Effect of pirfenidone on lung function decline and survival: 5-yr experience from a real-life IPF cohort from the Czech EMPIRE registry

Idiopathic pulmonary fibrosis (IPF) belongs to the idiopathic interstitial pneumonias; it is characterised by a progressively declining lung function, leading to respiratory failure and death, with a median survival of 2–3 years following initial diagnosis [1, 2]. Epidemiological data in many countries are likely underestimated as the diagnosis of IPF tends to be mistaken or missed completely [3] thus an extensive need to establish national and international registries occurred. The Czech IPF registry was launched in June 2012, and on its basis the EMPIRE (European MultiPartner IPF Registry) project was launched in 2014 aiming at the assessment of IPF incidence, prevalence, and mortality in Central and Eastern Europe, the determination of basic patients’ characteristics and used treatment (http://empire.registry.cz/index-en.php).

Since 2015, antifibrotic therapy with either pirfenidone or nintedanib has been recommended in IPF patients [2, 4]. Although the treatment with pirfenidone is not curative, the clinical trials showed that it reduces disease progression, as reflected by lung function, exercise tolerance, and progression-free survival [5–7] and improves life expectancy [8]. There is a growing body of evidence that early diagnosis and early initiation of treatment by pirfenidone may preserve lung functional status and prolong life. A positive effect of pirfenidone on disease progression was also recently observed in patients with more advanced disease with less preserved lung function [9–12].

The effectiveness of pirfenidone in terms of reduced forced vital capacity (FVC) decline, decline in 6-min’ walk test distance (6-MWT) and increase of progression-free survival at 12 months after administration has been proven in Phase III CAPACITY/ASCEND population [7, 8] and cohorts from Belgium and the Netherlands [13], Italy [11], Japan [14], Germany [15], the UK [16], Sweden [17], Denmark [18], and Greece [12]. However, long-term data on disease progression in IPF patients treated with pirfenidone is still limited [19, 20].

We therefore investigated 2- and 5-yrs overall survival and lung function declination in IPF patients during long-term treatment with i) pirfenidone and ii) no-antifibrotic drugs. Additionally, the relationship between lung function declination and mortality was estimated. Data was collected prospectively from IPF patients enrolled in the Czech IPF registry between December 2012 to December 2017 in a real-life approach.

In this study, IPF patients (n = 841) from the Czech IPF registry, a national registry within an international multicentre database of patients with IPF in Central and Eastern Europe (EMPIRE, European MultiPartner IPF Registry) were enrolled (Fig. 1). All patients were diagnosed according to the American Thoracic Society (ATS)/European Respiratory Society (ERS) consensus classification [1] in 15 centres for interstitial lung diseases (ILDs) in the Czech Republic between December 2012 to December 2017. The complete clinical and demographical data (age, gender, treatment start, type of treatment, lung function before and during treatment, comorbidities) were available in 601 patients. 240 patients (28.5%) were excluded from further analysis due to a change of diagnosis (n = 6), unknown type of treatment or unknown date of treatment start (n = 89) or nintedanib treatment (n = 145). Of those with complete clinical and demographical data, 383 (63.7%) patients were treated with pirfenidone and 218 (36.3%) patients treated with other modalities (corticosteroids, N-acethylcystein (NAC), azathioprine and their combinations). Patient demographic and clinical characteristics are shown in Table 1. The assessment of forced vital capacity (FVC) and diffusing lung capacity for carbon monoxide (DL_CO) and mortality in enrolled patients were investigated at treatment initiation (max 1 month to treatment start) with 6 (±1), 12 (±1), 18 (±2), and 24 (±2) months follow-up. Disease progression as measured by FVC decline was considered at two values (≥5%, ≥10%) and/or by DL_CO decline at two values (≥10%, ≥15%) [21–23]. Patients on nintedanib were not included in this study because this drug was commercially available in the Czech Republic after September 2016, and most patients on this treatment were followed for less than one year at the end of this study.

Number of patients (%)	Total	Pirfenidone treatment	No-antifibrotic treatment	P-value (pirfenidone vs no-antifibrotics)
Patients, %	601 (100.0%)	383 (63.7%)	218 (36.3%)
Gender (male/female), number (%)	431 (71.7%)/170 (28.3%)	281 (73.4%)/102 (26.6%)	150 (68.8%)/68 (31.2%)	0.258
Age (< 60/60–69/> 70 yrs)	106/236/259	66/157/160	40/79/99	0.520
Smoking status				0.057
Non smokers	275 (45.8%)	166 (43.3%)	109 (50.0%)
Exsmokers	316 (52.6%)	213 (55.6%)	103 (47.2%)
Smokers	10 (1.7%)	4 (1.0%)	6 (2.8%)
FVC (%), predicted, at the treatment initiation Mean ± SD	71.7 ± 15.9	70.7 ± 13.2	74.2 ± 20.8	0.068
DLCO (%), predicted, at the treatment initiation Mean ± SD	46.1 ± 13.6	47.8 ± 12.1	41.9 ± 16.1	< 0.001
FVC ≥50% and ≤ 90% predicted & DLCO ≥ 35%, yes/no, number (%)	432/169 (71.9%/28.1%)	322/61 (84.1%/15.9%)	110/108 (50.5%/49.5%)	< 0.001

