| Literature DB >> 26659916 |
Meletios A Dimopoulos1, Matthew C Cheung2, Murielle Roussel3, Ting Liu4, Barbara Gamberi5, Brigitte Kolb6, H Guenter Derigs7, HyeonSeok Eom8, Karim Belhadj9, Pascal Lenain10, Richard Van der Jagt11, Sophie Rigaudeau12, Mamoun Dib13, Rachel Hall14, Henry Jardel15, Arnaud Jaccard16, Axel Tosikyan17, Lionel Karlin18, William Bensinger19, Rik Schots20, Nicolas Leupin21, Guang Chen21, Jennifer Marek21, Annette Ervin-Haynes21, Thierry Facon22.
Abstract
Renal impairment is associated with poor prognosis in myeloma. This analysis of the pivotal phase 3 FIRST trial examined the impact of renally adapted dosing of lenalidomide and dexamethasone on outcomes of patients with different degrees of renal impairment. Transplant-ineligible patients not requiring dialysis were randomized 1:1:1 to receive continuous lenalidomide and dexamethasone until disease progression (n=535) or for 18 cycles (72 weeks; n=541), or melphalan, prednisone, and thalidomide for 12 cycles (72 weeks; n=547). Follow-up is ongoing. Patients were grouped by baseline creatinine clearance into no (≥ 80 mL/min [n=389]), mild (≥ 50 to < 80 mL/min [n=715]), moderate (≥ 30 to < 50 mL/min [n=372]), and severe impairment (< 30 mL/min [n=147]) subgroups. Continuous lenalidomide and dexamethasone therapy reduced the risk of progression or death in no, mild, and moderate renal impairment subgroups vs. melphalan, prednisone, and thalidomide therapy (HR = 0.67, 0.70, and 0.65, respectively). Overall survival benefits were observed with continuous lenalidomide and dexamethasone treatment vs. melphalan, prednisone, and thalidomide treatment in no or mild renal impairment subgroups. Renal function improved from baseline in 52.6% of lenalidomide and dexamethasone-treated patients. The safety profile of continuous lenalidomide and dexamethasone was consistent across renal subgroups, except for grade 3/4 anemia and rash, which increased with increasing severity of renal impairment. Continuous lenalidomide and dexamethasone treatment, with renally adapted lenalidomide dosing, was effective for most transplant-ineligible patients with myeloma and renal impairment. Trial registration: ClinicalTrials.gov (NCT00689936); EudraCT (2007-004823-39). Funding: Intergroupe Francophone du Myélome and the Celgene Corporation. Copyright© Ferrata Storti Foundation.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26659916 PMCID: PMC4815728 DOI: 10.3324/haematol.2015.133629
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941