| Literature DB >> 26139427 |
I M Ghobrial1, R Redd2, P Armand1, R Banwait1, E Boswell1, S Chuma1, D Huynh1, A Sacco1, A M Roccaro1, A Perilla-Glen1, K Noonan1, M MacNabb1, H Leblebjian1, D Warren1, P Henrick1, J J Castillo1, P G Richardson1, J Matous3, E Weller2, S P Treon1.
Abstract
We examined the combination of the mammalian target of rapamycin inhibitor everolimus with bortezomib and rituximab in patients with relapsed/refractory Waldenstrom macroglobulinemia (WM) in a phase I/II study. All patients received six cycles of the combination of everolimus/rituximab or everolimus/bortezomib/rituximab followed by maintenance with everolimus until progression. Forty-six patients were treated; 98% received prior rituximab and 57% received prior bortezomib. No dose-limiting toxicities were observed in the phase I. The most common treatment-related toxicities of all grades were fatigue (63%), anemia (54%), leucopenia (52%), neutropenia (48%) and diarrhea (43%). Thirty-six (78%) of the 46 patients received full dose therapy (FDT) of the three drugs. Of these 36, 2 (6%) had complete response (90% confidence interval (CI): 1-16). In all, 32/36 (89%) of patients experienced at least a minimal response (90% CI: 76-96%). The observed partial response or better response rate was 19/36 (53, 90 CI: 38-67%). For the 36 FDT patients, the median progression-free survival was 21 months (95% CI: 12-not estimable). In summary, this study demonstrates that the combination of everolimus, bortezomib and rituximab is well tolerated and achieved 89% response rate even in patients previously treated, making it a possible model of non-chemotherapeutic-based combination therapy in WM.Entities:
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Year: 2015 PMID: 26139427 DOI: 10.1038/leu.2015.164
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528