Abstract
Idiopathic pulmonary fibrosis (IPF) is a progressively fibrotic disease, with no effective treatment and a median survival time of 2–5 yrs. The search for effective treatment has involved numerous clinical trials of investigational agents without significant success until 2011, when European approval was given for the first treatment for IPF, pirfenidone. Four key clinical trials supported the efficacy and tolerability of pirfenidone.
In recently published results from two phase III randomised, double-blind, placebo-controlled, multinational trials evaluating pirfenidone (studies 004 and 006), patients with mild-to-moderate IPF were screened for eligibility using the following functional criteria: forced vital capacity (FVC) ≥50% predicted; diffusing capacity of the lung for carbon monoxide ≥35%; and 6-min walk test (6MWT) distance ≥150 m.
Only study 004 met the primary end-point of change in per cent predicted FVC at week 72 (p<0.001). Pooled analysis of primary end-point data from both studies also showed that pirfenidone significantly reduced the decline in per cent predicted FVC compared to placebo (p<0.005). Evidence of beneficial effects of pirfenidone treatment was also observed with regard to several secondary end-points, including progression-free survival time, categorical FVC change, and mean change from baseline to week 72 in 6MWT distance.
Pirfenidone was generally well tolerated, with the most common side-effects being gastrointestinal discomfort and photosensitivity. The pooled study results, coupled with recent data regarding the prognostic significance of changes in FVC and 6MWT, provide further evidence of a clinically meaningful treatment benefit with pirfenidone in patients with IPF.
Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal fibrotic lung disease with a median survival of 2–5 yrs. This debilitating disease occurs predominantly in older adults, with an estimated prevalence of 1.6 to 1.7 per 10,000 [1, 2]. Progressive deterioration of pulmonary function is inevitable, which increasingly limits the normal physical activity of the patient [3, 4]. The pace and magnitude of disease progression is often unpredictable [5], with apparently stable patients often suffering episodes of acute exacerbation [6, 7].
PROGNOSTIC FACTORS
Pulmonary function test values are often used as predictive factors of survival in IPF. A decline in forced vital capacity (FVC) has consistently been shown to be a strong predictor of mortality, and is frequently used as an end-point in clinical trials [8, 9]. A decline in FVC of ≥10% in a 6-month period is associated with a nearly five-fold increase in the risk of mortality [9–12]. Indeed, agents that attenuate the decline in FVC are anticipated to play an important role in the management of patients with IPF.
Other prognostic factors commonly used as end-points in IPF clinical trials include: diffusing capacity of the lung for carbon monoxide (DL,CO), a decrease of 15% of the absolute value has been associated with increased risk of mortality [10, 13–15]; a change in alveolar–arterial oxygen tension difference of >15 mmHg after 12 months has been shown to be predictive of survival [10, 14]; the 6-min walk test (6MWT), which has been widely used in clinical practice, a shorter walk distance and delayed heart rate recovery after 6MWT have been associated with an increased risk of mortality [8, 10, 16–19].
THE SEARCH FOR NEW THERAPIES AND RECENTLY COMPLETED TRIALS
Since 2001, the search for new therapies to treat IPF has intensified, as demonstrated by an increase in the number of registered clinical trials. However, many of these clinical trials have failed to demonstrate a statistically significant treatment effect on the primary end-point [20].
In 2005, results were published from the IFIGENIA (Idiopathic Pulmonary Fibrosis International Group Exploring N-Acetylcysteine I Annual) trial, which was conducted to investigate whether a high dose of N-acetylcysteine (NAC), administered over the course of 1 yr to patients receiving treatment with prednisone and azathioprine, would slow the functional deterioration in patients with IPF [21]. This was a double-blind, randomised, placebo-controlled, multicentre study with primary end-points of absolute changes in vital capacity (VC) and DL,CO between baseline and 12 months. The trial showed that patients receiving prednisone, azathioprine and NAC for 12 months had a significantly slower rate of deterioration of both VC and DL,CO than the patients who received only prednisone and azathioprine therapy, suggesting that the addition of NAC could aid preservation of pulmonary function in patients with IPF. There is, however, considerable uncertainty about the clinical relevance of this result due to a drop-out rate of ∼30% and the absence of a suitable control arm [20, 21].
