Safety and Efficacy of Pirfenidone in Advanced Idiopathic Pulmonary Fibrosis: A Nationwide Post-Marketing Surveillance Study in Korean Patients.

AIM: The efficacy and safety of pirfenidone have been previously demonstrated in patients with mild-to-moderate idiopathic pulmonary fibrosis (IPF). However, the effect of pirfenidone in patients with advanced IPF remains unclear. Here, we investigated the effects of pirfenidone against advanced IPF in a real-world setting.
METHODS: A prospective nationwide post-marketing study was conducted on 258 patients from 10 Korean institutions. Patients with a predicted forced vital capacity (FVC) less than 50% or a diffusing capacity of the lung for carbon monoxide (DLco) less than 35% at baseline were classified as the advanced IPF group.
RESULTS: Of 219 patients included in the analysis, the majority were male (76.3%); the mean age was 67.3 years, and the advanced group accounted for 17.8% of the patients. The median treatment duration was 298 days. Among the subjects, 86.3% experienced adverse events (AEs), of which a decreased appetite (32.4%) and a photosensitivity reaction (13.7%) were the most frequent. The incidence of AEs was similar between the advanced and non-advanced groups (92.3% vs. 85.0%, respectively; p = 0.229). Although the overall discontinuation rate was higher in the advanced group than in the non-advanced group (74.4% vs. 50.0%, respectively; p = 0.006), the percentages of the patients who discontinued treatment as a result of AEs were similar in both groups (20.5% vs. 23.3%, respectively; p = 0.704). In all patients, the rates of decline in the predicted FVC and DLco over 48 weeks were - 4.3 ± 1.3% and - 4.4 ± 1.7%, respectively. There was no between-group difference in the rate of lung function decline.
CONCLUSIONS: Pirfenidone used for the treatment of patients with IPF in a real-world setting was well tolerated, with an acceptable safety profile and a consistent therapeutic effect, regardless of the disease severity. TRIAL REGISTRATION: ClinicalTrials.gov NCT03761082; the trial was retrospectively registered on December 3, 2018.

Key Summary Points

Introduction

Idiopathic pulmonary fibrosis (IPF) is a fatal fibrotic lung disease, associated with the worsening of dyspnea and a progressive decline in lung function, with a median patient survival of 2–5 years from diagnosis [1, 2]. Pirfenidone, an oral antifibrotic agent [3], was approved for IPF treatment in several countries, including Japan, European countries, and the USA. The drug has been commercially available in Korea since October 2012.

Previous clinical trials have shown that treatment of patients with IPF with pirfenidone attenuates lung function decline and reduces the risk of unexpected hospitalizations and mortality, with the drug showing an acceptable safety profile [4-9]. A post hoc analysis of pooled data from three phase 3 trials [10] also showed consistent benefits of pirfenidone for lung function in patients with IPF, regardless of the extent of lung function impairment [forced vital capacity (FVC) at least 80% vs. less than 80%] or the Gender–Age–Physiology stage (I vs. II–III). However, previous trials only included patients with mild-to-moderate IPF [predicted FVC at least 50% and predicted diffusing capacity of the lung for carbon monoxide (DLco) at least 35%], and thus, the effect of pirfenidone in patients with advanced IPF remains unclear.

Several real-world studies and post hoc analyses of the RECAP (NCT00662038) trial have suggested that pirfenidone may attenuate lung function decline in patients with advanced IPF [11-15]. However, these studies were mostly retrospective observational [11-15], single-center [11, 12], or descriptive studies [15]. Therefore, the aim of this study was to investigate the effect of pirfenidone treatment in patients with advanced IPF compared with that in patients with non-advanced IPF in a real-world setting.

