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Everolimus for renal angiomyolipoma in patients with tuberous sclerosis complex or sporadic lymphangioleiomyomatosis: extension of a randomized controlled trial
Author(s) -
John J. Bissler,
J.C. Kingswood,
Elżbieta Radzikowska,
Bernard A. Zonnenberg,
Michael Frost,
Е. Д. Белоусова,
Matthias Sauter,
Norio omura,
Susanne Brakemeier,
Petrus J. de Vries,
Noah Berkowitz,
Sara Miao,
Scott Segal,
Séverine Peyrard,
Klemens Budde
Publication year - 2015
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfv249
Subject(s) - tuberous sclerosis , medicine , everolimus , tolerability , lymphangioleiomyomatosis , angiomyolipoma , clinical endpoint , adverse effect , nephrology , target lesion , placebo , randomized controlled trial , urology , surgery , gastroenterology , kidney , radiology , pathology , alternative medicine , percutaneous coronary intervention , myocardial infarction
Mammalian target of rapamycin (mTOR) inhibitors are recommended as first-line treatment of renal angiomyolipoma associated with tuberous sclerosis complex (TSC) or sporadic lymphangioleiomyomatosis (sporadic LAM), but follow-up is limited. Longer term efficacy and tolerability data from a Phase 3, double-blind, placebo-controlled trial are presented.

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