The potential benefit of NAC and triple combination therapy (prednisolone, azathioprine and NAC) is currently being evaluated in the PANTHER (Prednisone, Azathioprine, N-acetylcysteine, a Trial tHat Evaluates Response) trial coordinated by the National Heart, Lung and Blood Institute (Bethesda, MD, USA). However, on October 21, 2011 a press release was published announcing that the triple therapy arm of this trial had been discontinued due to an excess of deaths or emergency hospitalisations, and a higher prevalence of serious adverse events compared with the comparative arms of placebo and NAC alone [22]. As the trial is continuing with the NAC and placebo arms, the detailed results of this study are not yet known. However, the triple therapy cannot be considered a standard therapy in patients with IPF [22, 23], and the potential benefit of NAC requires further evaluation.
A recent phase II trial assessed the efficacy and safety of four different oral doses (50 mg q.d., 50 mg b.i.d., 100 mg b.i.d. or 150 mg b.i.d.) of the tyrosine kinase inhibitor BIBF 1120 compared to placebo in 432 patients with IPF. The primary end-point was the annual rate of decline in FVC [24]. Secondary end-points included acute exacerbations, quality of life (measured with the St George’s Respiratory Questionnaire (SGRQ)) and total lung capacity. The predefined, multiplicity-corrected primary end-point did not differ significantly between the group of patients receiving the highest BIBF 1120 dose (150 mg b.i.d.) and the placebo group. The annual rate of decline in FVC in the group receiving 150 mg of BIBF 1120 b.i.d. was 0.06 L (95% CI -0.14–0.02 L), as compared with 0.19 L in the placebo group (95% CI -0.26– -0.12 L) (p=0.06 with the closed testing procedure for multiplicity; p=0.01 with hierarchical testing) [24]. The incidence of acute exacerbations was 2.4% per 100 patient-yrs in patients receiving 150 mg of BIBF 1120 b.i.d. and 15.7% per 100 patient-yrs in the placebo group (p=0.02). A nonsignificant decrease in the SGRQ was observed. Treatment was discontinued by 30.6% of patients receiving BIBF 1120 at 150 mg b.i.d. and by 25.9% of patients receiving placebo. Further studies are required to evaluate the potential benefit of BIBF 1120 in reducing the decline in lung function [24].
Numerous other targets have been explored in an attempt to find an effective treatment for IPF. Bosentan is a dual endothelin receptor antagonist, and is an effective treatment for pulmonary arterial hypertension, a disease characterised by progressive remodelling of the pulmonary vasculature [25]. Due to its anti-inflammatory and anti-fibrotic properties, it was suggested that bosentan might be potentially useful in the treatment of IPF. However, bosentan was not found to be superior to placebo in terms of 6MWT distance (primary end-point) in the BUILD-1 (Bosentan Use in Interstitial Lung Disease) study. A trend was observed in favour of bosentan for the secondary end-point of time to death or disease progression, and this was more pronounced in patients with IPF diagnosed by surgical lung biopsy [25]. A further study, BUILD-3, used the primary end-point of time to disease worsening or death but found no significant difference compared with placebo [26]. Taken together, the results of these two studies suggest that bosentan is unlikely to be of benefit to IPF patients.
Imatinib mesylate is another agent that has been investigated for the potential treatment of IPF. As imatinib mesylate is a tyrosine kinase inhibitor with activity against platelet-derived growth factor receptor, it was considered that this may be a useful agent in IPF treatment [27]. However, a phase II study of 119 patients with IPF found no significant benefit of treatment with imatinib mesylate compared with placebo in terms of the primary end-point of time to disease progression. No effects on lung function were observed, and it was concluded that imatinib mesylate is not an effective therapy for patients with IPF [27].
