Preclinical and clinical evaluation of Buparlisib (BKM120) in recurrent/refractory Central Nervous System Lymphoma.
Christian GrommesElena PentsovaLauren R SchaffCraig P NolanThomas J KaleyAnne S ReinerKatherine S PanageasIngo K MellinghoffPublished in: Leukemia & lymphoma (2023)
Central Nervous System (CNS) Lymphomas are aggressive brain tumors with limited treatment options. Targeting the phosphoinositide 3-kinase (PI3K) pathway yields promising responses across B-cell malignancies, but its therapeutic potential in CNS lymphomas remains unexplored. We present pre-clinical and clinical data on the pan-PI3K inhibitor Buparlisib in CNS lymphomas. In a primary CNS lymphoma-patient-derived cell line, we define the EC50. Four patients with recurrent CNS lymphoma were enrolled in a prospective trial. We evaluated Buparlisib plasma and cerebrospinal fluid pharmacokinetics, clinical outcomes, and adverse events. Treatment was well tolerated. Common toxicities include hyperglycemia, thrombocytopenia, and lymphopenia. The presence of Buparlisib in plasma and CSF was confirmed 2h post-treatment with a median CSF concentration below the EC50 defined in the cell line All four patients were evaluated for response and the median time to progression was 39 days. Buparlisib monotherapy did not lead to meaningful responses and the trial was prematurely stopped. Clinical Trial Registration: NCT02301364.
Keyphrases
- cerebrospinal fluid
- clinical trial
- blood brain barrier
- study protocol
- diffuse large b cell lymphoma
- phase iii
- phase ii
- end stage renal disease
- combination therapy
- ejection fraction
- newly diagnosed
- chronic kidney disease
- randomized controlled trial
- stem cells
- tyrosine kinase
- big data
- cell therapy
- electronic health record
- double blind