Geometry of the randomized evidence for treatments of pulmonary hypertension.

OBJECTIVE We studied the entire agenda of randomized clinical trials in pulmonary hypertension (PH) using sociological methods. We explored the geometry of the PH network to interpret the evidence on multiple competing treatments for the same indication. DESIGN We searched MEDLINE, Embase and Cochrane Library Databases for published studies. We queried clinicaltrials.gov and WHO International Clinical Trials Registry platform for non-published studies. RESULTS We found 75 randomized trials (41 published [n = 4136 participants] and 34 registered unpublished [planned n = 3470 participants]). Of the published randomized studies, all used placebo as the comparator arm except for two nonindustry-sponsored comparisons between phosphodiestearase-5 (PDE-5) inhibitors and endothelin receptor antagonists (ERA), and one study comparing two different regimens of treprostinil. Similarly, only five unpublished/ongoing trials used an active PH treatment as comparator (PDE-5 inhibitors versus ERA (n = 3), different doses of sildenafil (n = 1) and two formulations of epoprostenol (n = 1). Of the 75 trials, 47 were sponsored by the manufacturer of the tested active product(s), and only two trials were sponsored by two companies comparing their products. CONCLUSIONS The relative merits of different treatment options are not directly known, as there are very few head-to-head comparisons. A limited number of ongoing studies are using active FDA-approved PH-treatments for comparison. This lack of information can be overcome by carefully designing comparative effectiveness trials.

[1]  M. Gatzoulis,et al.  [Updated clinical classification of pulmonary hypertension]. , 2014, Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir.

[2]  John P A Ioannidis,et al.  Neglected tropical diseases: survey and geometry of randomised evidence , 2012, BMJ : British Medical Journal.

[3]  J. Ioannidis,et al.  Homophily and co-occurrence patterns shape randomized trials agendas: illustration in antifungal agents. , 2011, Journal of clinical epidemiology.

[4]  J. Ioannidis,et al.  The need to consider the wider agenda in systematic reviews and meta-analyses: breadth, timing, and depth of the evidence , 2010, BMJ : British Medical Journal.

[5]  A. Manes,et al.  A Randomized Open Label Study Comparing Bosentan To Sildenafil First-line Treatment In Pulmonary Arterial Hypertension And Chronic Thromboembolic Pulmonary Hypertension , 2010, ATS 2010.

[6]  L. Tavazzi,et al.  Systematic review of trials using vasodilators in pulmonary arterial hypertension: why a new approach is needed. , 2010, American heart journal.

[7]  J. Ioannidis,et al.  Industry sponsorship and selection of comparators in randomized clinical trials , 2010, European journal of clinical investigation.

[8]  H. Ghofrani,et al.  Updated evidence-based treatment algorithm in pulmonary arterial hypertension. , 2009, Journal of the American College of Cardiology.

[9]  B. Brundage,et al.  Tadalafil Therapy for Pulmonary Arterial Hypertension , 2009, Circulation.

[10]  A. Branzi,et al.  A meta-analysis of randomized controlled trials in pulmonary arterial hypertension , 2008, European heart journal.

[11]  Jeffrey L. Anderson,et al.  ACCF/AHA Expert Conseusus Document , 2009 .

[12]  M. Tamm,et al.  A randomised, controlled trial of bosentan in severe COPD , 2008, European Respiratory Journal.

[13]  S. Halpern,et al.  The ethics of randomized clinical trials in pulmonary arterial hypertension. , 2008, Proceedings of the American Thoracic Society.

[14]  B. Wiens,et al.  Ambrisentan for the Treatment of Pulmonary Arterial Hypertension: Results of the Ambrisentan in Pulmonary Arterial Hypertension, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Efficacy (ARIES) Study 1 and 2 , 2008, Circulation.

[15]  Georgia Salanti,et al.  Evaluation of networks of randomized trials , 2008, Statistical methods in medical research.

[16]  M. Christ-Crain,et al.  Use of B-type natriuretic peptide in the risk stratification of acute exacerbations of COPD. , 2008, Chest.

[17]  D. Asch,et al.  Physicians’ preferences for active-controlled versus placebo-controlled trials of new antihypertensive drugs , 2002, Journal of General Internal Medicine.

[18]  Stefan Leucht,et al.  Why olanzapine beats risperidone, risperidone beats quetiapine, and quetiapine beats olanzapine: an exploratory analysis of head-to-head comparison studies of second-generation antipsychotics. , 2006, The American journal of psychiatry.

[19]  M. Pillinger,et al.  Sildenafil Citrate Therapy for Pulmonary Arterial Hypertension , 2006 .

[20]  Deborah M Caldwell,et al.  Simultaneous comparison of multiple treatments: combining direct and indirect evidence , 2005, BMJ : British Medical Journal.

[21]  D. Pennell,et al.  Sildenafil versus Endothelin Receptor Antagonist for Pulmonary Hypertension (SERAPH) study. , 2005, American journal of respiratory and critical care medicine.

[22]  S. Rich,et al.  Continuous subcutaneous infusion of treprostinil, a prostacyclin analogue, in patients with pulmonary arterial hypertension: a double-blind, randomized, placebo-controlled trial. , 2002, American journal of respiratory and critical care medicine.

[23]  Orris,et al.  INHALED ILOPROST FOR SEVERE PULMONARY HYPERTENSION , 2002 .

[24]  Avid,et al.  BOSENTAN THERAPY FOR PULMONARY ARTERIAL HYPERTENSION , 2002 .

[25]  J. H. Diehl,et al.  Treatment of Primary Pulmonary Hypertension with Continuous Intravenous Prostacyclin (Epoprostenol): Results of a Randomized Trial , 1990 .