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Randomized Controlled Trial
. 2017 Feb 1;195(3):360-368.
doi: 10.1164/rccm.201605-1024OC.

Anastrozole in Pulmonary Arterial Hypertension. A Randomized, Double-Blind, Placebo-controlled Trial

Affiliations
Randomized Controlled Trial

Anastrozole in Pulmonary Arterial Hypertension. A Randomized, Double-Blind, Placebo-controlled Trial

Steven M Kawut et al. Am J Respir Crit Care Med. .

Abstract

Rationale: The aromatase inhibitor anastrozole blocks the conversion of androgens to estrogen and blunts pulmonary hypertension in animals, but its efficacy in treating patients with pulmonary arterial hypertension (PAH) is unknown.

Objectives: We aimed to determine the safety and efficacy of anastrozole in PAH.

Methods: We performed a randomized, double-blind, placebo-controlled trial of anastrozole in patients with PAH who received background therapy at two centers.

Measurements and main results: A total of 18 patients with PAH were randomized to anastrozole 1 mg or matching placebo in a 2:1 ratio. The two co-primary outcomes were percent change from baseline in 17β-estradiol levels (E2) and tricuspid annular plane systolic excursion (TAPSE) at 3 months. Anastrozole significantly reduced E2 levels compared with placebo (percent change: -40%; interquartile range [IQR], -61 to -26% vs. -4%; IQR, -14 to +4%; P = 0.003), but there was no difference in TAPSE. Anastrozole significantly increased the 6-minute-walk distance (median change = +26 m) compared with placebo (median change = -12 m) (median percent change: anastrozole group, 8%; IQR, 2 to 17% vs. placebo -2%; IQR, -7 to +1%; P = 0.042). Anastrozole had no effect on circulating biomarkers, functional class, or health-related quality of life. There was no difference in adverse events.

Conclusions: Anastrozole significantly reduced E2 levels in patients with PAH but had no effect on TAPSE. Anastrozole was safe, well tolerated, and improved 6-minute-walk distance in this small "proof-of-principle" study. Larger and longer phase II clinical trials of anastrozole may be warranted in patients with PAH. Clinical trial registered with www.clinicaltrials.gov (NCT 1545336).

Trial registration: ClinicalTrials.gov NCT01545336.

Keywords: anastrozole; clinical trial; pulmonary hypertension; sex hormones.

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Figures

Figure 1.
Figure 1.
Flow diagram. PAH = pulmonary arterial hypertension; 6WMT = 6-minute-walk test.
Figure 2.
Figure 2.
Percent change from baseline in serum estradiol levels at 6 weeks and 3 months in subjects receiving anastrozole (red) versus placebo (blue).
Figure 3.
Figure 3.
Percent change from baseline in tricuspid annular plane systolic excursion (TAPSE) at 3 months in subjects receiving anastrozole (red) versus placebo (blue).
Figure 4.
Figure 4.
Absolute change from baseline in 6-minute-walk distance (6MWD) at 6 weeks and 3 months in subjects receiving anastrozole (red) versus placebo (blue).
Figure 5.
Figure 5.
Percent change from baseline in N-terminal of the prohormone brain natriuretic peptide (NT-proBNP) at 6 weeks and 3 months in subjects receiving anastrozole (red) versus placebo (blue).

Comment in

References

    1. Dresdale DT, Schultz M, Michtom RJ. Primary pulmonary hypertension. I. Clinical and hemodynamic study. Am J Med. 1951;11:686–705. - PubMed
    1. Humbert M, Sitbon O, Chaouat A, Bertocchi M, Habib G, Gressin V, Yaïci A, Weitzenblum E, Cordier J-F, Chabot F, et al. Survival in patients with idiopathic, familial, and anorexigen-associated pulmonary arterial hypertension in the modern management era. Circulation. 2010;122:156–163. - PubMed
    1. Jacobs W, van de Veerdonk MC, Trip P, de Man F, Heymans MW, Marcus JT, Kawut SM, Bogaard HJ, Boonstra A, Vonk Noordegraaf A. The right ventricle explains sex differences in survival in idiopathic pulmonary arterial hypertension. Chest. 2014;145:1230–1236. - PMC - PubMed
    1. Kawut SM, Al-Naamani N, Agerstrand C, Rosenzweig EB, Rowan C, Barst RJ, Bergmann S, Horn EM. Determinants of right ventricular ejection fraction in pulmonary arterial hypertension. Chest. 2009;135:752–759. - PMC - PubMed
    1. Benza RL, Miller DP, Gomberg-Maitland M, Frantz RP, Foreman AJ, Coffey CS, Frost A, Barst RJ, Badesch DB, Elliott CG, et al. Predicting survival in pulmonary arterial hypertension: insights from the Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management (REVEAL) Circulation. 2010;122:164–172. - PubMed

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