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Effect of the P-Selectin Inhibitor Crizanlizumab on Survival Free of Organ Support in Patients Hospitalized for COVID-19: A Randomized Controlled Trial.
Solomon, Scott D; Lowenstein, Charles J; Bhatt, Ankeet S; Peikert, Alexander; Vardeny, Orly; Kosiborod, Mikhail N; Berger, Jeffrey S; Reynolds, Harmony R; Mavromichalis, Stephanie; Barytol, Anya; Althouse, Andrew D; Luther, James F; Leifer, Eric S; Kindzelski, Andrei L; Cushman, Mary; Gong, Michelle N; Kornblith, Lucy Z; Khatri, Pooja; Kim, Keri S; Baumann Kreuziger, Lisa; Wahid, Lana; Kirwan, Bridget-Anne; Geraci, Mark W; Neal, Matthew D; Hochman, Judith S.
Afiliação
  • Solomon SD; Cardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (S.D.S., A.S.B., A.P., A.B.).
  • Lowenstein CJ; Johns Hopkins School of Medicine, Baltimore, MD (C.J.L.).
  • Bhatt AS; Cardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (S.D.S., A.S.B., A.P., A.B.).
  • Peikert A; Kaiser Permanente San Francisco Medical Center, CA (A.S.B.).
  • Vardeny O; Cardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (S.D.S., A.S.B., A.P., A.B.).
  • Kosiborod MN; University of Minnesota and the Minneapolis VA Medical Center (O.V.).
  • Berger JS; Saint Luke's Mid America Heart Institute, University of Missouri-Kansas City (M.N.K.).
  • Reynolds HR; Cardiovascular Clinical Research Center, NYU Grossman School of Medicine, New York (J.S.B., H.R.R., S.M., J.S.H.).
  • Mavromichalis S; Cardiovascular Clinical Research Center, NYU Grossman School of Medicine, New York (J.S.B., H.R.R., S.M., J.S.H.).
  • Barytol A; Cardiovascular Clinical Research Center, NYU Grossman School of Medicine, New York (J.S.B., H.R.R., S.M., J.S.H.).
  • Althouse AD; Cardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (S.D.S., A.S.B., A.P., A.B.).
  • Luther JF; University of Pittsburgh, PA (A.D.A., J.F.L., M.W.G., M.D.N.).
  • Leifer ES; University of Pittsburgh, PA (A.D.A., J.F.L., M.W.G., M.D.N.).
  • Kindzelski AL; National Heart, Lung, and Blood Institute, Bethesda, MD (E.S.L., A.L.K.).
  • Cushman M; National Heart, Lung, and Blood Institute, Bethesda, MD (E.S.L., A.L.K.).
  • Gong MN; Larner College of Medicine, University of Vermont, Burlington (M.C.).
  • Kornblith LZ; Albert Einstein College of Medicine, Bronx, NY (M.N.G.).
  • Khatri P; University of California, San Francisco (L.Z.K.).
  • Kim KS; University of Cincinnati Medical Center, OH (P.K.).
  • Baumann Kreuziger L; University of Illinois, Chicago (K.S.K.).
  • Wahid L; Versity Blood Research Institute, Milwaukee, WI (L.B.K.).
  • Kirwan BA; Duke University, Durham, NC (L.W.).
  • Geraci MW; Socar Research SA, Nyon, Switzerland (B.-A.K.).
  • Neal MD; University of Pittsburgh, PA (A.D.A., J.F.L., M.W.G., M.D.N.).
  • Hochman JS; University of Pittsburgh, PA (A.D.A., J.F.L., M.W.G., M.D.N.).
Circulation ; 148(5): 381-390, 2023 08.
Article em En | MEDLINE | ID: mdl-37356038
ABSTRACT

BACKGROUND:

COVID-19 has been associated with endothelial injury, resultant microvascular inflammation and thrombosis. Activated endothelial cells release and express P-selectin and von Willebrand factor, both of which are elevated in severe COVID-19 and may be implicated in the disease pathophysiology. We hypothesized that crizanlizumab, a humanized monoclonal antibody to P-selectin, would reduce morbidity and death in patients hospitalized for COVID-19.

METHODS:

An international, adaptive, randomized controlled platform trial, funded by the National Heart, Lung, and Blood Institute, randomly assigned 422 patients hospitalized with COVID-19 with moderate or severe illness to receive either a single infusion of the P-selectin inhibitor crizanlizumab (at a dose of 5 mg/kg) plus standard of care or standard of care alone in an open-label 11 ratio. The primary outcome was organ support-free days, evaluated on an ordinal scale consisting of the number of days alive free of organ support through the first 21 days after trial entry.

RESULTS:

The study was stopped for futility by the data safety monitoring committee. Among 421 randomized patients with known 21-day outcomes, 163 patients (77%) randomized to the crizanlizumab plus standard-of-care arm did not require any respiratory or cardiovascular organ support compared with 169 (80%) in the standard-of-care-alone arm. The adjusted odds ratio for the effect of crizanlizumab on organ support-free days was 0.70 (95% CI, 0.43-1.16), where an odds ratio >1 indicates treatment benefit, yielding a posterior probability of futility (odds ratio <1.2) of 98% and a posterior probability of inferiority (odds ratio <1.0) of 91%. Overall, there were 37 deaths (17.5%) in the crizanlizumab arm and 27 deaths (12.8%) in the standard-of-care arm (hazard ratio, 1.33 [95% CrI, 0.85-2.21]; [probability of hazard ratio>1] = 0.879).

CONCLUSIONS:

Crizanlizumab, a P-selectin inhibitor, did not result in improvement in organ support-free days in patients hospitalized with COVID-19. REGISTRATION URL https//www. CLINICALTRIALS gov; Unique identifier NCT04505774.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Circulation Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Circulation Ano de publicação: 2023 Tipo de documento: Article