was used to generate multivariable models using the following candidate variable: disease duration, long-term oxygen therapy, physician’s judgment on IPF behavior (stable, slowly or rapidly progressing), NYHA stage, duration since first symptoms in years, GAP index, number and type of comorbidities (left heart insufficiency, coronary heart disease (CHD), carotid stenosis, stroke, peripheral arterial disease, atrial fibrillation, deep venous thrombosis (DVT), pulmonary arterial embolism, pulmonary hypertension, arterial hypertension, reflux, diabetes mellitus, emphysema, lung cancer, obstructive sleep apnea, depression/depressive disorder, anxiety), 6-min walk distance, gender, hospitalization in last 12 months, pulmonary rehabilitation, and CPI. Standard errors and confidence intervals were estimated by the Huber White sandwich estimator to account for the clustering of patients within the study centers. Data were analyzed with STATA 12.1 (StataCorp LP. Stata Statistical Software: Release 12. College Station, TX, USA).

12Data for QoL were available for 623 of a total of 737 patients (84.5%). Baseline characteristics are presented in Table 1. Patients mean age was 69.6 ± 8.7 years, 77.2% were male; all but one were Caucasian (99.7%). Their mean FVC was 67.5 ± 17.8% predicted and DLCO 35.6 ± 17% predicted. A comparison of baseline characteristics of the 623 patients with and 114 patients without available QoL data can be found in Additional file 1: Table S1.

13Patients were treated with antifibrotic therapies (49.5%), oral glucocorticoids (23.7%); N-acetylcysteine (33.7%), and long-term O2 therapy (32.3%). Most (90.0%) had definite IPF, 5% probable IPF, and 5% possible IPF. At enrolment, treating physicians rated IPF as stable in 36.3%, slowly progressing in 30.9% and rapidly progressing in 11.2%.

14Baseline values for PROs and their inter-correlations are shown in Table 2. According to the SGRQ, the greatest impairment was in the activity component. Based on the WHO-5 index, 46.4% of the patients showed depressive symptoms.

15For the SGRQ, associations with various demographic and clinical characteristics of patients at baseline are shown in Fig. 1. Statistically significantly higher total SGRQ score (indicating reduced QoL) were associated with lower age (51.8 for patients ≤60 years versus 46.9 for patients >65 years), female gender (46.9 for male versus 53 for female), higher NYHA classes (compared to NYHA class I), longer duration of symptoms, higher CPI, lower %FVC, and higher GAP stage (Fig. 1). Correlations between QoL and %DLCO (EQ-5D: 0.28, p < 0.001; SGRQ: -0.26, p < 0.001; UCSD: -0.22, p < 0.001) or %FVC (EQ-5D: 0.33, p < 0.001; SGRQ: -0.40, p < 0.001; UCSD: -0.43, p < 0.001) were moderately strong. Patients without comorbidity had a mean SGRQ total score of 44; those with 2 comorbidities 47; and those with ≥4 comorbidities 59 (ANOVA, p < 0.001 for difference between groups) (Table 3). QoL was also significantly associated with some types of pharmacological and non-pharmacological therapies of patients with IPF (Table 4).

16In multivariate models (Table 5), LTOT, GAP index (stage III), physician’s judgement (rapid progression), and NYHA class were independent predictors of EQ-5D VAS. The same variables (except for the GAP index) were associated with SGRQ total score.

17Both the EQ-5D index and the EQ-5D TTO were statistically significantly associated with LOT, the 6-MWD and the NYHA functional class (II, III, and IV). The WHO-5 was associated with LOT, and NYHA class III and IV. Finally, the UCSD SoB was associated with LOT, and NYHA class and %FVC.

18Idiopathic pulmonary fibrosis (IPF) is not only a severe life-shortening disease; it also significantly impairs patients’ quality of life. In this study, we present data from a large cohort of IPF patients. To our knowledge, this is one of the first-presentations of such data collected under real-world conditions. Overall, impairment in QoL and symptom burden were immense.

