Abstract
Objective
We compared the haemodynamic effects of riociguat in patients with inoperable chronic thromboembolic pulmonary hypertension (CTEPH) or persistent/recurrent CTEPH after pulmonary endarterectomy in the Chronic Thromboembolic Pulmonary Hypertension Soluble Guanylate Cyclase–Stimulator Trial 1 study.
Methods
Patients with inoperable or persistent/recurrent CTEPH (n=261; mean± SD age 59±14 years; 66% women) were randomised to riociguat (up to 2.5 mg three times daily) or placebo. Haemodynamic parameters were assessed at baseline and week 16.
Results
Riociguat decreased pulmonary vascular resistance (PVR) in inoperable (n=189; least-squares mean difference: −285 dyn s/cm5 (95% CI −357 to −213); p<0.0001) and persistent/recurrent (n=72; −131 dyn s/cm5 (95% CI −214 to −48); p=0.0025) patients. Cardiac index improved in inoperable patients by a least-squares mean difference of +0.6 L/min/m2 (95% CI 0.4 to 0.7; p<0.0001), while in persistent/recurrent patients the change was +0.2 L/min/m2 (95% CI −0.1 to 0.5; p=0.17). Mean pulmonary artery pressure decreased in inoperable and persistent/recurrent patients(−4.7 mm Hg (95% CI −6.9 to −2.6; p<0.0001 and −4.8 mm Hg (–8.2 to −1.5; p=0.0055), respectively). For all patients, changes in 6 min walk distance correlated with changes in PVR (r=−0.29 (95% CI −0.41 to −0.17); p<0.0001) and cardiac index (r=0.23 (95% CI 0.10 to 0.35); p=0.0004).
Conclusions
Riociguat improved haemodynamics in patients with inoperable CTEPH or persistent/recurrent CTEPH.
Trial registration number
Introduction
Chronic thromboembolic pulmonary hypertension (CTEPH) is a chronic, life-threatening disease associated with significant morbidity and mortality.1 The disease is characterised by the obstruction of pulmonary vasculature by residual organised thrombi,2 which if left untreated, leads to the development of pulmonary hypertension (PH), progressive right ventricular (RV) dysfunction and ultimately death.3 4
Pulmonary endarterectomy (PEA) is the gold standard treatment for CTEPH and the only available therapy that has the potential to cure the disease.5–7 However, some patients may be deemed inoperable due to the occlusion of distal vessels, existing comorbidities that increase the risks of surgery, lack of access to expert surgical centres or patient refusal for surgery.5 8–10 Furthermore, approximately 5%–35% of patients have persistent/recurrent PH after PEA.11–14 Until recently there were no approved pharmacotherapies to treat some of these patients,6 specifically those deemed technically inoperable due to distal disease and patients with persistent PH following PEA. Previous randomised controlled studies of pulmonary arterial hypertension (PAH)-targeted medications in patients with inoperable CTEPH have shown variable clinical efficacy.15 16
Riociguat is the first member of the soluble guanylate cyclase (sGC) stimulator class of therapeutic agents.17–20 It has a dual mode of action: sensitising sGC to endogenous nitric oxide (NO) by stabilising NO-sGC binding and directly stimulating sGC independently of NO via a different binding site.19 20 In the phase III Chronic Thromboembolic Pulmonary Hypertension Soluble Guanylate Cyclase–Stimulator Trial 1 (CHEST-1) study, riociguat improved 6 min walk distance (6MWD) and a range of secondary end points, including pulmonary vascular resistance (PVR), N-terminal prohormone of brain natriuretic peptide (NT-proBNP) levels and WHO functional class in patients with CTEPH.21 Based on these results, riociguat is, to date, the only pharmacotherapy approved for the treatment of inoperable or persistent/recurrent CTEPH.6 7 22
Here we present a detailed analysis of the haemodynamic data from the CHEST-1 study in subgroups of patients with inoperable CTEPH or persistent/recurrent PH after PEA.
Methods
Study population
The CHEST-1 study methodology has been published previously.21 Patients with CTEPH who were adjudicated to be technically inoperable or had persistent/recurrent PH after PEA were eligible if they had a 6MWD of 150–450 m, PVR >300 dyn s/cm5 and mean pulmonary artery pressure (mPAP) ≥25 mm Hg. Patients who received an endothelin receptor antagonist, prostacyclin analogue, phosphodiesterase type 5 inhibitor or NO donor within the 3 months before study entry were not eligible for the study.
Patients with CTEPH who were considered inoperable by study investigators underwent prospective adjudication by an adjudication committee (nominated by the sponsor) composed of six experienced PEA surgeons. A local decision was permitted in cases where an experienced surgeon collaborated with the study centre in the context of the patient's regular diagnostic workup. Technical inoperability, based on previously published criteria,6 23 was determined using at least a pulmonary angiogram supplemented by a ventilation-perfusion (VQ) scan (as the preferred method) or alternatively a CT pulmonary angiogram (minimum 64-slice spiral CT with contrast medium) supplemented by a VQ scan. Medical history and haemodynamic data (at least mean right atrial pressure (RAP), mPAP, PVR, cardiac output and pulmonary artery wedge pressure (PAWP)) were also provided.
