Lenalidomide is associated with increased risk of
thromboembolism (VTE) in patients with
multiple myeloma. This risk has not previously been defined in B-cell
non-Hodgkin lymphoma (NHL), for which
lenalidomide is also an active agent. We conducted a systematic literature search in Ovid MEDLINE (1946 to February 2017), Ovid EMBASE (1974 to February 2017), The Cochrane Library (Wiley), and Web of Science Core Collection for prospective studies evaluating
lenalidomide-containing regimens in B-cell NHL with adequate reporting of patient characteristics, total cycles received, and safety data including VTE rates. The primary outcome was VTE events per 100 patient-cycles by meta-analysis using random-effects models. Our literature search identified 1719 citations; 28 articles were included. For all patients with B-cell NHL receiving
lenalidomide, the rate of VTE per 100 patient-cycles was 0.77 (95% confidence interval [CI], 0.48-1.12; I2, 67%). The rate for single-agent
lenalidomide was 1.09 events per 100 patient-cycles (95% CI, 0.49-1.94; I2, 76%), the rate for
lenalidomide plus biologics was 0.49 (95% CI, 0.17-0.97; I2, 59%), and the rate for
lenalidomide plus
chemotherapy was 0.89 (95% CI, 0.39-1.60; I2, 57%). Rate of VTE events in B-cell NHL patients treated with
lenalidomide in clinical trials is similar to the rate in
multiple myeloma. The VTE rate appears to be lowest for
lenalidomide combined with a biologic compared with single-agent
lenalidomide or its combination with
chemotherapy. This protocol was registered at www.crd.york.ac.uk/prospero/ as #CRD42017056042.