Experimental Biology and Medicine >
Volume 231, Number 6 >
Pp. 696-699
Clinical Pharmacology Unit, Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, Edinburgh, UK
1 Clinical Pharmacology Unit, Centre for Cardiovascular Science, University of Edinburgh, Queen’s Medical Research Institute, 3rd Floor East Room E3.22, 47 Little France Crescent, Edinburgh, EH16 4TJ, UK. E-mail: d.j.webb{at}ed.ac.uk
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Keywords: endothelin antagonists, heart failure, clinical trials
| The Role of Endothelin in Chronic Heart Failure |
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Similar to several other neurohumoral systems, the ET system is activated in chronic heart failure (CHF). In initial studies using animal models of experimental heart failure, treatment with either mixed or ETA selective antagonists significantly ameliorated left ventricular dysfunction, prevented ventricular remodeling, and prolonged survival after coronary artery ligation (2). Selective ETB antagonists, however, increased pulmonary and diastolic pressures and reduced cardiac output (3).
Plasma ET-1 concentrations in patients with CHF are correlated with both morbidity and mortality, prompting investigators to pursue the therapeutic potential of ET blockade in CHF (2). Investigators have examined the short-term hemodynamic effect of ET antagonists in patients with CHF. Two weeks of oral treatment with the mixed ET antagonist, bosentan, reduced pulmonary vascular resistance by approximately 40% and systemic vascular resistance by 30%, with no change in heart rate (4). Acute treatment with sitaxsentan, a selective ETA blocker, however, seemed to have a preferential effect on the pulmonary circulation; acute administration resulting in significant decreases in pulmonary artery systolic pressure and pulmonary vascular resistance but no effect on systemic hemodynamics (5).
In the light of such encouraging results, clinical trials were swiftly organized. In the Research on Endothelin Antagonists in Chronic Heart Failure (REACH-1) study (6), the long-term effects of the mixed ET antagonist, bosentan, (n = 244) versus placebo (n = 126) in patients with CHF (New York Heart Association [NYHA] Class IIIB/IV) were assessed. This trial was halted prematurely because of an increased incidence of elevated liver transaminase levels. At the time that the trial was stopped, however, patients who had been maintained on therapy during a 6-month period demonstrated a trend toward a reduced risk of heart failure–related mortality and morbidity. The possibility that long-term bosentan therapy at a lower dose would improve the clinical course of heart failure patients was evaluated in two companion large-scale clinical trials, Endothelin Antagonist Bosentan for Lowering Cardiac Events in Heart Failure (ENABLE) 1 and 2, which were conducted in the United States and Europe, respectively. Eight hundred and five patients with NYHA Class IIIB/IV CHF administered bosentan were compared with 808 patients treated with placebo. However, the results failed to demonstrate that the addition of bosentan to standard treatment reduced either morbidity or mortality (7). Treatment of 419 patients (Class II/III CHF) randomized to another mixed antagonist, enrasentan, or placebo failed to show benefit in a composite end point, including NYHA Class, hospitalization rate, and global assessment, and, in fact, showed a trend in favor of placebo (Enrasentan Cooperative Randomized Evaluation [ENCOR] study) (8). None of these clinical trials have been fully published and subjected to external peer review. Therefore, the effects of treatment with ET antagonists in CHF have not been released into the public domain, and there has been no opportunity to look across the trials to see whether there are subpopulations that might benefit, or to examine other aspects of these studies (such as plasma ET-1 concentrations).
In the Endothelin A Receptor Antagonist Trial in Heart Failure (EARTH) study, 642 patients with NYHA Class II–IV CHF were randomized to treatment either with darusentan or placebo during 24 weeks (9). The primary end point was the change in left ventricular end systolic volume (LVESV) measured by magnetic resonance imaging. No significant difference was seen in LVESV from values after placebo treatment for any dose of darusentan. Furthermore, there were no differences seen in terms of mortality or the progression of heart failure. Plasma concentrations of ET-1 increased dose-dependently in all groups receiving darusentan (P = 0.0028).
| Why Did the Clinical Trials Yield Negative Results? |
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First, although, for some drugs, such as angiotensin-converting enzyme (ACE) inhibitors, acute improvement of hemodynamic parameters in CHF patients can translate into reduced morbidity and mortality when used during a longer term in clinical trials (10), this relationship does not stand for all therapeutic agents. For example, treatment with inotropic agents improves the cardiac index of CHF patients when given acutely, but long-term administration to patients with advanced CHF increases mortality (11). The same may hold for ET antagonists; although they clearly improve cardiac output acutely, all clinical trials to date indicate that ET antagonists do not reduce morbidity or increase survival with long-term administration.