The research protocol was approved by local ethics committees and written informed consent was obtained from patients in accordance with the Declaration of Helsinki. The study is registered at ClinicalTrials.gov (identifier NCT00855465).
Study design
CHEST-1 was a 16-week, double-blind, randomised, placebo-controlled, multicentre study conducted in 89 centres across 26 countries between February 2009 and June 2012. An interactive voice-response system and a computer-generated random code (provided by Bayer Randomisation Management) were used to randomly assign patients in a 1:2 ratio to placebo or oral riociguat administered at doses that were individually adjusted for each patient up to 2.5 mg three times daily. During the initial 8 weeks of the study, the dose of riociguat was adjusted every 2 weeks according to an individual plan based on the patient's systolic blood pressure (SBP) and signs or symptoms of hypotension. From a starting dose of 1 mg three times daily, the dose of riociguat was increased (by 0.5 mg three times daily) if trough SBP was ≥95 mm Hg; maintained if SBP was 90–94 mm Hg and decreased (by 0.5 mg three times daily) if SBP was <90 mm Hg without symptomatic hypotension. The dose reached at the end of the 8-week adjustment phase was considered to be the optimal dose for the individual patient and was continued for a further 8 weeks.
Randomised patients were seen at baseline and at weeks 2, 4, 6, 8, 12 and 16. Haemodynamic parameters were assessed by right heart catheterisation (RHC) (Swan Ganz catheterisation and thermodilution methodology) at baseline and week 16.
Outcome measures
The primary outcome of CHEST-1 was the change in 6MWD from baseline to week 16.21 Secondary outcomes included the changes from baseline to week 16 in PVR, NT-proBNP and WHO functional class and time to clinical worsening. Exploratory outcomes included the change from baseline to week 16 in a range of additional haemodynamic parameters, including RAP, PAWP, cardiac output and mixed venous oxygen saturation (SvO2). Calculated haemodynamic parameters, determined using standard formulas, included mean arterial pressure (MAP), mPAP, PVR, systemic vascular resistance (SVR), pulmonary diastolic pressure gradient (DPG) and cardiac index. Adverse events (AEs) and laboratory variables were assessed throughout the study and during the safety follow-up period.
Statistical analysis
The statistical analysis plan for CHEST-1 has been published previously.21 The changes from baseline to week 16 in haemodynamic parameters, 6MWD and NT-proBNP were analysed by analysis of covariance, followed by a test of normality of the residuals and a non-parametric-stratified Wilcoxon test on rejection. Predefined analysis of the changes in 6MWD and post hoc analysis of the changes in haemodynamic parameters in the inoperable and post-PEA subgroups was undertaken using the same methods. The interaction between change from baseline to week 16 in the inoperable and persistent/recurrent subgroups was assessed using analysis of covariance. A Spearman's ranked correlation was used to determine the correlation between change in 6MWD and change in PVR and cardiac index at week 16.
Missing values for haemodynamic parameters and NT-proBNP, where the patient died or withdrew from the study, were imputed according to the last post-baseline measurement. In the case of withdrawal with no post-baseline measurements, the baseline value was used. In the case of 6MWD, the last observed value was taken, except in cases of death or clinical worsening without a termination visit, where worst values (0 m) were imputed.
AEs during the study period included all AEs that started or worsened from the time of administration of the first dose of the study drug until 2 days after the administration of the last dose.
Results
Baseline demographics and haemodynamics
Patient characteristics were well balanced between the groups at baseline and the majority of patients had WHO functional class II or class III symptoms (table 1). There were more patients in the inoperable CTEPH subgroup (n=189) compared with the persistent/recurrent PH following PEA subgroup (n=72). The 6MWD was marginally higher at baseline in patients with persistent/recurrent PH following PEA than in those patients with inoperable CTEPH (table 1). Baseline haemodynamic values in the overall study population were characteristic of a general CTEPH population and included elevated PVR and mPAP (table 2).8 However, haemodynamic impairments were slightly less severe in the persistent/recurrent PH after PEA subgroup at baseline compared with the inoperable CTEPH subgroup (table 2). Patient disposition in CHEST-1 has been published previously.21
Table 1.