Methods

Patients

Between 2014 and 2017, 258 patients with IPF were enrolled from 10 institutions in Korea and followed up until treatment discontinuation or the end of the study period. The diagnosis of IPF was confirmed through multidisciplinary discussion at each site, based on the American Thoracic Society (ATS)/European Respiratory Society (ERS)/Japanese Respiratory Society/Latin American Thoracic Association guidelines [1]. According to the package insert statement, an initial dose of 200 mg of pirfenidone was administered three times daily with meals (600 mg/day). Thereafter, the dose was gradually increased by 200 mg every 2 weeks to a maximum of 600 mg per dose (1800 mg/day). The study protocol was approved by the institutional review board of each institution, and the study was performed in accordance with the principles of the Helsinki Declaration of 1964 and its later amendments, as well as any relevant regulatory requirements. All patients provided written informed consent. Patients with a predicted FVC less than 50% or DLco less than 35% at baseline were classified as the advanced group.

Data Collection

Lung function (FVC and DLco) and subjective symptoms (dyspnea and cough) were assessed at 12-week intervals (i.e., 0, 12, 24, 36, and 48 weeks). Spirometry and DLco measurements were performed on the basis of the ERS/ATS guidelines, and the results were presented as percentages of normal predicted values [16-18]. Dyspnea was assessed on a scale of 1 to 5, according to the British Medical Research Council, and the severity of cough was classified into four grades (none, mild, moderate, and severe) [19].

Evaluation of Safety and Efficacy

Safety was evaluated in patients who received pirfenidone at least once and were followed up for safety assessment. Treatment-emergent events were defined as outcomes that occurred from the first dose of pirfenidone until 7 days after discontinuation. Adverse events (AEs) were reported using preferred terms according to the Medical Dictionary for Regulatory Activities, version 21.0. Acute exacerbations of IPF were reported by investigators and were defined as events meeting all of the following criteria: (1) worsening of dyspnea within a 1-month period; (2) newly developed pulmonary infiltrates, observed on chest computed tomography images; (3) reduction of arterial oxygen tension (a decrease of at least 10 mmHg in partial oxygen pressure compared with stable pressure); and (4) no evidence of precipitating factors such as infection or heart disease [4, 5].

Efficacy was evaluated in patients who were treated for at least 12 weeks and underwent lung function tests before and after treatment. The rate of lung function decline and absolute mean changes in predicted FVC% and DLco% values from baseline to 48 weeks were analyzed using the mixed-effects model repeated measurement (MMRM) to minimize the influence of missing data on calculated lung function [20, 21]. Disease progression was determined as the absolute decline of the predicted FVC at least 10% or DLco at least 15% [1, 22]. Categorized changes in dyspnea and cough were defined as improved (decreased score), stable (no change), or worsened (increased score). Progression-free survival (PFS) was defined as the time from treatment initiation to the first occurrence of disease progression or death.

Statistical Analysis

Data are expressed as the mean ± standard deviation, the mean ± standard error (SE), or numbers with percentages, as appropriate. An independent t test or Wilcoxon’s rank-sum test was used for comparison of continuous variables between the groups, and Fisher’s exact test or Pearson’s chi-squared test was used for comparison of categorical variables between the groups. MMRM was used to analyze the rate of lung function decline and the absolute mean changes of FVC and DLco from baseline (fixed variables: visit, age, sex, and smoking status; random effect: participant’s identification number). The results (rate of lung function decline and absolute mean changes from baseline) for the advanced and non-advanced groups were compared using group and group-by-visit as fixed effects, in addition to MMRM. The event-free probability was estimated using the Kaplan–Meier method, and a log-rank test was used for assessing differences between the two groups. Adjusted hazard ratios (aHRs) and 95% confidence intervals (CIs) were generated using Cox’s proportional hazards model adjusted for age and sex. All statistical analyses were performed using SAS (version 9.4, SAS Institute, Cary, NC, USA). A two-sided p value less than 0.05 indicated significant differences.

