4.2 Review

Thalidomide and Lenalidomide for Refractory Systemic/Cutaneous Lupus Erythematosus Treatment A Narrative Review of Literature for Clinical Practice

期刊

JCR-JOURNAL OF CLINICAL RHEUMATOLOGY
卷 27, 期 6, 页码 248-259

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/RHU.0000000000001160

关键词

cutaneous lupus erythematosus; lenalidomide; peripheral neuropathy; systemic lupus erythematosus; thalidomide

资金

  1. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [2015/03756-4]
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [305068/2014-8, 303422/2015-7]
  3. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [15/03756-4] Funding Source: FAPESP

向作者/读者索取更多资源

Thalidomide has shown excellent efficacy in the treatment of refractory cutaneous lupus, but poses a high risk of neurotoxicity. Lenalidomide is a promising drug for skin lupus treatment, particularly due to its lower frequency of nerve side effects.
Background: Thalidomide has shown exceptional results in systemic/cutaneous lupus erythematosus(SLE/CLE). Recently, lenalidomide has been also prescribed for SLE/CLE treatment. Literature regarding efficacy/adverse events for these drugs is scarce with a single systematic review and meta-analysis focused solely on thalidomide for refractory cutaneous lupus subtypes. Objective: We, therefore, addressed in this narrative review the efficacy/adverse effects of thalidomide and lenalidomide for SLE and CLE. In addition, we provide a specialist approach for clinical practice based on the available evidence. Results: Efficacy of thalidomide for refractory cutaneous lupus treatment was demonstrated by several studies, mostly retrospective with small sample size(<= 20). The frequency of peripheral polyneuropathy is controversial varying from 15-80% with no consistent data regarding cumulative dose and length of use. Drug withdrawn results in clinical partial/complete reversibility for most cases (70%). For lenalidomide, seven studies (small sample sizes) reported its efficacy for SLE/CLE with complete/partial response in all patients with a mean time to response of 3 months. Flare rate varied from 25-75% occurring 0.5-10 months after drug withdrawn. There were no reports of polyneuropathy/worsening of previous thalidomide-induced neuropathy, but most of them did not perform nerve conduction studies. Teratogenicity risk exist for both drugs and strict precautions are required. Conclusions: Thalidomide is very efficacious as an induction therapy for patients with severe/refractory cutaneous lupus with high risk of scarring, but its longstanding use should be avoided due to neurotoxicity. Lenalidomide is a promising drug for skin lupus treatment, particularly regarding the apparent lower frequency of nerve side effects.

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