Second, although early studies using ET antagonists demonstrated improvements in hemodynamic variables and mortality in animal models of CHF after myocardial infarction (12, 13), thought to be caused by their action on cardiac remodeling, a recent meta-analysis of numerous preclinical studies has shown that ET antagonists have no net beneficial effect on mortality (14). It has been demonstrated that the early administration of ET antagonists after myocardial infarction resulted in increased mortality, most likely because of a remodeling-related increase in cardiac dimensions (15, 16).
Third, ET blockade might have been successful in the treatment of CHF if it had been introduced before the use of ACE inhibitors, β-blockers, and spironolactone, which are now established as standard CHF therapies. Once two neurohumoral systems are blocked, inhibition of a third system may provide little additional benefit, or the benefit may not be sufficient to be observed in the relatively small clinical trials performed to date. Nevertheless, it seems unlikely that such small benefits, in the global population of patients with NYHA III/IV CHF, will be clinically meaningful or cost-effective.
Fourth, there may be specific patient groups within the total population of CHF patients in which ET blockade is beneficial. ET antagonists are known to reduce pulmonary artery pressures in both patients with primary pulmonary hypertension and secondary pulmonary hypertension caused by left ventricular dysfunction (17, 18). Perhaps, if only CHF patients with raised pulmonary arterial pressures had been included, a clear benefit of treatment with ET antagonists would have emerged.
Finally, the benefits of ET blockade in CHF may derive from a truly ETA-selective approach. In CHF patients, ETA-selective antagonism, with BQ-123, reduced systemic vascular resistance and increased cardiac output compared with mixed ET blockade (18). In such patients, selective blockade of ETB, with BQ-788, had such a deleterious effect, causing systemic vasoconstriction and elevation of plasma ET-1 concentrations (19), that the authors withdrew this part of the study. In patients with chronic renal failure and hypertension, selective ETA blockade with BQ-123 reduced renal vascular resistance and increased natriuresis, effects not seen with mixed ETA and ETB receptor antagonism (20). Hence, selective ETA receptor antagonism might be more likely than the ETA/B blocking approach to avoid fluid retention in CHF patients. In the coronary microcirculation of patients with ischemic heart disease, endothelial dysfunction, a known independent risk factor for the development of cardiovascular disease (21), was improved after ETA, but not combined ETA/B, blockade (22).
All of the ET antagonists currently under clinical development are relatively ETA selective (Table 1). However, they are arbitrarily classified as ETA receptor antagonists if they demonstrate a more than 100-fold selectivity for the ETA over the ETB receptor (23). Both genetic knockout (24) and pharmacologic blockade of the ETB receptor in animals (25) and humans (26) results in elevated plasma ET-1 concentrations because of impaired clearance of ET-1. Administration of very high doses of relatively ETA-selective agents can result in ETB receptor blockade (27), causing increased ET-1 plasma concentrations. In contrast, there is no significant increase in ET-1 plasma concentrations after either acute ETA blockade with a range of doses of BQ-123 (19, 26, 28) or chronic ETA antagonism with ZD-4054 during 14 days (29). Raised plasma ET-1 concentrations, in the presence of an endothelin antagonist, can, therefore, be used as an index of ETB receptor binding by that drug.
The first three clinical trials of ET antagonists in CHF (REACH, ENABLE, and ENCOR) have not been published, therefore, their detailed results, including the effect of drug treatment on plasma ET-1 concentration, are not in the public domain. However, treatment with darusentan, the most ETA selective of the agents studied in CHF patients, resulted in a dose-dependent increase in plasma ET-1 concentrations in the EARTH study (9). Thus, we can conclude that the doses of ET antagonist used in this, and very likely in the other trials, did not offer truly ETA selective blockade.
| What Can Be Learned from the ET Antagonists in CHF Clinical Trials? |
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Although the EARTH study investigated the effect of an agent with modest selectivity for the ETA receptor in CHF, at the doses used in this trial it seems to have had significant activity at the ETB receptor. Truly ETA-selective ET antagonism, therefore, remains untested in these patients, although, sadly, reduced interest from the pharmaceutical industry in this area means that such a trial is unlikely to be organized in the near future.
Even if the consensus is that ET antagonists do not confer benefit in CHF, they are now licensed for the treatment of pulmonary hypertension and are being developed for other clinical applications in chronic renal disease, oncology, and the management of pain (30). We hope that valuable lessons, in terms of efficacy, toxicity, dosing, and receptor selectivity, can be learned and applied to these new clinical applications for ET antagonists.
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Received for publication September 29, 2005. Accepted for publication November 11, 2005.
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