Results

Baseline Characteristics

Of the 258 enrolled patients, 39 were excluded from the analysis because of off-label drug use (n = 13) or missing baseline lung function data (n = 26). Therefore, safety was evaluated in 219 patients (39 in the advanced group and 180 in the non-advanced group) (Fig. 1). The baseline characteristics of patients are provided in Table 1 and in Table S1 in the supplementary material. The patients were mostly male (76.3%) and ever-smokers (68.9%), and the mean age was 67.3 years. The median time since diagnosis was 1.0 year (advanced 1.5 years vs. non-advanced 0.9 years). The median duration of treatment was 298 days, with 64.4% of the patients treated for at least 180 days. Compared with the patients in the non-advanced group, those in the advanced group had more severe subjective symptoms (cough and dyspnea), lower lung function, and more frequently received immunosuppressants at baseline. Pulmonary hypertension tended to be more prevalent in the advanced group than in the non-advanced group (5.1% vs. 0.6%, respectively; p = 0.083). However, there were no between-group differences in other comorbidities.

Fig. 1

Patient disposition

Table 1

Baseline characteristics of the patients in the advanced and non-advanced IPF groups

Characteristic	Total	Advanced	Non-advanced	p value
Patients, n	219	39	180
Male sex	167 (76.3)	30 (76.9)	137 (76.1)	0.914
Ever-smoker	151 (68.9)	27 (69.2)	124 (68.9)	0.967
Age, years	67.3 ± 8.0	65.3 ± 9.3	67.7 ± 7.7	0.161
Time since diagnosis, years, median (Q1, Q3)	1.0 (0.1, 3.1)	1.5 (0.3, 3.7)	0.9 (0.1, 2.8)	0.110
Treatment duration, days, median (Q1, Q3)	298 (114, 365)	212 (96, 344)	320 (116, 367)	0.212
Follow-up duration, days, median (Q1, Q3)	322 (127, 370)	212 (96, 349)	329 (131, 372)	0.176
Daily dose, mg	1081.6 ± 430.4	1110.3 ± 422.6	1075.4 ± 432.9	0.773
FVC, % predicted	65.0 ± 15.3	46.4 ± 10.7	69.0 ± 13.0	< 0.001
DLco, % predicted	52.3 ± 16.2	35.0 ± 11.1	56.0 ± 14.6	< 0.001
IPF treatment at baseline
Steroid	7 (3.2)	3 (7.7)	4 (2.2)	0.553
Immunosuppressant	2 (0.9)	2 (5.1)	0 (0.0)	0.031
Cysteine derivative	25 (11.4)	3 (7.7)	22 (12.2)	0.582
Oxygen therapy at baseline	5 (2.3)	2 (5.1)	3 (1.7)	0.217
Comorbidities	178 (81.3)	34 (87.2)	144 (80.0)	0.297
Hypertension	60 (27.4)	12 (30.8)	48 (26.7)	0.603
Diabetes mellitus	60 (27.4)	12 (30.8)	48 (26.7)	0.603
GERD	33 (15.1)	6 (15.4)	27 (15.0)	0.952
Hyperlipidemia	25 (11.4)	5 (12.8)	20 (11.1)	0.782
Emphysema	8 (3.7)	2 (5.1)	6 (3.3)	0.635
COPD	6 (2.7)	1 (2.6)	5 (2.8)	1.000
Pulmonary hypertension	3 (1.7)	2 (5.1)	1 (0.6)	0.083

Data are presented as the mean ± standard deviation or number (%), unless otherwise specified

Q1 quartile 1 (25th percentile), Q3 quartile 3 (75th percentile), GERD gastroesophageal reflux disease, COPD chronic obstructive pulmonary disease, IPF idiopathic pulmonary fibrosis, FVC forced vital capacity, DLco diffusing capacity of the lung for carbon monoxide