In July 2012, the first Czech patients with IPF were selected for pirfenidone therapy in the frame of The European Named Patient Programme (InterImmune International AG) and continued from July 2014 with a commercially available drug. The Czech guidelines for treatment of IPF from 2014 recommend pirfenidone treatment for patients with measured FVC ≥50% and ≤ 90% predicted and DLco ≥35% [24]. Pirfenidone was administrated at 2403 mg/day in 3 doses. The majority of patients enrolled by December 2014 obtained together with pirfenidone NAC at 3 × 600 mg based on recommendation from the clinical trials [25] and Czech IPF guidelines [24]. Since January 2015, pirfenidone has been administrated without NAC, according to the new evidence from clinical trials, mainly PANTHER trial [26, 27] and updated Czech IPF guidelines [28].

This study on a large national real-life IPF cohort showed clinically meaningful reductions in disease progression as assessed by the decline of lung functions in patients with IPF treated 2-yrs with pirfenidone comparing to no-antifibrotics. After 5-yrs, more than half of patients on pirfenidone were alive comparing to one-third on no-antifibrotics. Moreover, our data highlights the importance of the decline in DL_CO of ≥10% as a predictor of mortality in pirfenidone treated patients.

Several studies in various populations proved that pirfenidone slows-down the disease progression in terms of declining the lung functions during the first year of administration [11–18]. Nowadays, there is the need for extended follow-up [19]. Since the registration trials of IPF treatments have not been designed to estimate long-term survival, an open-label extension study (RECAP) [29, 30] based on patients from randomised controlled clinical studies CAPACITY and ASCEND [5, 6] has been designed. The RECAP study supports the safety and long-term efficacy of pirfenidone with median survival of 72.2 months, which corresponds to our data where at 5-yrs (60 months) follow-up the median OS has not been reached. Importantly, 55.9% of our patients on pirfenidone were on follow-up for 5-yrs, which is also in line with the RECAP study showing that 49% of patients from the CAPACITY trial were 5-yrs on pirfenidone follow-up [19, 30]. Other recent study estimated the mean life expectancy with pirfenidone to be 8.72 years (95% confidence interval, 7.65–10.15) [8, 31]. Nevertheless, our study brings additional proof-of-effect of the first antifibrotic treatment to the results of randomized controlled trials CAPACITY and ASCEND [5, 6] and their extension study RECAP [29, 30] in real-world settings. These observations further support pirfenidone treatment benefit in patients who continued receiving therapy.

Next, we were wondering about the dynamics of progression during the 2-yr follow-up on pirfenidone in our real-life cohort of IPF patients. Although it is crucially important to assess disease progression in IPF, there is still no consensus how to classify it [32]. The evidence-based guidelines for management of IPF suggests that an absolute decline of FVC (more than 10%) and decline DL_CO (more than 15%) is an acceptable method for assessing disease severity and estimating the risk of mortality [21]. However, some studies highlight the clinical utility of marginal declines FVC (more than 5%) and DL_CO (more than 10%) [22, 23]. In our patients on pirfenidone, the progression measured by decline in FVC (≥10%) was evident in 5.3% of patients at month 6. Similar observations (5.5%) were reported in a large cohort of 618 patients on pirfenidone in the ASCEND and CAPACITY trials [31, 33]. Also, the number of our patients progressing on pirfenidone in month 12 (10.7%) were in lines with reported data [9, 11, 13–17]. Importantly, almost twice as many patients progress on no-antifibrotic treatment comparing to pirfenidone during 1-yr follow-up.

Our study further focused on the decline of lung functions in IPF patients at 18 and 24 months after pirfenidone administration. Among patients from RECAP cohort, 16.3% experienced FVC decline ≥10% on pirfenidone at week 60 (month 15) [29, 30], compared with 16.6% in our cohort at month 18. Similar data on slow progression on pirfenidone treatment were also reported in current studies on national real-life cohorts of Danish [18] and Greek [12] IPF patients. Our study proved that even 2-years on pirfenidone administration, less than one-quarter of IPF patients progress as assessed by the decline of ≥10% FVC (17.0%) and ≥ 15% DL_CO (14.3%). When comparing pirfenidone to no-antifibrotic treatment, twice as many patients progressed on no-antifibrotic treatment in our cohort. The long-term slow-down impairment of lung function on pirfenidone and other antifibrotic treatments has an important issue also in terms of timing for lung transplantation. Prolonged time with no disease progression may increase the chance for lung transplant in IPF patients. Despite the short mean waiting time of 6 months for lung transplantation for patients with interstitial lung diseases (ILD) in the Czech Republic, the number of transplanted patients in our cohort was very low (less than 2%). The main reason for the small number of transplanted patients may be the size of requested donor lungs for IPF patients as well as the current age limit of 65 yrs. for recipients of lung transplant in the Czech Republic.

