A phase II study of the AKT inhibitor TAS-117 in patients with advanced solid tumors and germline PTEN mutations
TAS-117 at the RP2D of 16 mg o.d. was tolerable, with a manageable safety profile. Clinical benefit, although durable, was only observed in a single patient with a germline PTEN mutation.
Authors
- T.W. Laetsch
- S.P. Chawla
- Y. He
- M. Mina
- A. Hervieu
- P. Funchain
- S. Delaloge
- H.-T. Arkenau
- V. Wacheck
- K. Anthony
- C.F. Singer
- Y.R. Murciano-Goroff
- J. Ródon
Institutions
- Twitter (United States) (US)
- Memorial Sloan Kettering Cancer Center (US)
- Children's Hospital of Philadelphia (US)
- The University of Texas MD Anderson Cancer Center (US)
- Sarah Cannon Research Institute (GB)
- Université Paris-Saclay (FR)
- Institut Gustave Roussy (FR)
- Comprehensive Cancer Center Vienna (AT)
- Centre Georges François Leclerc (FR)
- Sarcoma Oncology Center (US)
- Taiho Oncology (United States) (US)
- PTEN Hamartoma Tumor Syndrome Foundation (US)
- University of Pennsylvania (US)
Publication Details
- Journal
- ESMO Open
- Published
- 2025-12-30
- DOI
- https://doi.org/10.1016/j.esmoop.2025.105932
- Primary Topic
- PI3K/AKT/mTOR signaling in cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00