Baseline demographics for the overall group and the inoperable and persistent/recurrent PH following PEA subgroups
| Inoperable CTEPH |
Persistent/recurrent PH following PEA |
All patients |
||||
|---|---|---|---|---|---|---|
| Characteristic | Riociguat (n=121) | Placebo (n=68) | Riociguat (n=52) | Placebo (n=20) | Riociguat (n=173) | Placebo (n=88) |
| Female sex, n (%) | 86 (71) | 45 (66) | 32 (62) | 9 (45) | 118 (68) | 54 (61) |
| Race, n (%) | ||||||
| White | 76 (63) | 49 (72) | 44 (85) | 16 (80) | 120 (69) | 65 (74) |
| Black | 5 (4) | 0 | 2 (4) | 1 (5) | 7 (4) | 1 (1) |
| Asian | 32 (26) | 17 (25) | 5 (10) | 3 (15) | 37 (21) | 20 (23) |
| Multiple | 1 (1) | 0 | 0 | 0 | 1 (1) | 0 |
| Not reported | 7 (6) | 2 (3) | 1 (2) | 0 | 8 (5) | 2 (2) |
| Mean age (SD), years | 59 (14) | 60 (12) | 60 (14) | 57 (15) | 59 (14) | 59 (13) |
| Mean BMI (SD), kg/m2 | 27 (5) | 28 (5) | 28 (7) | 28 (6) | 27 (6) | 28 (5) |
| WHO FC, n (%)* | ||||||
| I | 2 (2) | 0 | 1 (2) | 0 | 3 (2) | 0 |
| II | 38 (31) | 18 (26) | 17 (33) | 7 (35) | 55 (32) | 25 (28) |
| III | 75 (62) | 49 (72) | 32 (62) | 11 (55) | 107 (62) | 60 (68) |
| IV | 6 (5) | 1 (1) | 2 (4) | 1 (5) | 8 (5) | 2 (2) |
| Missing | 0 | 0 | 0 | 1 (5) | 0 | 1 (1) |
| Mean 6MWD (SD), m | 335 (83) | 351 (75) | 360 (78) | 374 (72) | 342 (82) | 356 (75) |
*Data may not add up to 100% due to rounding.
6MWD, 6 min walk distance; BMI, body mass index; CTEPH, chronic thromboembolic pulmonary hypertension; PEA, pulmonary endarterectomy; PH, pulmonary hypertension; WHO FC, WHO functional class.
Table 2.
BL and change from BL in haemodynamic parameters in the inoperable and persistent/recurrent PH following PEA subgroups
| Parameter | Inoperable CTEPH |
Persistent/recurrent PH after PEA |
Interaction p value for difference between inoperable and persistent/ recurrent subgroups |
||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Riociguat |
Placebo |
LS mean difference (95% CI) | Riociguat vs placebo p-value |
Riociguat |
Placebo |
LS mean difference (95% CI) | Riociguat vs placebo p value |
||||||||||
| n | BL* | Change from BL at week 16* | n | BL* | Change from BL at week 16* | n | BL* | Change from BL at week 16* | n | BL* | Change from BL at week 16* | ||||||
| PVR, dyn s/cm5 | 105 | 867 (471) | −257 (279) | 63 | 851 (423) | +33 (292) | −285 (−357 to −213) | <0.0001 | 46 | 618 (252) | −154 (127) | 19 | 540 (172) | −11 (205) | −131 (−214 to −48) | 0.0025 | 0.0089 |
| SVR, dyn s/cm5 | 106 | 1926 (692) | −537 (559) | 60 | 1887 (675) | +56 (615) | −570 (−711 to −430) | <0.0001 | 47 | 1688 (451) | −272 (484) | 17 | 1767 (529) | −121 (551) | −183 (−449 to 83) | 0.17 | 0.0080 |
| mPAP, mm Hg | 109 | 47 (13) | −4 (7) | 65 | 47 (9) | +1 (7) | −4.7 (−6.9 to −2.6) | <0.0001 | 47 | 40 (10) | −5 (6) | 19 | 37 (8) | +1 (7) | −4.8 (−8.2 to −1.5) | 0.0055 | 0.8290 |
| MAP, mm Hg | 108 | 96 (12) | −10 (13) | 61 | 96 (11) | −0.4 (11) | −9.5 (−12.7 to −6.3) | <0.0001 | 47 | 93 (12) | −7 (10) | 17 | 94 (10) | 0.1 (16) | −8.2 (−14.1 to −2.3) | 0.0076 | 0.7941 |
| RAP, mm Hg | 110 | 8.3 (5.3) | −0.8 (5.4) | 65 | 9.2 (6.1) | −0.7 (5.6) | −0.6 (−2.1 to 0.9) | 0.45 | 47 | 9.3 (5.0) | −1.6 (4.5) | 19 | 6.6 (3.4) | +0.1 (3.3) | −0.2 (−2.1 to 1.7) | 0.85 | 0.8652 |
| Cardiac output, L/min | 108 | 4.1 (1.4) | +0.8 (1.1) | 64 | 4.0 (1.4) | −0.1 (1.1) | +1.0 (0.7 to 1.3) | <0.0001 | 47 | 4.2 (0.9) | +0.7 (1.1) | 19 | 4.2 (1.1) | +0.3 (0.9) | +0.4 (−0.2 to 1.0) | 0.14 | 0.0515 |