Adverse Events

A total of 86.3% of the patients experienced AEs, of which a decreased appetite (32.4%) and a photosensitivity reaction (13.7%) were the most frequent ones (Table 2). The incidence of AEs was similar in the advanced and non-advanced groups (92.3% vs. 85.0%, respectively; p = 0.229; Table 2). The time-to-event analysis showed that most AEs occurred during the first 24 weeks of treatment; the Kaplan–Meier estimate of event-free probability at week 24 was 20.0% (95% CI 14.8–25.8%; Fig. S1 in the supplementary material). The probability of having any AEs was higher in the advanced group than in the non-advanced group (median time 6.4 vs. 9.0 weeks, respectively; aHR 1.6; 95% CI 1.1–2.3; p = 0.020; Fig. S1 in the supplementary material and Fig. 2). Similarly, dyspnea (incidence 18.0% vs. 6.1%, respectively; aHR 3.4; 95% CI 1.3–8.9; p = 0.012) and progression of IPF (incidence 15.4% vs. 5.6%, respectively; aHR 3.1; 95% CI 1.1–8.6; p = 0.030) were more prevalent in the advanced group than in the non-advanced group. However, there was no between-group difference in the risk of gastrointestinal (decreased appetite, nausea, epigastric discomfort, constipation, dyspepsia, and diarrhea) and skin-related events (photosensitivity reaction, rash, and pruritus) (Fig. 2). Serious AEs (SAEs) occurred more frequently in the advanced group than in the non-advanced group (30.8% vs. 15.0%, respectively; p = 0.020). The most common SAEs were progression of IPF in the advanced group and pneumonia in the non-advanced group (Table 2).

Table 2

Adverse events (frequency at least 3%) in the advanced and non-advanced IPF groups

Characteristic	Total	Advanced	Non-advanced	p value
Patients, n	219	39	180
Adverse events	189 (86.3)	36 (92.3)	153 (85.0)	0.229
Decreased appetite	71 (32.4)	13 (33.3)	58 (32.2)	0.893
Photosensitivity reaction	30 (13.7)	6 (15.4)	24 (13.3)	0.736
Rash	25 (11.4)	2 (5.1)	23 (12.8)	0.266
Nausea	24 (11.0)	6 (15.4)	18 (10.0)	0.394
Pruritus	24 (11.0)	1 (2.6)	23 (12.8)	0.087
Epigastric discomfort	22 (10.1)	4 (10.3)	18 (10.0)	1.000
Cough	21 (9.6)	2 (5.1)	19 (10.6)	0.383
Pneumonia	19 (8.7)	6 (15.4)	13 (7.2)	0.117
Dyspnea	18 (8.2)	7 (18.0)	11 (6.1)	0.023
Progression of IPFa	16 (7.3)	6 (15.4)	10 (5.6)	0.044
Productive cough	15 (6.9)	4 (10.3)	11 (6.1)	0.314
Constipation	13 (5.9)	3 (7.7)	10 (5.6)	0.707
Fatigue	11 (5.0)	4 (10.3)	7 (3.9)	0.111
Asthenia	10 (4.6)	1 (2.6)	9 (5.0)	1.000
Dizziness	10 (4.6)	1 (2.6)	10 (5.6)	0.694
Upper respiratory tract infection	9 (4.1)	0 (0.0)	9 (5.0)	0.367
Dyspepsia	8 (3.7)	2 (5.1)	6 (3.3)	0.635
Diarrhea	8 (3.7)	2 (5.1)	6 (3.3)	0.635
Abnormal liver function test	8 (3.7)	1 (2.6)	7 (3.9)	1.000
Serious adverse eventsb	39 (17.8)	12 (30.8)	27 (15.0)	0.020
Pneumonia	15 (6.9)	3 (7.7)	12 (6.7)	0.734
Progression of IPFc	13 (5.9)	4 (10.3)	9 (5.0)	0.255
Adverse drug reactionsd	151 (69.0)	27 (69.2)	124 (68.9)	0.967

Data are presented as the number (%), unless otherwise specified

IPF idiopathic pulmonary fibrosis

aIncludes acute exacerbations of IPF (n = 9)

bA serious adverse event was defined as an adverse event that was fatal or life-threatening, required prolonged hospitalization, was associated with a congenital anomaly, or was deemed to be serious for any other reason

cThese were the events meeting one of the criteria for serious adverse events among the adverse events of progression of IPF

dA summary of adverse drug reactions with a frequency of at least 3% is presented in Table S5 in the supplementary material