There is also evidence that pirfenidone therapy is associated with a reduction in the relative risk of mortality compared with placebo over 120 weeks [31]. We were therefore interested whether the decline in lung function on particular treatment may be associated with increased mortality in our patients as shown in previous studies [34, 35]. Indeed, the DL_CO (≥10%) declines at 6, 12, 18 and 24 months’ and DL_CO (≥15%) decline at 6, 18 and 24 months’ follow-up were associated with increased mortality in our patients on pirfenidone. This finding suggests that in some IPF patients, fibrotic processes ongoing in the lungs are not completely controlled by antifibrotic therapy, which is first seen in changes of DL_CO. Importantly, the DL_CO decline of ≥10% showed higher predictive value for mortality on pirfenidone at all investigated time intervals than FVC decline. This observation is in line with previous studies [35–37], where the DL_CO declines were more predictive of mortality risk than FVC ones. In patients with no-antifibrotics, both FVC and DL_CO declines were not predictive for mortality. This may be due to the high heterogeneity of lung function impairment in our patients treated with no-antifibrotic drugs, including more than half of patients with severe lung impairment. Our data may also suggest that the decrease in lung function in “severe” IPF is less informative in regards to mortality than in those with “mild” and “moderate” disease. Also the fact that treatment with no-antifibrotics does not lead to functional and symptomatic stabilisation together with higher number of acute exacerbations may contribute to our observation. These results further support the profit of antifibrotic treatments in IPF and need to be validated in future studies. Our study further confirmed the clinical utility of declines in DL_CO of more than 10% for the identification of risk patients with poor prognosis on pirfenidone, for whom timely transplantation is required. Therefore, we suggest the DL_CO assessment as a part of routine follow-up examinations in IPF patients on pirfenidone. The clinical usefulness the DL_CO decline as a mortality predictor deserves future investigation on larger independent cohorts. Moreover, we are aware that this retrospective study requires future testing in a prospectively recruited cohort of patients.

Despite the European Medicines Agency approving and introducing in most European countries antifibrotic treatment of IPF in 2011, many patients with confirmed IPF still do not receive approved antifibrotic treatment as shown by the current study in five European countries (France, Germany, Italy, Spain, and the UK) [38]. According to this study, in 2016 71% of “mild” IPF, 41% of “moderate” and 60% of patients with “severe” IPF did not receive any approved antifibrotic treatment. Also, in our cohort, half of the patients with no-antifibrotic treatment fulfil the Czech criteria for indication of antifibrotic treatment [28]. The majority of those patients were entering the study before introducing the commercially available antifibrotic drug. Moreover, some patients fullfilling the criteria for antifibrotic treatment migtht not receive this drug shortly after its introduction due to the need of establishment of communication between local pneumologists and ILD centres in the Czech Republic, which may only prescribe antifibrotic drugs. Although pirfenidone treatment is mainly recommended for patients with mild to moderate IPF, the recent opinion also suggests the initiation of treatment in patients with severe functional impairment. There is already a growing body of evidence that patients with advanced IPF (FVC < 50% and/or DLco < 35%) profit from pirfenidone leading to functional and symptomatic stabilisation [9–11, 39]. Despite symptomatic stabilisation and slowing down the disease progression, our study showed more deaths in a group of IPF patients with more severe pulmonary function impairment in both pirferidone and no-antifibrotic treatments. Therefore, efforts for early diagnosis of the condition increases as there is evidence about more effective therapeutic efficiency, less complications and lower mortality comparing to severe disease. More studies are needed to include patients with severe functional impairment in antifibrotic treatment indications by the health authorities. Our data further supports the importance of registries in the understanding of this devastating rare disease, disease progression, quality of life and outcomes on the treatment.

Our data proved that pirfenidone has a 2-yrs lasting effect on the slowing down of lung function decline, as well as on reducing mortality compared to no-antifibrotic treatments in IPF patients from the Czech part of the EMPIRE registry. Our data provide further evidence of the effect of the first antifibrotic treatment in IPF to the results of randomized controlled trials in real-world settings. The 5-yrs OS was markedly higher in patients treated with pirfenidone compared to no-antifibrotic treatment, with more than half of patients on pirfenidone still living comparing to one-third on no-antifibrotics. Finally, the DL_CO assessment should be part of routine follow-up investigations in IPF patients on pirfenidone, as its decline was highly associated with mortality and those risk patients are candidates for timely lung transplantation.