News

Novel drug improved walk distance in pulmonary hypertension patients

View on the News

Scrutinize industry support

Riociguat "is poised for examination by the Food and Drug Administration as a therapy for pulmonary hypertension and, if approved, has the potential to generate substantial revenue" for the sponsor of these two clinical trials, said Dr. Stephen L. Archer.

Both CHEST-1 and PATENT-1 were sponsored by Bayer HealthCare, which also provided the statistician and editorial assistance for both trials. "In light of the financial stakes, both real and apparent investigator autonomy remain key to ensuring the delivery of new drugs for pulmonary hypertension for patients," he noted.

Although riociguat yielded only "modest" gains in exercise capacity, it looks promising and may prove to be the first effective oral therapy for inoperable Group 4 pulmonary hypertension, Dr. Archer added.

However, he noted limitations in both studies. The CHEST-1 trial was limited by its "failure to examine the effects of the study drug on the right ventricle. The 6-minute walk distance is as reflective of right ventricular or skeletal-muscle function as it is of reduction in pulmonary vascular resistance, the authors’ presumed mechanism of benefit."

PATENT-1 was limited by its modest effect size, he added. "This is particularly important, since 50% of the patients were receiving no other treatment for pulmonary arterial hypertension, and the rate of response to treatment among such patients is usually higher than the rate among patients who are receiving concomitant treatment for pulmonary arterial hypertension," Dr. Archer said.

Dr. Archer is in the department of medicine at Queen’s University, Kingston, Ont. He reported no financial conflicts of interest. These remarks were taken from his editorial accompanying Dr. Ghofrani’s reports (N. Engl. J. Med. 2013 July 25 [doi: 10.1056/NEJMe1306684]).


 

FROM THE NEW ENGLAND JOURNAL OF MEDICINE

These study subjects were randomly assigned to receive high-dose riociguat capped at 2.5 mg three times daily (254 patients), low-dose riociguat capped at 1.5 mg three times daily (63 patients), or placebo (126 patients) for 12 weeks. The analysis of data from the low-dose group was considered exploratory and was reported separately.

The primary endpoint – change from baseline in 6-minute walk distance – increased by a mean of 30 m in the high-dose group but decreased by a mean of 6 m in the placebo group in the intention-to-treat analysis. The results were similar in the per-protocol analysis, the investigators reported (N. Engl. J. Med. 2013 July 25 [doi: 10.1056/NEJMoa1209655]).

This treatment benefit was consistent across several subgroups of patients. In addition, the active drug significantly decreased pulmonary vascular resistance, improved mean pulmonary artery pressure and cardiac output, lengthened the interval to clinical worsening, improved NT-proBNP levels, improved WHO functional class, and improved scores on the Borg dyspnea scale.

In exploratory analyses, riociguat did not improve scores on one measure of QOL but did so on a disease-specific QOL tool.

Drug-related serious adverse events occurred in 1.4 % of patients receiving high-dose riociguat and 1% of those receiving placebo. A total of 3% of patients in the riociguat group and 7% of those in the placebo group discontinued the study drug because of adverse events.

Serious or drug-related adverse events in both groups included increased hepatic enzyme levels, acute renal failure, syncope, esophageal pain and swelling, supraventricular tachycardia, hypotension, generalized edema, hypoxemia, dyspnea, and worsening of pulmonary hypertension. There were two deaths in the riociguat group and three in the placebo group, none of which were considered to be related to the study drug.

A total of 396 of the subjects in the PATENT-1 study elected to enroll in an extended study of the long-term safety and efficacy of riociguat (the PATENT-2 clinical trial). An exploratory analysis of data from the first 12 weeks of that study showed a further mean increase of 53 m in 6-minute walk distance with high-dose riociguat.

CHEST-1 and PATENT-1 were funded by Bayer HealthCare. Dr. Ghofrani reported ties to Actelion, Bayer, and other companies. His associates reported ties to numerous industry sources.

Pages

Recommended Reading

Single-chamber ICDs better when pacing isn't required
MDedge Cardiology
IOM: Cut daily sodium, but not below 2,300 mg
MDedge Cardiology
Type 2 diabetics often harbor undiagnosed heart failure
MDedge Cardiology
Biventricular pacing bests conventional tx in BLOCK HF trial
MDedge Cardiology
Wearable defibrillator vest useful as bridge to ICD
MDedge Cardiology
Heart failure guidelines: New hope in medical therapy
MDedge Cardiology
Shock-Less trial improves physicians' ICD programming
MDedge Cardiology
Hospital revenue generated by cardiologists continues to drop
MDedge Cardiology
Cardiac rehabilitation benefits elderly heart failure patients
MDedge Cardiology
Copeptin helped differential diagnosis of hyponatremia
MDedge Cardiology