| Cardiac index, L/min/m2 | 108 | 2.3 (0.7) | +0.5 (0.6) | 64 | 2.2 (0.7) | −0.1 (0.6) | +0.6 (0.4 to 0.7) | <0.0001 | 47 | 2.3 (0.5) | +0.4 (0.5) | 19 | 2.2 (0.5) | +0.2 (0.5) | +0.2 (−0.1 to 0.5) | 0.17 | 0.0408 |
| SvO2, % | 102 | 62 (10) | +4 (10) | 59 | 61 (9) | −1 (11) | +4.9 (1.9 to 7.9) | 0.0014 | 43 | 63 (9) | +1 (7) | 18 | 64 (10) | −0.1 (12) | +1.0 (−3.1 to 5.0) | 0.63 | 0.1336 |
| PAWP, mm Hg | 105 | 9.0 (3.2) | +0.8 (3.6) | 64 | 8.8 (3.6) | −0.1 (3.6) | +0.9 (−0.1 to 1.9) | 0.082 | 46 | 9.8 (3.3) | +0.2 (4.0) | 19 | 9.5 (3.3) | +1.0 (6.3) | −0.6 (−2.9 to 1.7) | 0.61 | 0.1162 |
| dPAP, mm Hg | 109 | 29.8 (11.0) | −3.1 (6.1) | 65 | 29.0 (7.4) | +0.9 (7.6) | – | – | 47 | 25.2 (7.0) | −3.0 (6.1) | 19 | 23.1 (4.9) | −0.2 (6.6) | – | – | – |
| DPG, mm Hg | 105 | 20.7 (10.6) | −4.0 (6.4) | 64 | 20.0 (7.5) | +0.9 (7.8) | −4.8 (−6.9 to −2.7) | <0.0001 | 46 | 15.5 (6.8) | −3.3 (6.2) | 19 | 13.6 (5.6) | −1.2 (7.7) | −1.3 (−4.7 to 2.1) | 0.45 | 0.1139 |
*Data shown are mean (SD).
BL, baseline; CTEPH, chronic thromboembolic pulmonary hypertension; dPAP, diastolic pulmonary artery pressure; DPG, diastolic pressure gradient; LS, least-squares; MAP, mean arterial pressure; mPAP, mean pulmonary artery pressure; PAWP, pulmonary artery wedge pressure; PEA, pulmonary endarterectomy; PH, pulmonary hypertension; PVR, pulmonary vascular resistance; RAP, right atrial pressure; SvO2, mixed venous oxygen saturation; SVR, systemic vascular resistance.
Dosing
In the riociguat treatment group, 77% of patients were receiving the maximum dose of riociguat (2.5 mg three times daily) at week 16, 12% of patients were receiving 2.0 mg three times daily, 6% of patients were receiving 1.5 mg three times daily, 4% of patients were receiving 1.0 mg three times daily and 1% of patients were receiving 0.5 mg three times daily.
Haemodynamic parameters
In the overall population, riociguat significantly improved a range of haemodynamic parameters at week 16 compared with placebo. PVR significantly decreased in the riociguat group (−29%) compared with placebo (+3%) by a least-squares (LS) mean difference of 246 dyn s/cm5 (95% CI −303 to −190; p<0.0001) (figure 1). Cardiac index significantly increased in the riociguat group (+20%) versus placebo (−<1%) by an LS mean difference of 0.5 L/min/m2 (95% CI 0.3 to 0.6; p<0.0001) (figure 2). Significant changes were also observed in SVR (p<0.0001), mPAP (p<0.0001), cardiac output (p<0.0001), SvO2 (p=0.001), MAP (p<0.0001), dPAP (p=0.0002) and DPG (p<0.0001). RAP and PAWP did not show relevant elevations at baseline and were unchanged at week 16. Mean±SD SBP decreased in the riociguat arm by −10±14 mm Hg (from 119±15 mm Hg; n=173), whereas in the placebo group mean±SD SBP decreased by −5±15 mm Hg (from 123±16 mm Hg at baseline; n=88). No clinically relevant changes in heart rate were observed during the study; in the riociguat group, mean±SD heart rate was 78±12 bpm at baseline and 79±11 bpm at week 16; in the placebo group, mean±SD heart rate was 76±12 bpm and 78±13 bpm at baseline and week 16, respectively. Mean±SD arterial oxygen saturation decreased from baseline to week 16 by 1.5±4.4% in the riociguat group (n=152) and by 3.1±8% in the placebo group (n=80).
Figure 1.