Fig. 2

Forest plot demonstrating treatment-emergent adverse events and progression-free survival in the advanced and non-advanced IPF groups. Hazard ratios between the advanced and non-advanced groups were compared using Cox’s proportional hazards model adjusted for age and sex. IPF idiopathic pulmonary fibrosis, CI confidence interval. aIncluded decreased appetite, nausea, epigastric discomfort, constipation, dyspepsia, and diarrhea; bIncluded photosensitivity reaction, rash, and pruritus; cIncluded exacerbations and acute exacerbations of IPF; dProgression-free survival was defined as the time from treatment initiation to the occurrence of death or disease progression (determined as an absolute decline of the predicted FVC at least 10% or DLco at least 15%)

Disease-Related AEs

Event rates for investigator-reported acute exacerbation, death, and hospitalization are summarized in Table S2 in the supplementary material. Investigator-reported acute exacerbation occurred in 4.1% (n = 9) of all patients, and no between-group difference was observed (advanced group 7.7% vs. non-advanced group: 3.3%; p = 0.202). The rate of death from all causes and from IPF was 5.9% (n = 13) and 3.2% (n = 7), respectively. The time-to-event analysis showed a higher risk of all-cause deaths in the advanced group than in the non-advanced group (incidence 15.4% vs. 3.9%, respectively; aHR 4.4; 95% CI 1.5–13.1; p = 0.008), but there was no significant between-group difference in the risk of IPF-related deaths (incidence 7.7% vs. 2.2%, respectively; aHR 3.8; 95% CI 0.9–16.9; p = 0.082; Fig. 2 and Table S2 in the supplementary material).

All-cause hospitalization was reported in 15.1% of all patients (n = 33), mainly as a result of respiratory-related reasons such as pneumonia and progression of IPF. There was no significant difference in the risk of all-cause hospitalization between groups (incidence 20.5% vs. 13.9%; aHR 1.9; 95% CI 0.9–4.3; p = 0.108). However, the advanced group showed a greater risk of respiratory hospitalization than did the non-advanced group (incidence 20.5% vs. 11.1%, respectively; aHR 2.5; 95% CI 1.1–5.8; p = 0.031; Fig. 2 and Table S2 in the supplementary material). There was no significant difference in progression-free survival between the groups (aHR 1.4; 95% CI 0.7–2.8; p = 0.381; Fig. 2).

Treatment Discontinuation

Treatment was prematurely discontinued in 54.3% of the patients (Table 3). The advanced group had a higher rate of discontinuation than did the non-advanced group (74.4% vs. 50.0%, respectively; p = 0.006). The most common reason for discontinuation was AEs (22.8%), followed by patient request (16.0%), no revisit (9.1%), progression of IPF (5.0%), and insufficient efficacy (1.4%). There were no between-group differences in the reasons for discontinuation, except progression of IPF (advanced group 12.8% vs. non-advanced group 3.3%; p = 0.028). Of 189 patients who experienced AEs, 55.6% continued treatment without dose interruption, and no between-group difference was observed (Table S3 in the supplementary material).

Table 3

Reasons for premature discontinuation of the treatment in the advanced and non-advanced IPF groups

