| Literature DB >> 27081177 |
Katja C Weisel1, Meletios A Dimopoulos2, Philippe Moreau3, Martha Q Lacy4, Kevin W Song5, Michel Delforge6, Lionel Karlin7, Hartmut Goldschmidt8, Anne Banos9, Albert Oriol10, Adrian Alegre11, Christine Chen12, Michele Cavo13, Laurent Garderet14, Valentina Ivanova15, Joaquin Martinez-Lopez16, Stefan Knop17, Xin Yu18, Kevin Hong18, Lars Sternas18, Christian Jacques18, Mohamed H Zaki18, Jesus San Miguel19.
Abstract
Pomalidomide + low-dose dexamethasone is effective and well tolerated for refractory or relapsed and refractory multiple myeloma after bortezomib and lenalidomide failure. The phase III trial MM-003 compared pomalidomide + low-dose dexamethasone with high-dose dexamethasone. This subanalysis grouped patients by baseline creatinine clearance ≥ 30 - < 60 mL/min (n=93, pomalidomide + low-dose dexamethasone; n=56, high-dose dexamethasone) or ≥ 60 mL/min (n=205, pomalidomide + low-dose dexamethasone; n=93, high-dose dexamethasone). Median progression-free survival was similar for both subgroups and favored pomalidomide + low-dose dexamethasone versus high-dose dexamethasone: 4.0 versus 1.9 months in the group with baseline creatinine clearance ≥ 30 - < 60 mL/min (P<0.001) and 4.0 versus 2.0 months in the group with baseline creatinine clearance ≥ 60 mL/min (P<0.001). Median overall survival for pomalidomide + low-dose dexamethasone versus high-dose dexamethasone was 10.4 versus 4.9 months (P=0.030) and 15.5 versus 9.2 months (P=0.133), respectively. Improved renal function, defined as an increase in creatinine clearance from < 60 to ≥ 60 mL/min, was similar in pomalidomide + low-dose dexamethasone and high-dose dexamethasone patients (42% and 47%, respectively). Improvement in progression-free and overall survival in these patients was comparable with that in patients without renal impairment. There was no increase in discontinuations of therapy, dose modifications, and adverse events in patients with moderate renal impairment. Pomalidomide at a starting dose of 4 mg + low-dose dexamethasone is well tolerated in patients with refractory or relapsed and refractory multiple myeloma, and of comparable efficacy if moderate renal impairment is present. This trial was registered with clinicaltrials.gov identifier 01311687 and EudraCT identifier 2010-019820-30. Copyright© Ferrata Storti Foundation.Entities:
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Year: 2016 PMID: 27081177 PMCID: PMC5004467 DOI: 10.3324/haematol.2015.137083
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941