Boxplots for pulmonary vascular resistance (PVR) at baseline (BL) and CHEST-1 week 16 in the overall population and the inoperable CTEPH and persistent/recurrent PH after PEA subgroups. LS mean treatment effect (95% CI) was determined using ANCOVA. Box: 25th to 75th percentile; horizontal line: median; cross: arithmetic mean; vertical lines extend from the box to a distance of at most 1.5 IQRs; percentages refer to change from baseline in arithmetic mean. Outliers are plotted separately. ANCOVA, analysis of covariance; CHEST-1, Chronic Thromboembolic Pulmonary Hypertension Soluble Guanylate Cyclase–Stimulator Trial 1;CTEPH, chronic thromboembolic pulmonary hypertension; LS, least-squares; PEA, pulmonary endarterectomy; PH, pulmonary hypertension.
Figure 2.
Boxplots for cardiac index at baseline (BL) and CHEST-1 week 16 in the overall population and the inoperable CTEPH and persistent/recurrent PH after PEA subgroups. LS mean treatment effect (95% CI) was determined using ANCOVA. Box: 25th to 75th percentile; horizontal line: median; cross: arithmetic mean; vertical lines extend from the box to a distance of at most 1.5 IQRs; percentages refer to change from baseline in arithmetic mean. Outliers are plotted separately. ANCOVA, analysis of covariance; CHEST-1, Chronic Thromboembolic Pulmonary Hypertension Soluble Guanylate Cyclase–Stimulator Trial 1; CTEPH, chronic thromboembolic pulmonary hypertension; LS, least-squares; PEA, pulmonary endarterectomy; PH, pulmonary hypertension.
The haemodynamic improvements with riociguat in the inoperable CTEPH and persistent/recurrent PH after PEA subgroups were largely consistent with the results from the overall population (table 2; figures 1 and 2). There were significant changes in PVR, SVR, mPAP, cardiac output, cardiac index, SvO2 and MAP in the inoperable CTEPH subgroup, while in the persistent/recurrent PH after PEA subgroup, there were significant changes in PVR, mPAP and MAP. Diastolic pulmonary artery pressure also improved at week 16 in both subgroups with riociguat compared with placebo (table 2). Improvements in PVR, cardiac output, cardiac index, mPAP and DPG were generally greater in the inoperable CTEPH subgroup than the persistent/recurrent PH after PEA subgroup (table 2; figures 1 and 2); however, the relative changes in these parameters in riociguat-treated patients were similar between the inoperable CTEPH subgroup and persistent/recurrent PH after PEA subgroup: cardiac output (+21% vs +18%, respectively), cardiac index (+21% vs +17%, respectively), mPAP (−9% vs −12%, respectively) and DPG (−19% vs −21%, respectively). An analysis of covariance for the interaction between change from baseline to week 16 in inoperable and persistent/recurrent subgroups showed significant differences in PVR, SVR and cardiac index (p=0.0089, 0.0080 and 0.0408, respectively; table 2).
Effect on other end points
Riociguat significantly improved the primary end point, change from baseline in 6MWD at week 16, in the overall population by an LS mean difference versus placebo of +46 m (95% CI 25 to 67 m; p<0.0001) (figure 2). The changes in 6MWD at week 16 were +54 m (95% CI 29 to 78 m) in the inoperable CTEPH subgroup and +26 m (95% CI −16 to 68 m) in the persistent/recurrent PH after PEA subgroup.
In the overall population, changes in 6MWD correlated weakly with changes in PVR (r=−0.29; 95% CI −0.41 to −0.17; p<0.0001) and cardiac index (r=0.23; 95% CI 0.10 to 0.35; p=0.0004) (figure 3). The correlation coefficient between 6MWD and PVR was −0.11 (95% CI −0.23 to 0.01; p=0.0795) at baseline and, for 6MWD versus cardiac index at baseline, it was 0.14 (95% CI 0.02 to 0.26; p=0.0226). The correlation coefficient between 6MWD and PVR was −0.20 (95% CI −0.32 to −0.07; p=0.0021) at week 16 and, for 6MWD versus cardiac index at week 16, it was 0.20 (95% CI 0.07 to 0.32; p=0.0020).
Figure 3.
Correlation scatter plots showing change from baseline to week 16 in (A) 6MWD and PVR and (B) 6MWD and cardiac index. Correlation was assessed using a Spearman's rank analysis. The line of best fit was determined using a linear regression analysis. 6MWD, 6 min walk distance; PVR, pulmonary vascular resistance.
Safety
Detailed safety data from the CHEST-1 study have been published previously.21 There were no differences in AEs between the inoperable and persistent/recurrent subgroups (table 3). AEs specific to the RHC procedure were infrequent; in the overall population, two patients (1%) in the riociguat group experienced an AE of catheter-site haemorrhage compared with no such events in the placebo group.
Table 3.
