AI Article Synopsis

  • A female patient with multiple meningiomas in the lung underwent extensive treatment but continued tumor growth until an AKT1E17K mutation was found in her tumors.
  • The patient was treated with AZD5363, an AKT inhibitor, which led to stable disease and minor improvement, marking the first successful response to AKT inhibition in AKT1-mutant meningioma and highlighting the potential for molecular screening in patient treatment.

Article Abstract

High-throughput analyses have revealed the presence of activating mutations in the AKT1 gene in a subpopulation of meningiomas. We report a female patient with multiple intracranial tumor manifestations and histologically verified meningotheliomatous meningioma in the lung. The tumor was continuously growing at multiple sites despite six surgical resections, radiotherapy, and two lines of systemic therapy. Following detection of an AKT1E17K mutation in three independent tumor samples by sequencing, treatment with AZD5363, a selective AKT inhibitor, was initiated. Ex vivo cultured meningioma cells exhibited sensitivity to the drug as shown by pAKT accumulation on immunoblots. Treatment with AZD5363 resulted, for the first time, in stable disease and minor radiographic response. The patient has been on that treatment for more than one year with ongoing clinical and radiographic response. This is the first report of an AKT1-mutant meningioma responding to AKT inhibition, suggesting that molecular screening may result in clinical benefit.

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Source
http://dx.doi.org/10.1093/jnci/djw320DOI Listing

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