The introduction of thalidomide, lenalidomide, and bortezomib has changed the way that multiple myeloma (MM) is treated and has greatly improved survival outcomes. These novel agents are often used in combination with conventional drugs, such as dexamethasone, to optimize clinical responses; however
Thromboembolic events with lenalidomide-based therapy for multiple myeloma
โ Scribed by Smitha Patiyil Menon; S. Vincent Rajkumar; Martha Lacy; Patrizia Falco; Antonio Palumbo
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 87 KB
- Volume
- 112
- Category
- Article
- ISSN
- 0008-543X
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โฆ Synopsis
Abstract
BACKGROUND.
The purpose was to evaluate the incidence and risk factors of thromboembolism associated with lenalidomide therapy in newly diagnosed myeloma.
METHODS.
A pooled analysis was performed of patients with previously untreated multiple myeloma enrolled in clinical trials of lenalidomideโbased therapy at the Mayo Clinic, Rochester, Minnesota, and the Italian Myeloma Network, Italy. The incidence of thrombosis, the effect of risk factors such as steroid dose and erythropoietin supplementation, and the effect of prophylaxis were examined.
RESULTS.
In all, 125 patients enrolled in 3 clinical trials were identified. Patients were stratified based on the concomitant corticosteroid dose. Fiftyโtwo patients were in the highโdose group (dexamethasone 40 mg, 12 days a month); 73 patients were in the lowโdose group (prednisone at any dose; or dexamethasone 40 mg, 4 days a month). A total of 110 patients were initiated on thromboprophylaxis; of these, 104 patients (95%) received aspirin. Ten patients (8%) developed deep vein thrombosis, including 4 who were not receiving any thromboprophylaxis at the time of the event. The rate of thromboembolic events was not different between patients who received concomitant erythropoietin therapy and those who did not, 4.8% and 8.6%, respectively (P = .54). A higher number of venous thrombotic episodes occurred in the highโdose corticosteroid group compared with the lowโdose corticosteroid therapy group (12% vs 6%), but the difference was not statistically significant (P = .3).
CONCLUSIONS.
The incidence of deep vein thrombosis is lower than previously reported in the literature. There was a trend to a higher incidence of thrombosis in patients receiving highโdose corticosteroid therapy. Cancer 2008. ยฉ 2008 American Cancer Society.
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