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Phase I dose escalation study of bortezomib in combination with lenalidomide in patients with myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML)
Authors:Eyal C. Attar  Philip C. Amrein  James W. Fraser  Amir T. Fathi  Steven McAfee  Martha Wadleigh  Daniel J. DeAngelo  David P. Steensma  Richard M. Stone  Julia Foster  Donna Neuberg  Karen K. Ballen
Affiliation:1. Center for Leukemia, Massachusetts General Hospital Cancer Center, Boston, MA, USA;2. Adult Leukemia Program, Dana-Farber Cancer Institute, Boston, MA, USA;3. Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA
Abstract:We conducted a phase I dose escalation study to determine the maximal tolerated dose of bortezomib that could be combined with standard dose lenalidomide in patients with MDS or AML. Treatment consisted of bortezomib (IV) on Days 1, 4, 8, and 11 and lenalidomide 10 mg daily (PO) days 1–21 in 28 day cycles for up to 9 cycles. 23 patients (14 MDS/CMML, 9 AML) were enrolled. The maximally tested dose of bortezomib, 1.3 mg/m2, was tolerable in this regimen. Responses were seen in patients with MDS and AML. Further testing of this regimen is planned.
Keywords:Bortezomib and lenalidomide in MDS and AML
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