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Pulmonary Hypertension and Anastrozole (PHANTOM): A Randomized, Double-Blind, Placebo-Controlled Trial.
Kawut, Steven M; Feng, Rui; Ellenberg, Susan S; Zamanian, Roham; Bull, Todd; Chakinala, Murali; Mathai, Stephen C; Hemnes, Anna; Lin, Grace; Doyle, Margaret; Andrew, Ruth; MacLean, Margaret; Stasinopoulos, Ioannis; Austin, Eric; DeMichele, Angela; Shou, Haochang; Minhas, Jasleen; Song, Nianfu; Moutchia, Jude; Ventetuolo, Corey E.
Afiliación
  • Kawut SM; University of Pennsylvania Perelman School of Medicine, 14640, Medicine , Philadelphia, Pennsylvania, United States; kawut@upenn.edu.
  • Feng R; University of Pennsylvania Perelman School of Medicine, 14640, Philadelphia, Pennsylvania, United States.
  • Ellenberg SS; Perelman School of Medicine, Philadelphia, Pennsylvania, United States.
  • Zamanian R; Stanford University Medical Center, Department of Medicine, Stanfod, California, United States.
  • Bull T; University of Colorado, 1878, Denver, Colorado, United States.
  • Chakinala M; Washington University in Saint Louis, 7548, Saint Louis, Missouri, United States.
  • Mathai SC; Johns Hopkins University School of Medicine, Division of Pulmonary and Critical Medicine, Baltimore, United States.
  • Hemnes A; Vanderbilt University Medical Center, 12328, Nashville, Tennessee, United States.
  • Lin G; Mayo Clinic Division of Cardiovascular Diseases, 172751, Rochester, Minnesota, United States.
  • Doyle M; University of Vermont College of Arts and Sciences, 173134, Burlington, Vermont, United States.
  • Andrew R; University of Edinburgh, Queen's Medical Research Institute, Edinburgh, United Kingdom of Great Britain and Northern Ireland.
  • MacLean M; University of Strathclyde, 3527, Glasgow, United Kingdom of Great Britain and Northern Ireland.
  • Stasinopoulos I; Strathclyde Institute of Pharmacy and Biomedical Sciences, 14306, Glasgow, United Kingdom of Great Britain and Northern Ireland.
  • Austin E; Vanderbilt University School of Medicine, Pediatrics, Pediatric Pulmonary Medicine, Nashville, Tennessee, United States.
  • DeMichele A; University of Pennsylvania, 6572, Philadelphia, Pennsylvania, United States.
  • Shou H; University of Pennsylvania, 6572, Department of Biostatistics, Epidemiology and Informatics, Philadelphia, Pennsylvania, United States.
  • Minhas J; University of Pennsylvania, 6572, Pulmonary, Allergy and Critical Care, Philadelphia, Pennsylvania, United States.
  • Song N; University of Pennsylvania, Department of Medicine, Philadelphia, Pennsylvania, United States.
  • Moutchia J; University of Pennsylvania, 6572, Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, United States.
  • Ventetuolo CE; Brown University, Medicine , Providence, Rhode Island, United States.
Article en En | MEDLINE | ID: mdl-38747680
ABSTRACT
RATIONALE Inhibition of aromatase with anastrozole reduces pulmonary hypertension in experimental models.

OBJECTIVES:

We aimed to determine whether anastrozole improved six-minute walk distance (6MWD) at six months in pulmonary arterial hypertension (PAH).

METHODS:

We performed a randomized, double-blind, placebo-controlled Phase II clinical trial of anastrozole in subjects with PAH at seven centers. Eighty-four post-menopausal women and men with PAH were randomized in a 11 ratio to receive anastrozole 1 mg or placebo by mouth daily, stratified by sex using permuted blocks of variable sizes. All subjects and study staff were masked. The primary outcome was the change from baseline in 6MWD at six months. Using intent-to-treat analysis, we estimated the treatment effect of anastrozole using linear regression models adjusted for sex and baseline 6MWD. Assuming 10% loss to follow-up, we anticipated having 80% power to detect a difference in the change in 6MWD of 22 meters. MEASUREMENTS AND MAIN

RESULTS:

Forty-one subjects were randomized to placebo and 43 to anastrozole and all received the allocated treatment. Three subjects in the placebo group and two in the anastrozole group discontinued study drug. There was no significant difference in the change in 6MWD at six months (placebo-corrected treatment effect -7.9 m, 95%CI -32.7 - 16.9, p = 0.53). There was no difference in adverse events between the groups.

CONCLUSIONS:

Anastrozole did not show a significant effect on 6MWD compared to placebo in post-menopausal women and men with PAH. Anastrozole was safe and did not show adverse effects. Clinical trial registration available at www. CLINICALTRIALS gov, ID NCT03229499.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2024 Tipo del documento: Article