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Randomized Controlled Trial
. 2020 May 1;59(9):1149-1153.
doi: 10.2169/internalmedicine.3800-19. Epub 2020 Feb 1.

Lenalidomide Treatment for Thalidomide-refractory POEMS Syndrome: A Prospective Single-arm Clinical Trial

Affiliations
Randomized Controlled Trial

Lenalidomide Treatment for Thalidomide-refractory POEMS Syndrome: A Prospective Single-arm Clinical Trial

Tomoki Suichi et al. Intern Med. .

Abstract

Objective A randomized controlled trial has shown the efficacy of thalidomide against polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome; however, there are still refractory patients. We studied the effects of lenalidomide, a derivative of thalidomide, on patients refractory to thalidomide. Methods This prospective single-arm trial evaluated the safety and efficacy of lenalidomide plus dexamethasone in refractory or recurrent patients with POEMS syndrome. The regimen was administered as six 28-day cycles with lenalidomide on days 1-21 (15 mg in cycle 1, and 25 mg in cycle 2-6) plus dexamethasone once a week (20 mg). The primary endpoints were the rate of reduction in the serum vascular endothelial growth factor (VEGF) level at 24 weeks and the incidence of adverse events. This trial was registered with ClinicalTrial.gov, NCT02193698. Results Between July 2014 and December 2015, five men were enrolled. All patients had been refractory to thalidomide plus dexamethasone for more than 24 weeks. The mean rate of reduction in the serum VEGF level at 24 weeks was 59.6%±8.3% (p=0.0003). The mean serum VEGF level decreased from 2,466±771 pg/mL to 974±340 pg/mL. No serious adverse events were observed, and all patients completed six cycles treatment. Discussion Lenalidomide is a therapeutic option for thalidomide-refractory patients with POEMS syndrome.

Keywords: POEMS syndrome; VEGF; clinical trial; lenalidomide; thalidomide.

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Conflict of interest statement

The authors state that they have no Conflict of Interest (COI).

Figures

Figure.
Figure.
Sequential changes in the serum VEGF level. (A) Sequential changes in the rate of reduction in the serum VEGF level. The primary endpoint was the mean rate of reduction in the serum VEGF level at 24 weeks (59.6%±8.3%; 90% CI 50.8-68.4; p=0.0003). (B) Sequential changes in the serum VEGF level. CI: confidence interval, SD: standard deviation, VEGF: vascular endothelial growth factor

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