Reasons for discontinuation	Total	Advanced	Non-advanced	p value
Total patients, n	219	39	180
Discontinued patients	119 (54.3)	29 (74.4)	90 (50.0)	0.006
Adverse event	50 (22.8)	8 (20.5)	42 (23.3)	0.704
Decreased appetite	10 (4.6)	1 (2.6)	9 (5.0)	1.000
Photosensitivity reaction	9 (4.1)	1 (2.6)	8 (4.4)	1.000
Rash	6 (2.7)	0 (0.0)	6 (3.3)	0.594
Cough	4 (1.8)	0 (0.0)	4 (2.2)	1.000
Dyspnea	4 (1.8)	1 (2.6)	3 (1.7)	0.546
Epigastric discomfort	4 (1.8)	1 (2.6)	3 (1.7)	0.546
Nausea	4 (1.8)	0 (0.0)	4 (2.2)	1.000
Pneumonia	4 (1.8)	0 (0.0)	4 (2.2)	1.000
Abdominal pain	2 (0.9)	0 (0.0)	2 (1.1)	1.000
Dizziness	2 (0.9)	0 (0.0)	2 (1.1)	1.000
Myocardial infarction	2 (0.9)	1 (2.6)	1 (0.6)	0.325
Pruritus	2 (0.9)	0 (0.0)	2 (1.1)	1.000
Pyrexia	2 (0.9)	1 (2.6)	1 (0.6)	0.325
Patient requesta	35 (16.0)	10 (25.6)	25 (13.9)	0.069
Before October 2, 2015	28 (12.8)	8 (20.5)	20 (11.1)	0.118
After October 2, 2015	7 (3.2)	2 (5.1)	5 (2.8)	0.611
No revisit	20 (9.1)	5 (12.8)	15 (8.3)	0.365
Progression of IPFb	11 (5.0)	5 (12.8)	6 (3.3)	0.028
Insufficient efficacy	3 (1.4)	1 (2.6)	2 (1.1)	0.446

Data are presented as the number (%), unless otherwise specified

IPF idiopathic pulmonary fibrosis

aThe medication cost was not covered by the National Health Insurance Service in Korea until October 2015

bIncludes acute exacerbations of IPF (n = 6)

Changes in Lung Function

Changes in lung function from baseline to 48 weeks were evaluated in 137 patients (19 in the advanced group and 118 in the non-advanced group). The patients were mostly male (74.5%) and ever-smokers (70.1%), with a median treatment duration of 346 days (range 99–889 days). The baseline characteristics were comparable between the groups, except for lung function (Table S4 in the supplementary material). The adjusted absolute change (± SE) from baseline to 48 weeks in the predicted FVC was − 3.1 ± 0.8%, and that in the predicted DLco was − 5.0 ± 1.2% (Fig. 3a, b). The adjusted decline rate over 48 weeks in the predicted FVC was − 4.3 ± 1.3%, and that in the predicted DLco was − 4.4 ± 1.7% (Fig. 3c, d). Overall, no between-group differences were observed in the mean FVC and DLco changes and in the adjusted rates of lung function decline, which indicated a consistent treatment effect, irrespective of disease severity. The proportion of patients who experienced an FVC decline of at least 10% or a DLco decline of at least 15% was 13.1% and 14.6%, respectively. No significant differences were observed in terms of categorical changes in lung function between the groups (Fig. S2a, b in the supplementary material).

Fig. 3

Comparison of absolute changes and annual decline rates in the predicted FVC% and DLco%. a Adjusted mean absolute change in the predicted FVC%. b Adjusted mean absolute change in the predicted DLco%. c Adjusted decline rate of FVC (% predicted/48 weeks). d Adjusted decline rate of DLco (% predicted/48 weeks). Values are the mean ± SE. The mixed-effects model repeated measurement (MMRM) was used to analyze the rate of decline of lung function and the mean changes of FVC and DLco from baseline, with the visit, age, sex, and smoking status as fixed effects and participant’s identification number as the random effect. To compare the results between the advanced and non-advanced groups, the group and the group-by-visit were used as a fixed effect, in addition to MMRM. FVC forced vital capacity, DLco diffusing capacity of the lung for carbon monoxide

Changes in Subjective Symptoms

Of 160 patients (26 in the advanced group and 134 in the non-advanced group) who were treated for at least 12 weeks and whose subjective symptoms were assessed before and after treatment, 8.8% experienced improvement, 70.6% experienced stabilization, and 20.6% experienced a worsening of dyspnea (Fig. S2c in the supplementary material). The proportion of patients with improved, stable, and worsened cough was 11.9%, 68.8%, and 19.4%, respectively (Fig. S2d in the supplementary material). There were no significant between-group differences in categorical changes of the subjective symptoms.

