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Authordc.contributor.authorStelmaszewski, Erica V. 
Authordc.contributor.authorParente, Daniella B. 
Authordc.contributor.authorFariña, Alberto 
Authordc.contributor.authorStein, Anna 
Authordc.contributor.authorGutiérrez, Anthony 
Authordc.contributor.authorRaquelo Menegassio, Antonio F. 
Authordc.contributor.authorManterola, Carla 
Authordc.contributor.authorde Sousa, Carolina F. 
Authordc.contributor.authorVíctor, Carolina 
Authordc.contributor.authorMaki, Dina 
Authordc.contributor.authorMorón, Elías M. 
Authordc.contributor.authorde Abrantes, Fabiano F. 
Authordc.contributor.authorIqbal, Fátima 
Authordc.contributor.authorCamacho Vilchez, Jazmín 
Authordc.contributor.authorJiménez Pavón, Joanna 
Authordc.contributor.authorPolania, Juan P. 
Authordc.contributor.authorThompson, Lorenzo 
Authordc.contributor.authorBonanato, Lygia 
Authordc.contributor.authorDiebold, Matthias 
Authordc.contributor.authorDa Silva, Maria V. C. P. 
Authordc.contributor.authorNashwan, Mariam W. J. 
Authordc.contributor.authorGalvani, Marianna A. G. 
Authordc.contributor.authorIdris, Osama E. A. 
Authordc.contributor.authorDanos, Pierina 
Authordc.contributor.authorOrtiz López, Rocío 
Authordc.contributor.authorMahmoud, Rofida A. A. 
Authordc.contributor.authorGresse, Sergio Jr. 
Authordc.contributor.authorLoss, Karla L. 
Admission datedc.date.accessioned2020-06-23T23:21:49Z
Available datedc.date.available2020-06-23T23:21:49Z
Publication datedc.date.issued2020
Cita de ítemdc.identifier.citationCardiology in the Young Volumen: 30 Número: 3 Mar 2020es_ES
Identifierdc.identifier.other10.1017/S1047951119003147
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/175661
Abstractdc.description.abstractIntroduction: Tuberous sclerosis complex is a rare genetic disorder leading to the growth of hamartomas in multiple organs, including cardiac rhabdomyomas. Children with symptomatic cardiac rhabdomyoma require frequent admissions to intensive care units, have major complications, namely, arrhythmias, cardiac outflow tract obstruction and heart failure, affecting the quality of life and taking on high healthcare cost. Currently, there is no standard pharmacological treatment for this condition, and the management includes a conservative approach and supportive care. Everolimus has shown positive effects on subependymal giant cell astrocytomas, renal angiomyolipoma and refractory seizures associated with tuberous sclerosis complex. However, evidence supporting efficacy in symptomatic cardiac rhabdomyoma is limited to case reports. The ORACLE trial is the first randomised clinical trial assessing the efficacy of everolimus as a specific therapy for symptomatic cardiac rhabdomyoma. Methods: ORACLE is a phase II, prospective, randomised, placebo-controlled, double-blind, multicentre protocol trial. A total of 40 children with symptomatic cardiac rhabdomyoma secondary to tuberous sclerosis complex will be randomised to receive oral everolimus or placebo for 3 months. The primary outcome is 50% or more reduction in the tumour size related to baseline. As secondary outcomes we include the presence of arrhythmias, pericardial effusion, intracardiac obstruction, adverse events, progression of tumour reduction and effect on heart failure. Conclusions: ORACLE protocol addresses a relevant unmet need in children with tuberous sclerosis complex and cardiac rhabdomyoma. The results of the trial will potentially support the first evidence-based therapy for this condition.es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherCambridge University Presses_ES
Sourcedc.sourceCardiology in the Younges_ES
Keywordsdc.subjectEverolimuses_ES
Keywordsdc.subjectCardiac rhabdomyomaes_ES
Keywordsdc.subjectTuberous sclerosis complexes_ES
Keywordsdc.subjectChildrenes_ES
Títulodc.titleEverolimus for cardiac rhabdomyomas in children with tuberous sclerosis. The ORACLE study protocol (everOlimus for caRdiac rhAbdomyomas in tuberous sCLErosis): a randomised, multicentre, placebo-controlled, double-blind phase II triales_ES
Document typedc.typeArtículo de revistaes_ES
dcterms.accessRightsdcterms.accessRightsAcceso a solo metadatoses_ES
Catalogueruchile.catalogadorlajes_ES
Indexationuchile.indexArtículo de publicación ISI
Indexationuchile.indexArtículo de publicación SCOPUS


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