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药物性亚急性皮肤型狼疮红斑与 nab-紫杉醇治疗相关。

Drug-induced subacute cutaneous lupus erythematosus associated with nab-paclitaxel therapy.

机构信息

Department of Medicine, Dalhousie University, Halifax, NS.

出版信息

Curr Oncol. 2013 Oct;20(5):e484-7. doi: 10.3747/co.20.1546.

Abstract

Drug-induced lupus erythematosus (dile) syndromes are documented complications of chemotherapeutic agents, including paclitaxel. Subacute cutaneous lupus erythematosus (scle) is a distinct dile syndrome presenting with characteristic annular or papulosquamous skin lesions in a photosensitive distribution with associated high anti-ssa titres. Previously, dile syndromes complicating paclitaxel therapy have been attributed to polyethoxylated castor oil (Kolliphor EL: BASF, Ludwigshafen, Germany), the biologic solvent included in the drug's original formulation (Taxol: Bristol-Myers Squibb, Montreal, QC), rather than the parent chemotherapy molecule. Here, we report a characteristic case of drug-induced scle complicating treatment with nanoparticle albumin bound (nab)-paclitaxel (Abraxane: Celgene, Summit, NJ, U.S.A.), a solvent-free taxane formulation. The pertinent English-language literature is also discussed. This case report is the first to link solvent-free paclitaxel with scle, and it suggests that the parent molecule is responsible for the reaction.

摘要

药物诱导的红斑狼疮(DILE)综合征是化学治疗剂的已知并发症,包括紫杉醇。亚急性皮肤型红斑狼疮(SCLE)是一种独特的 DILE 综合征,表现为特征性的环形或丘疹鳞屑性皮肤损伤,分布于光敏部位,伴有高抗 SSA 滴度。以前,紫杉醇治疗引起的 DILE 综合征归因于聚氧乙烯蓖麻油(Kolliphor EL:BASF,Ludwigshafen,德国),这是药物原始配方中包含的生物溶剂(紫杉醇:百时美施贵宝,蒙特利尔,QC),而不是母体化疗药物分子。在这里,我们报告了一个使用纳米白蛋白结合紫杉醇(Abraxane:Celgene,Summit,NJ,美国)治疗引起的典型药物诱导的 SCLE 病例,这是一种无溶剂的紫杉醇制剂。还讨论了相关的英语文献。本病例报告是首例将无溶剂紫杉醇与 SCLE 联系起来的报告,这表明母体分子是导致这种反应的原因。

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