Discussion

This was the first nationwide study conducted to obtain prospective real-world data on the treatment effect of pirfenidone in Korean patients with IPF. We conducted a post hoc analysis of the data collected to compare the therapeutic effects of pirfenidone in patients with advanced IPF and in those with non-advanced IPF. Our study demonstrated that pirfenidone had an acceptable safety profile and showed a consistent efficacy in terms of stabilizing lung function and subjective symptoms, regardless of IPF disease severity.

The types of AEs observed were similar in the advanced and non-advanced IPF groups and were consistent with the known safety profile of pirfenidone. Most AEs occurred within the first 6 months of treatment, and the frequency of AEs was reduced over time. The multivariate Cox analysis showed that the advanced group had a greater risk of experiencing AEs than did the non-advanced group. This difference appeared to be due to an increased risk of progression of IPF and dyspnea in the advanced group, which could be attributed to the severity of the disease. However, there was no significant difference in the risk of drug-related gastrointestinal and skin-related events between the groups. Most AEs were mild or moderate in severity and reversible upon treatment interruption. The treatment discontinuation rate was higher in the advanced group than in the non-advanced group, similar to previous studies [15, 23, 24]. However, the proportion of patients who discontinued treatment as a result of AEs (22.8%) was similar in both groups and was not different from that reported in other observational studies (18.4–26.7%) [11–15, 24]. In this study, the rate of discontinuation by patient request (16.0%) was relatively higher than that reported in a Japanese post-marketing study (5.3%) [24], but our finding should be interpreted with caution because the medication cost was not covered by the National Health Insurance Service in Korea until October 2015. Importantly, 12.8% of all patients discontinued treatment because of economic reasons before October 2015; however, the rate of discontinuation decreased (3.2%) thereafter.

Acute exacerbation of IPF is a common and fatal complication, especially in patients with progressive disease, with a 1-year incidence of 5–14.2% [25, 26]. In our study, the incidence of acute exacerbation was lower (4.1%) than that reported in previous studies [25, 26], and there was no significant difference in the risk of acute exacerbations between the advanced and non-advanced groups (Fig. S3 in the supplementary material). It has been reported that patients with lower lung function are at a greater risk of acute exacerbation of IPF [25]. Collectively, our study results suggest that pirfenidone treatment might be more beneficial in preventing acute exacerbation in patients with advanced IPF who are at a higher risk of such an event than in those with non-advanced IPF. A post hoc analysis of ASCEND (NCT01366209) and CAPACITY trials (NCT00287716 and NCT00287729) also showed a significantly lower risk of respiratory hospitalization in patients with advanced IPF (predicted FVC less than 50% or DLCO less than 30%) than placebo-treated patients (HR 0.4; 95% CI 0.2–0.9; p = 0.021); IPF was the most frequent reason for respiratory hospitalization [27].

It has been reported that acute respiratory events, which are mostly caused by acute exacerbation and pulmonary infections, are common in patients with IPF and lead to hospitalization [25], which is associated with a decreased survival of patients with IPF [9, 28, 29]. In this study, of the patients who died during the study (n = 13), approximately half (46.2%, n = 6) underwent respiratory hospitalization, and the advanced group showed a greater risk of respiratory hospitalization, mainly due to pneumonia and progression of IPF.

The baseline disease severity, the time since diagnosis, and the presence of comorbidities have been associated with a decreased survival of patients with IPF [30, 31]. In our study, while the rate of all-cause deaths was higher in the advanced group than in the non-advanced group (15.4% vs. 3.9%, respectively; p = 0.014), no significant between-group difference was observed in the rates of IPF-related deaths (7.7% vs. 2.2%, respectively; p = 0.109). Non-IPF-related deaths frequently occurred in the population of patients with IPF, the majority of which are elderly people [2]; therefore, IPF-related deaths could be a more accurate measure of the treatment efficacy. Thus, our results may provide more accurate evidence of the clinical benefit of pirfenidone in patients with advanced IPF; however, the number of patients was too small for conclusions to be drawn.