Adverse events occurring in more than 5% of patients in any group
| Adverse event, n (%) | Inoperable |
Persistent/recurrent PH following PEA |
||
|---|---|---|---|---|
| Riociguat (n=121) | Placebo (n=68) | Riociguat (n=52) | Placebo (n=20) | |
| Any | 108 (89) | 61 (90) | 51 (98) | 15 (75) |
| Dizziness | 27 (22) | 8 (12) | 12 (23) | 3 (15) |
| Headache | 26 (21) | 8 (12) | 17 (33) | 4 (20) |
| Dyspepsia | 20 (17) | 6 (9) | 11 (21) | 1 (5) |
| Peripheral oedema | 17 (14) | 15 (22) | 10 (19) | 3 (15) |
| Nasopharyngitis | 14 (12) | 6 (9) | 12 (23) | 2 (10) |
| Hypotension | 13 (11) | 3 (4) | 3 (6) | 0 |
| Diarrhoea | 11 (9) | 3 (4) | 6 (12) | 1 (5) |
| Nausea | 9 (7) | 6 (9) | 10 (19) | 1 (5) |
| Upper respiratory tract infection | 9 (7) | 3 (4) | 1 (2) | 1 (5) |
| Vomiting | 8 (7) | 2 (3) | 9 (17) | 1 (5) |
| Increased INR | 8 (7) | 4 (6) | 2 (4) | 0 |
| Prolonged aPTT | 7 (6) | 2 (3) | 1 (2) | 0 |
| Cough | 6 (5) | 11 (16) | 3 (6) | 5 (25) |
| Dyspnoea | 6 (5) | 9 (13) | 2 (4) | 3 (15) |
| Urinary tract infection | 6 (5) | 0 | 1 (2) | 2 (10) |
| Abdominal discomfort | 6 (5) | 0 | 0 | 2 (10) |
| Back pain | 5 (4) | 5 (7) | 2 (4) | 0 |
| Chest pain | 5 (4) | 4 (6) | 2 (4) | 0 |
| Flushing | 4 (3) | 2 (3) | 3 (6) | 0 |
| Gastro-oesophageal reflux disease | 4 (3) | 0 | 3 (6) | 0 |
| Hypokalaemia | 3 (2) | 2 (3) | 4 (8) | 0 |
| Extremity pain | 3 (2) | 5 (7) | 0 | 0 |
| Hyperkalaemia | 3 (2) | 0 | 0 | 2 (10) |
| Palpitations | 2 (2) | 2 (3) | 4 (8) | 2 (10) |
| Insomnia | 2 (2) | 5 (7) | 2 (4) | 1 (5) |
| Muscle spasms | 1 (1) | 2 (3) | 3 (6) | 0 |
| Respiratory tract infection | 1 (1) | 0 | 3 (6) | 1 (5) |
| Hyperhidrosis | 1 (1) | 2 (3) | 0 | 2 (10) |
| Increased blood creatinine | 0 | 4 (6) | 3 (6) | 1 (5) |
| Oropharyngeal pain | 0 | 0 | 3 (6) | 0 |
aPTT, activated partial thromboplastin time; INR, international normalised ratio; PEA, pulmonary endarterectomy; PH, pulmonary hypertension.
Discussion
In the Phase III CHEST-1 study, riociguat significantly improved a range of haemodynamic variables in patients with CTEPH, including PVR, mPAP, cardiac index and SvO2. These haemodynamic improvements were generally observed in both patients with inoperable CTEPH and those with persistent/recurrent PH after PEA. In the overall study population, a small yet significant correlation was observed between the change in 6MWD and the change in haemodynamic variables (PVR and cardiac index). These results complement the primary end point of improvements in exercise capacity with riociguat in the CHEST-1 study, together with improvements in a range of secondary end points including NT-proBNP and WHO functional class.21
To date, the CHEST-1 study represents the largest and most detailed haemodynamic characterisation of patients with inoperable CTEPH or persistent/recurrent PH after PEA at baseline and after targeted therapy. The improvements in PVR, mPAP, cardiac index and SvO2 in the overall population were observed without relevant changes in heart rate and were largely consistent in patients with inoperable CTEPH and those with persistent/recurrent PH after PEA. Patients in the persistent/recurrent PH after PEA subgroup of CHEST-1 showed numerically lower improvements from baseline to week 16; however, they had a lower PVR and higher 6MWD at baseline compared with patients in the inoperable subgroup. Nevertheless, the relative changes in PVR, mPAP, cardiac index and SvO2 were comparable between the two subgroups and 6MWD increased to similar levels between the two subgroups (379 m and 387 m in patients with inoperable and persistent/recurrent PH after PEA, respectively).