Another potential approach is the use of a phosphodiesterase type-5 inhibitor, such as sildenafil, which has been shown to preferentially improve pulmonary ventilation [28]. Despite the suggestion that sildenafil may also have beneficial effects for patients with IPF, a phase III study found that sildenafil treatment did not improve 6MWT distance compared with placebo. Small improvements were seen in the extent of dyspnoea and quality of life in favour of sildenafil. These were considered clinically significant, with the investigators suggesting that sildenafil may have some use in improving symptoms for patients with advanced IPF [28].
The presence of elevated levels of tumour necrosis factor (TNF)-α in models of pulmonary fibrosis provided rationale for the investigation of etanercept for the treatment of IPF [29]. Raghu et al. [29] designed an exploratory placebo-controlled trial to determine whether etanercept had a positive effect on declining lung function compared with placebo in IPF patients. Although etanercept was well tolerated, no statistically significant differences were observed in lung function parameters, although this study recruited only a small number of patients (n=88).
King et al. [30] studied the use of interferon-γ1b in a phase III study of patients with IPF. The primary end-point of this study was improvement in overall survival versus placebo. At the second interim analysis of this study, the required minimum benefit had not been demonstrated, and so the study was stopped. The authors reported that this study conclusively demonstrated a lack of improvement in overall survival of IPF patients with interferon- γ1b [30].
Despite few positive outcomes, the results of these studies showed that randomised, controlled trials are feasible in investigating potential new treatments for this progressive disease.
Pirfenidone for the treatment of mild-to-moderate IPF
Pirfenidone (5-methyl-1-phenyl-2-[1H]-pyridone) is an orally administered drug that has exhibited anti-fibrotic and anti-inflammatory properties in a variety of in vitro and in vivo studies [31–35]. There is evidence to show that pirfenidone mitigates fibroblast proliferation, fibrosis-associated proteins and cytokines (transforming growth factor-β and platelet-derived growth factor), biosynthesis and accumulation of extracellular matrix, as well as accumulation of inflammatory cells and TNF-α synthesis [31–35].
Pirfenidone was approved by the European Commission in February 2011 following evaluation in one phase II and three phase III clinical trials in patients with IPF [36–38]. Pirfenidone is indicated for the treatment of mild-to-moderate IPF patients. Mild-to-moderate disease was characterised in the pivotal phase III studies by the following functional criteria: FVC ≥50% of predicted, DL,CO ≥35% pred and a 6MWT distance of ≥150 m [38].
Phase III trial of Japanese patients
Based on a positive phase II study [36], a multicentre, double-blind, placebo-controlled, randomised phase III clinical trial to determine the efficacy and safety of pirfenidone in 275 patients with IPF was conducted in Japan over a period of 52 weeks [37]. Patients were randomised to receive pirfenidone 1,800 mg·day−1, pirfenidone 1,200 mg·day−1 or placebo in the ratio of 2:1:2, with 267 patients being evaluated for the efficacy of pirfenidone. The dose of pirfenidone was increased in a stepwise manner up to the treatment dose over 4 weeks. The primary end-point was revised to change in VC from baseline to 52 weeks before unblinding of the study (the primary end-point was previously arterial oxygen saturation measured by pulse oximetry (Sp,O2) during the 6-min steady-state exercise test). The decision to revise the primary end-point was based on the evolved knowledge of assessment with objective measurements in IPF, as well as the lack of validation in the study of the steady-state exercise test and problems in reproducing Sp,O2 measurements during the 6MWT. Secondary end-points included progression-free survival (defined as the time until the first progressive event, i.e. either decrease in VC of >10% or death) and change in the lowest Sp,O2 during the 6-min steady-state exercise test [37].
