Proteus Syndrome

Biesecker, Leslie G.

doi:10.1002/9780470893159.ch43

Cited by 2 publications

(1 citation statement)

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“…4 The p.Glu17Lys variant activates this kinase, leading to the pathology of Proteus syndrome. While some symptomatic management strategies have been developed, 5,6 there is no primary treatment.…”

Section: Introductionmentioning

confidence: 99%

Pharmacodynamic Study of Miransertib in Individuals with Proteus Syndrome

Keppler‐Noreuil

Sapp

Lindhurst

et al. 2019

The American Journal of Human Genetics

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Proteus syndrome is a life-threatening segmental overgrowth syndrome caused by a mosaic gain-of-function AKT1 variant. There are no effective treatments for Proteus syndrome. Miransertib is an AKT1 inhibitor that, prior to this study, has been evaluated only in adult oncology trials. We designed a non-randomized, phase 0/1 pilot study of miransertib in adults and children with Proteus syndrome to identify an appropriate dosage starting point for a future efficacy trial using a pharmacodynamic endpoint. The primary endpoint was a 50% reduction in the tissue levels of AKT phosphorylation from biopsies in affected individuals. We also evaluated secondary efficacy endpoints. We found that a dose of 5 mg/m 2 /day (1/7 the typical dose used in oncology) led to a 50% reduction in phosphorylated AKT (pAKT) in affected tissues from five of six individuals. This dose was well tolerated. Two of the six efficacy endpoints (secondary objectives) suggested that this agent may be efficacious. We observed a decrease in a cerebriform connective tissue nevus and a reduction in pain in children. We conclude that 5 mg/m 2 /day of miransertib is an appropriate starting point for future efficacy trials and that this agent shows promise of therapeutic efficacy in children with Proteus syndrome.

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Section: Introductionmentioning

confidence: 99%