Haemodynamic parameters are objective indicators of the status of the pulmonary circulation, with reports indicating that PVR, mPAP, RAP and cardiac index are predictive of outcome in patients with CTEPH.11 24 25 Whether the acute effects of riociguat on haemodynamics translate into long-term benefits for patients with inoperable CTEPH or persistent/recurrent PH following PEA is unknown. Currently, the long-term extension study CHEST-2 is actively monitoring safety and durability of clinical parameters over an extended period beyond the original 16 weeks of the CHEST-1 study.26
The broader impact of haemodynamic improvements with riociguat requires further characterisation. In the primary analysis of the CHEST-1 study, the changes in PVR, mPAP, SvO2 and cardiac index were accompanied by a significant decrease in NT-proBNP,21 which has been shown to be a biomarker of RV function and an indicator of prognosis.8 Furthermore, haemodynamic improvements correlated with improvements in 6MWD in the present analysis. These complementary data demonstrate the value of measuring improvements across multiple parameters in order to more fully evaluate disease severity and better understand the effect of a given treatment.
Riociguat demonstrated efficacy in both 6MWD and PVR in patients with CTEPH. Previous trials of PAH-targeted therapies for the treatment of patients with CTEPH have had variable results.15 16 PEA is still the recommended therapy for patients with operable CTEPH as it represents the only potentially curative option.6 7 Therefore, all patients with suspected CTEPH should always be referred to an expert centre for confirmation of diagnosis, assessment of operability and surgical treatment if deemed eligible.6 7 However, 20%–40% of patients with CTEPH may be considered inoperable or have persistent/recurrent CTEPH after PEA and are candidates for medical treatment.6 7 27
Limitations
There were several limitations in the CHEST-1 study. Although the analyses of the inoperable CTEPH and persistent/recurrent PH after PEA subgroups were pre-specified, statistical testing of the haemodynamic data in these subgroups was performed post hoc, although using the same statistical methods as the pre-specified subgroup analyses for 6MWD. Moreover, the CHEST-1 study was not powered to detect statistically significant differences in subgroups. The data presented are for 16 weeks of riociguat therapy and long-term haemodynamic measurements were not planned. Therefore, future studies will need to determine if the haemodynamic changes at week 16 correlate with long-term clinical outcome.
Conclusion
In summary, riociguat improved a range of haemodynamic variables in both patients with inoperable CTEPH and patients with persistent/recurrent PH after PEA in CHEST-1 and improvements were comparable between the subgroups. In the overall population, improvements in PVR and cardiac index correlated with increases in 6MWD. These results emphasise the efficacy of riociguat in the CHEST-1 study, adding to the previously reported improvements in exercise capacity and other clinically relevant parameters.
Key messages.
What is already known on this subject?
In the Chronic Thromboembolic Pulmonary Hypertension Soluble Guanylate Cyclase–Stimulator Trial 1 (CHEST-1) study, treatment with riociguat significantly improved exercise capacity and a range of clinically relevant end points in patients with chronic thromboembolic pulmonary hypertension (CTEPH).
What might this study add?
This study adds a detailed comparison of the haemodynamic data from the inoperable and persistent/recurrent CTEPH subgroups in CHEST-1. Riociguat decreased pulmonary vascular resistance (PVR) in inoperable (least-squares mean difference: −285 dyn s/cm5; p<0.0001) and persistent/recurrent (−131 dyn s/cm5; p=0.0025) patients and improved several other haemodynamic parameters. Overall, changes in 6 min walk distance correlated with changes in PVR and cardiac index.
How might this impact on clinical practice?
Taken together with the results of the CHEST-1 study, these data confirm the beneficial haemodynamic effects of riociguat in patients with inoperable and persistent/recurrent CTEPH and demonstrate the value of measuring improvements across multiple parameters to better understand the effects of treatment.
Footnotes
Contributors: NHK takes overall responsibility for all aspects of the reliability and freedom from bias of the data presented and their discussed interpretation. NHK, FG, MMH, EM, GS and H-AG were members of the CHEST-1 steering committee and as such contributed to the conception and design of the CHEST-1 study. NHK, AMD'A, FG, EG, MMH, PJ, EM, CN, GS, AT, CW and H-AG recruited and treated patients in the CHEST-1 study. AF performed the statistical analysis. NHK, AMD'A, FG, EG, MMH, PJ, EM, CN, GS,AT,CW, AF, ND and H-AG contributed to the conception and design of this paper, the analysis and interpretation of the data and the drafting, critical review and approval of the final manuscript.