19Compared to a very recent report from the Australian IPF registry, QoL impairment was very similar with a SGRQ total score of 46.6 (and 48.3 in our registry). Similarly, to the data presented here, an association between QoL and dyspnoea and physiological data were reported. Yet, in contrast to our analyses also cough and depression were major contributors to diminished QoL – reasons for this may be explained by different tools used to assess depression (HADS) and a structured tool to assess cough severity. Another, yet retrospective very recently published cohort of 182 IPF patients reported an association between the SGRQ total score and overall survival. In comparison to recently-completed, randomised controlled drug trials, the patients in our registry had more severe QoL impairment and a higher symptom burden. For example, in the two INPULSIS trials of nintedanib, which together included 1066 patients, the mean total SGRQ score was 39.4–39.8 points in the various arms; it was 48.3 in our registry. The same is true of other drug trials for IPF: ambrisentan (492 subjects: mean SGRQ total 40.5–44.5), interferon gamma-1b (826 subjects: 41.6–42.4). Similarly, mean UCSD dyspnea score was higher in this registry (47.8) than participants in recently conducted trials (e.g., the ASCEND trial on pirfenidone, 555 patients, mean UCSD 34.0–36.6 points). Such differences in symptoms and QoL are likely explained by differences in disease severity and baseline characteristics. For example, in our real world cohort, the burden of comorbidities known to portend a worse prognosis in IPF was not insignificant, with 322 (51.7%) of our registry enrollees having at least two comorbid conditions. These patients would have been excluded from most drug trials.

20To our knowledge, this is the first time, investigators have assessed the association between the presence of specific comorbid conditions and QoL. We observed that comorbid conditions contribute greatly to QoL impairment. However, additional research is needed to determine if therapeutic targeting comorbidities will improve QoL in these patients. Although other investigators have assessed QoL in IPF patients under real-world conditions, they found no correlation between various baseline characteristics and QoL. This may stem from a lack of power. In our cohort, SGRQ total score was higher in women than men, an observation noted by other investigators. The reason for this difference is unknown but merits further investigation.

21Like other investigators, we found that QoL was more impaired in patients on LTOT than in those not on LTOT. In fact, LTOT was an independent predictor of QoL even with adjustment for disease severity. This likely stems from the real and perceived constraints LTOT places on patients. QoL impairment was also greater among patients who were prescribed anti-inflammatory therapy, anti-reflux therapy and other non-pharmacological interventions. In this observational study, causation cannot be discerned, and more research is needed to improve understanding of these results.

22In several studies, investigators reported correlation coefficients between the SGRQ and one or more other patient-related assessment of health related quality of life, health status or symptoms including the Borg Dyspnea Index, Cough Quality of Life Questionnaire, the Baseline Dyspnea Index, King’s Brief Interstitial Lung Disease questionnaire, Dyspnea Score, Short-Form 36 Physical Component Summary, Dyspnea-12, and UCSD SoB questionnaire among others. Overall, there were moderate to strong correlation between the SGRQ total score and the total score of these instruments, thus supporting the validity of the SGRQ total to capture QoL in patients with IPF. It is reassuring that data from our study mirror results from these other studies. Like them, our results support the validity of the SGRQ (and the other instruments used in INSIGHTS) for use in IPF, including a large, real-world, German cohort. In future research, shorter questionnaires with longitudinal and cross-cultural validity should be developed for use in daily patient care.

23In IPF patients, a major challenge is how to improve QoL impairment. Currently, only sildenafil, pulmonary rehabilitation or specialized, multi-modality treatment programs may have a role. Unfortunately, the two globally-approved anti-fibrotic drugs, nintedanib and pirfenidone, have not been shown to do so. Hopefully, ongoing development and research efforts will lead to therapeutic interventions that allow IPF patients to live better with the disease.

24There are limitations to our study. The QoL assessment tools we used were not originally developed for IPF, but they do have data to support their validity in this disease. Instruments such as the K-BILD or A Tool to Assess Quality of Life in Idiopathic Pulmonary Fibrosis (ATAQ-IPF-cA) which were developed for patients with interstitial lung disease may have reflected impairments more precisely in our cohort. However, these instruments’ psychometric properties have yet to be examined in German patients. Because all registry patients were being treated in specialized ILD centers, these results may not generalize to the larger IPF population. IPF was diagnosed at the participating centers according to current guidelines without undergoing another central MDT review which may explain some differences between the results reported here and clinical trial cohorts, although recent data suggest that experienced physicians are very accurate in diagnosing IPF. Further, QoL data may have been biased in the cohort reported here as incident IPF patients were slightly underrepresented compared to patients without available HrQoL data. However, a strength of the INSIGHTS-IPF registry is that enrollees were prospectively and consecutively recruited, and it employs source data verification, statistical plausibility checks and queries.

25Health related quality of life is substantially impaired in patients with IPF, and drivers of this impairment include symptoms, comorbidities, LOT and disease severity. While current treatments improve the course of the disease and perhaps survival, additional investigation is needed to identify interventions that durably to improve this important outcome in IPF patients.