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Crizanlizumab and comparators for adults with sickle cell disease: a systematic review and network meta-analysis.
Thom, Howard; Jansen, Jeroen; Shafrin, Jason; Zhao, Lauren; Joseph, George; Cheng, Hung-Yuan; Gupta, Subhajit; Shah, Nirmish.
Afiliación
  • Thom H; Bristol Medical School, University of Bristol, Bristol, UK howard.thom@bristol.ac.uk.
  • Jansen J; Health Economics, PRECISIONheor, Los Angeles, California, USA.
  • Shafrin J; Health Economics, PRECISIONheor, Los Angeles, California, USA.
  • Zhao L; Health Economics, PRECISIONheor, Los Angeles, California, USA.
  • Joseph G; Novartis Pharmaceuticals Corp, East Hanover, New Jersey, USA.
  • Cheng HY; Bristol Medical School, University of Bristol, Bristol, UK.
  • Gupta S; Novartis Pharmaceuticals Corp, East Hanover, New Jersey, USA.
  • Shah N; Department of Medicine, Duke University, Durham, North Carolina, USA.
BMJ Open ; 10(9): e034147, 2020 09 17.
Article en En | MEDLINE | ID: mdl-32948541
ABSTRACT

OBJECTIVES:

Treatment options for preventing vaso-occlusive crises (VOC) among patients with sickle cell disease (SCD) are limited, especially if hydroxyurea treatment has failed or is contraindicated. A systematic literature review (SLR) and network meta-analysis (NMA) were conducted to evaluate the efficacy and safety of crizanlizumab for older adolescent and adult (≥16 years old) SCD patients.

METHODS:

The SLR included randomised controlled trials (RCTs) and uncontrolled studies. Bayesian NMA of VOC, all-cause hospitalisation days and adverse events were conducted.

RESULTS:

The SLR identified 51 studies and 9 RCTs on 14 treatments that met the NMA inclusion criteria. The NMA found that crizanlizumab 5.0 mg/kg was associated with a reduction in VOC (HR 0.55, 95% credible interval (0.43, 0.69); Bayesian probability of superiority >0.99), all-cause hospitalisation days (0.58 (0.50, 0.68); >0.99) and no evidence of difference on adverse events (0.91 (0.59, 1.43) 0.66) or serious adverse events (0.93 (0.47, 1.87); 0.59) compared with placebo. The HR for reduction in VOC for crizanlizumab relative to L-glutamine was (0.67 (0.50, 0.88); >0.99). These results were sensitive to assumptions regarding whether patient age is an effect modifier.

CONCLUSIONS:

This NMA provides preliminary evidence comparing the efficacy of crizanlizumab with other treatments for VOC prevention.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anemia de Células Falciformes Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Límite: Adult / Humans Idioma: En Revista: BMJ Open Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anemia de Células Falciformes Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Límite: Adult / Humans Idioma: En Revista: BMJ Open Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido
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