Collaborators: Full list of CHEST-1 investigators: Argentina: E Perna, Australia: T Williams, Austria: I Lang and C Kaehler, Belgium: M Delcroix and J-L Vachiery, Brazil: J Arakaki, D Waetge and G Meyer, Canada: J Granton, A Hirsch, D Helmersen, S Mehta and L Mielniczuk, China: Z Liu, C Wang, Z Cheng, Z Jing and L Pan, Czech Republic: P Jansa, Denmark: J-E Nielsen-Kudsk, France: G Simonneau, I Franchon, A Chaouat, P De Groote, E Bergot, F Bauer, C Dromer and C-H Marquette, Germany: H-A Ghofrani, M Hoeper, C Neurohr, H Wilkens, G Hoffken, S Rosenkranz, H Wirtz, R Ewert, E Grünig, H Klose, A Filusch and M Held, Italy: AM D'Armini and M Morsolini, Japan: Y Fukumoto, N Tanabe, M Sano, M Hatano, Y Takeda, M Sakuma, T Higo, T Satoh, M Ohe, M Owa, O Okazaki, M Ajioka, M Iwabuchi, M Takata and Y Akashi, Netherlands: A Boonstra, Mexico: C Sanchez Diaz, U Martinez, M Gamba and T Pulido Zamudio, Poland: A Torbicki and P Podolec, Portugal: G Castro, Republic of Korea: S Lee and H Kim, Russia: O Moiseeva and A Chernyavsky, Slovakia: I Simkova, Spain: MA Gomez Sanchez and JA Barbera, Switzerland: R Speich, Taiwan: Y-H Lin, Turkey: G Karabiyikoglu, N Mogulkoc and G Okumus, UK: J Pepke-Zaba, A Peacock and L Howard, USA: R Allen, N Sood, S Chaparro, F Torres, G Heresi, A Zaiman, K Kerr, H Farber and S Hansdottir.
Funding: This study was funded by Bayer Pharma AG (Berlin, Germany). Editorial assistance was provided by Adelphi Communications (Bollington, UK), sponsored by Bayer Pharma AG.
Competing interests: NHK reports personal fees and non-financial support from Bayer HealthCare Pharmaceuticals; grants and personal fees from Actelion; grants from Gilead, Lung LLC and United Therapeutics. AMD'A reports personal fees from Bayer HealthCare Pharmaceuticals and personal fees from Actelion. FG reports grants, personal fees and non-financial support from Bayer HealthCare Pharmaceuticals and personal fees from Actelion, Lilly, Novartis and Pfizer. EG reports grants, personal fees and non-financial support from Bayer HealthCare Pharmaceuticals, grants and personal fees from Actelion, GSK, Lilly and Pfizer, non-financial support from Alexion and personal fees from Miltenyi, Novartis and United Therapeutics. MMH reports grants, personal fees and non-financial support from Bayer HealthCare Pharmaceuticals and personal fees from Actelion, GSK, Lilly, Novartis and Pfizer. PJ, an investigator for Actelion, reports grants, personal fees and non-financial support from Bayer HealthCare Pharmaceuticals and personal fees from AOP. EM reports personal fees and non-financial support from Bayer HealthCare Pharmaceuticals and personal fees from Actelion, GSK and Pfizer. CN reports grants, personal fees and non-financial support from Bayer HealthCare Pharmaceuticals and personal fees from Actelion, GSK, Novartis and Pfizer. GS reports grants, personal fees and non-financial support from Bayer HealthCare Pharmaceuticals, Actelion, GSK, Lilly and Pfizer and personal fees and non-financial support from Novartis. AT reports grants, personal fees and non-financial support from Bayer HealthCare Pharmaceuticals and grants and personal fees from Actelion, GSK and AOP. CW has nothing to report. AF is an employee of Bayer Pharma AG. ND is an employee of Bayer Pharma AG. H-AG reports grants from Actelion, Bayer HealthCare Pharmaceuticals, Ergonex and Pfizer and personal fees from Actelion, Bayer HealthCare Pharmaceuticals, Ergonex, Gilead, GSK, Merck, Novartis and Pfizer.
Provenance and peer review: Not commissioned; externally peer reviewed.
Contributor Information
Collaborators: E Perna, T Williams, I Lang, C Kaehler, M Delcroix, J-L Vachiery, J Arakaki, D Waetge, G Meyer, J Granton, A Hirsch, D Helmersen, S Mehta, L Mielniczuk, Z Liu, Z Cheng, Z Jing, L Pan, J-E Nielsen-Kudsk, I Franchon, A Chaouat, P De Groote, E Bergot, F Bauer, C Dromer, C-H Marquette, H Wilkens, G Hoffken, S Rosenkranz, H Wirtz, R Ewert, H Klose, A Filusch, M Held, M Morsolini, Y Fukumoto, N Tanabe, M Sano, M Hatano, Y Takeda, M Sakuma, T Higo, T Satoh, M Ohe, M Owa, O Okazaki, M Ajioka, M Iwabuchi, M Takata, Y Akashi, A Boonstra, C Sanchez Diaz, U Martinez, M Gamba, T Pulido Zamudio, P Podolec, G Castro, S Lee, H Kim, O Moiseeva, A Chernyavsky, I Simkova, MA Gomez Sanchez, JA Barbera, R Speich, Y-H Lin, G Karabiyikoglu, N Mogulkoc, G Okumus, J Pepke-Zaba, A Peacock, L Howard, R Allen, N Sood, S Chaparro, F Torres, G Heresi, A Zaiman, K Kerr, H Farber, and S Hansdottir
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