This study found significant differences between the pirfenidone 1,800 mg·day−1 group and the placebo group for both the primary (decline in VC) and secondary progression-free survival end-points. There was a 44% reduction in the VC decline in favour of pirfenidone compared with placebo (change in VC: pirfenidone -0.09 L and placebo -0.16 L; p=0.0416) (fig. 1). Pirfenidone was also associated with a significant increase in progression-free survival (p=0.0280). With regard to safety, pirfenidone was relatively well tolerated. The most common adverse event observed in both the high- and low-dose pirfenidone groups was photosensitivity (51% and 53%, respectively), which was rated as mild in the majority of patients [37], and has been documented as a side-effect associated with pirfenidone in previous studies [36, 39]. The data from this phase III trial led to the approval of pirfenidone for IPF patients in Japan in 2008.
Multinational phase III trials 004 and 006: CAPACITY programme
Pirfenidone has been studied in two concurrent, similar phase III trials (studies 004 and 006), which were conducted at 110 sites across North America, Australia and Europe. Both trials were randomised, double-blind, placebo-controlled studies with a treatment period of 72 weeks. The studies were designed to confirm the results of a phase II study suggesting that pirfenidone reduces the deterioration in lung function in patients with IPF [38]. The data from these two phase III trials led to the approval of pirfenidone for IPF patients in the European Union in 2011.
Eligible patients were aged 40–80 yrs with a confident diagnosis of IPF in the previous 48 months and no evidence of improvement in measures of disease severity over the preceding year. Additional criteria for enrolment included: an FVC of ≥50% pred; DL,CO ≥35% pred; FVC or DL,CO of ≤90% pred; and a 6MWT distance of ≥150 m. For patients aged >50 yrs and those not meeting the protocol criteria for definite IPF by use of high-resolution computed tomography, a lung biopsy sample showing usual interstitial pneumonia was required [38].
In study 004, patients were assigned to oral pirfenidone 2,403 mg·day−1 or 1,197 mg·day−1, or placebo in a 2:1:2 ratio, while in study 006, patients were assigned to pirfenidone 2,403 mg·day−1 or placebo in a 1:1 ratio. In both studies, pirfenidone was administered with food three times a day and increased to full dose over 2 weeks. In study 004, the lower dose of 1,197 mg·day−1 was included to investigate a potential dose–response effect [38].
The primary end-point of both studies was change in FVC % pred from baseline to week 72. The secondary end-points at week 72 for both studies (table 1) included: categorical decline in FVC ≥10%; progression-free survival (time to confirmed decline ≥10% pred decline in FVC, ≥15% pred decline in DL,CO or death); mean change in 6MWT distance; mean change in DL,CO % pred; mean change in dyspnoea score (using the University of California San Diego Shortness of Breath Questionnaire); mean percentage change in worst Sp,O2 during 6MWT; and time to worsening IPF (time to acute exacerbation, death, lung transplantation or admission to hospital for respiratory problems). Categorical change in high-resolution computed tomography diagnosed fibrosis was included as a secondary end-point only in study 006. Both studies included mortality as an exploratory end-point [38].
In study 004, pirfenidone 2,403 mg·day−1 significantly reduced mean decline from baseline to week 72 in per cent predicted FVC compared with placebo (-8.0±16.5% versus -12.4±18.5%, respectively; p=0.001), as well as the proportion of patients with FVC decline ≥10%. This treatment effect was evident between weeks 24 and 72 (fig. 2). A pirfenidone effect was confirmed (p=0.0007) after repeated measures analysis of the per cent predicted change in FVC across all assessment time-points. In the pirfenidone 1,197 mg·day−1 group, the primary end-point outcomes were intermediate to the 2,403 mg·day−1 pirfenidone and placebo groups [38].