The absolute decline and annual decline rate in FVC in patients with advanced IPF were comparable to those in patients with non-advanced IPF; a similar trend was observed for DLco. The rates of disease progression, subjective symptoms, and PFS were also similar between the groups. These results suggested that pirfenidone-treated patients with advanced IPF might experience a similar degree of efficacy as that in patients with non-advanced IPF. Similar findings were also reported in recent studies [11–15, 23]. Post hoc analyses of the RECAP trial reported that the rate of the annual FVC decline in patients with advanced IPF (predicted FVC less than 50% or DLco less than 35%) was similar to that in patients with less advanced IPF (3.8% vs. 3.9%, respectively) [15]. In the INPULSIS-ON study, in which patients were treated with nintedanib, the absolute changes in FVC from baseline to week 48 were similar in patients with predicted FVC values at most 50% and greater than 50% (− 62.3 vs. − 87.9 mL, respectively) [23]. A retrospective study of pirfenidone including 43 patients with severe IPF (predicted FVC less than 50% or DLco less than 35%) conducted by Tzouvelekis et al. [14] also showed that the rate of FVC decline at 6 months of treatment was not significantly different between groups with predicted FVC less than 50% and at least 50% (4.7 ± 8.9 vs. − 0.6 ± 11.8%, respectively; p = 0.2).

There are several limitations to this study. First, the number of patients in the advanced group was smaller than that in the non-advanced group. In order to overcome this limitation, we analyzed the data from various perspectives, and our study showed consistent trends in the treatment effects across different parameters such as lung function change, subjective symptoms change, hospitalization, mortality, and progression-free survival between the two groups, with the results being highly consistent with those of previous studies. Second, the absence of a control group limited the extent of a meaningful interpretation of the results. However, previous randomized, placebo-controlled trials have demonstrated that pirfenidone treatment shows sufficient effects in patients with IPF. Third, the IPF diagnosis was performed by participating investigators, which could have led to a confirmation bias in some patients. However, the demographic and clinical features were comparable to those of other studies. Fourth, it should be also recognized that the results of this study are limited by the relatively lower dosage used (at most 1800 mg/day), and the minimum treatment duration of 12 weeks for efficacy evaluation. However, considering the standard body weight in Korea, the weight-adjusted dose in this study could be comparable to that in European countries and the USA. In addition, a significant treatment effect of pirfenidone versus placebo was evident from week 12 in CAPACITY phase 3 trials. Lastly, a relatively high proportion of patients discontinued treatment as a result of reimbursement restrictions. As a result, the treatment discontinuation may have been overestimated.

Conclusions

The results of this study indicated that treatment with pirfenidone in a real-world setting produced an acceptable safety profile and a consistent therapeutic effect in patients with IPF in terms of stabilizing lung function and subjective symptoms, regardless of the disease severity. Additional studies may be needed to further confirm these findings.

Below is the link to the electronic supplementary material.

Supplementary file1 (DOC 1628 kb)

Why carry out this study?

The efficacy and safety of pirfenidone have been previously demonstrated in patients with mild-to-moderate idiopathic pulmonary fibrosis (IPF), but the effect of pirfenidone in patients with advanced IPF remains unclear.

Several real-world studies have suggested that pirfenidone may attenuate lung function decline in patients with advanced IPF, but these studies were mostly retrospective observational, single-center, or descriptive studies.

We investigated the effects of pirfenidone against advanced IPF in a real-world setting.

What was learned from the study?

Treatment with pirfenidone in a real-world setting produced an acceptable safety profile and a consistent therapeutic effect in patients with IPF in terms of stabilizing lung function and subjective symptoms, regardless of the disease severity.

Although the demographic and clinical features of the present study were comparable to those of other studies, additional studies may be needed to further confirm these findings.