Study 006 did not meet the primary efficacy end-point, as there was no significant difference between the pirfenidone and placebo groups in the mean decline in per cent predicted FVC at week 72 (-9.0±19.6% and -9.6±19.1%, respectively) (fig. 2). The difference in FVC outcomes in the two studies might be partly attributable to a lower than expected rate of FVC decline in study 006 after 1 yr. Although the magnitude of decline over time was similar in the two pirfenidone groups, those in the two placebo groups differed [38]. However, the data from this study generally supported those from study 004, with a positive treatment effect of pirfenidone being observed at all time-points from weeks 12 to 48 but not at later time-points [38].
A pirfenidone treatment effect on per cent predicted FVC at week 72 was supported by a pre-specified analysis of the pooled data from both studies (p=0.005). Mean decline in percentage predicted FVC was -8.5% and -11.0% for the pirfenidone 2,403 mg·day−1 and placebo groups, respectively (fig. 2). Additionally, the pooled analysis demonstrated a 30% reduction in the percentage of patients with a categorical decline in FVC ≥10% at week 72 (p=0.003), a 31% reduction in the mean decline in 6MWT distance (p>0.001) and a 26% reduction in the risk of death or disease progression (hazard ratio (HR) 0.74, 95% CI 0.57–0.96; p=0.025) (table 1) [38].
Although the study was not powered for mortality analysis, a pooled analysis of the exploratory end-point of mortality revealed that the HRs for all-cause mortality (p=0.315) and mortality related to IPF at any time during the study favoured pirfenidone over placebo (p=0.117). This was also the case with on-treatment IPF-related mortality, which occurred in 3% of patients treated with pirfenidone and 7% of those given placebo (p=0.03) (table 2) [38].
Pirfenidone was shown to be safe and generally well tolerated at the 2,403 mg·day−1 dose in both studies [38]. There was no significant difference in the number of patients experiencing serious treatment-emergent adverse events between the pooled pirfenidone and placebo groups (33% and 31%, respectively) (table 3). Nearly all patients in the pirfenidone 2,403 mg·day−1 group (pooled data from both studies) experienced at least one treatment-emergent adverse event, with the most common adverse events being gastrointestinal (nausea 36%, dyspepsia 19%, vomiting 14% and anorexia 11%), skin disorders (rash 32% and photosensitivity 12%) and dizziness (18%) (table 3). These adverse events were consistent with the known safety profile of pirfenidone and were usually mild to moderate in severity [38]. Adverse events led to discontinuation of treatment in 15% of the pirfenidone groups and 9% of the pooled placebo groups. The most common cause for treatment discontinuation was IPF (3% both in the pirfenidone and placebo group). The only other causes of treatment discontinuation in the pooled pirfenidone groups were nausea (1%) and rash (1%). Generally, the most common adverse effects of pirfenidone treatment were manageable by temporary dose modification [38].
CONCLUSIONS
There has been considerable advancement in terms of research into prognostic factors, with decline in percentage of FVC being found to be a predictor of mortality risk. Until recently, therapeutic developments had lagged somewhat, but the increase in the number of clinical trials has been encouraging. However, many of these trials failed to show significant treatment benefit against this challenging disease. Further studies are required to evaluate the potential benefit of NAC and BIBF 1120 in IPF. The first major step forward has been the European approval of pirfenidone for patients with mild-to-moderate IPF. Pirfenidone has demonstrated statistically significant and clinically meaningful effects in clinical trials. Overall, pirfenidone provides a significant treatment benefit for patients with IPF and represents an appropriate option as first-line therapy for these patients.
Acknowledgments
I received medical writing assistance from IntraMed Communications (Milan, Italy).
Footnotes
Statement of Interest
V. Cottin has received fees for speaking from Intermune, Boehringer Ingelheim and Actelion; and has participated as investigator to clinical trials sponsored by InterMune, Boehringer and Actelion, and as a member of a steering committee for a clinical trial sponsored by Boehringer Ingelheim.
Provenance
Publication of this peer-reviewed article was sponsored by InterMune International AG, Muttenz, Switzerland (article sponsor, European Respiratory Review issue 124).
- Received February 3, 2012.
- Accepted February 21, 2012.
- ©ERS 2012