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对难治性非转化型 CD30 蕈样肉芽肿采用 Brentuximab vedotin 治疗后出现戏剧性反应,从而能够进行异基因干细胞移植和长期完全缓解。

Dramatic response to brentuximab vedotin in refractory nontransformed CD30 mycosis fungoides allowing allogeneic stem cell transplant and long-term complete remission.

机构信息

Department of Dermatology, AP-HP Hôpital Saint-Louis, Paris, France.

Department of Pathology, AP-HP Hôpital Saint-Louis, Paris, France.

出版信息

Br J Dermatol. 2019 Jun;180(6):1517-1520. doi: 10.1111/bjd.17254. Epub 2019 Jan 1.

Abstract

The erythrodermic ulcerated form of mycosis fungoides (MF) is exceptional, and treatment of refractory cases is challenging. Brentuximab vedotin (BV) is a monoclonal antibody combined with monomethyl auristatin E, recently approved for the treatment of refractory CD30 cutaneous T-cell lymphoma. We report a case of refractory MF in a 56-year-old man with a long history of large-plaque parapsoriasis, as revealed by psoriasiform erythroderma, treated initially with cyclophosphamide, doxorubicin, vincristine and prednisone (CHOP) polychemotherapy, inducing a 2-year complete response. After relapse, interferon and gemcitabine were unsuccessful. Finally, treatment with BV was decided upon, despite the absence of CD30 expression. After three infusions of BV 1·8 mg kg , we achieved a complete and stable response, allowing an allogeneic stem cell transplant. The patient is still in complete remission, 19 months after the graft. This case illustrates the possibility of using BV in refractory CD30 MF as a salvage therapy.

摘要

蕈样肉芽肿(MF)的红皮病性溃疡性形式较为罕见,难治性病例的治疗颇具挑战。 Brentuximab vedotin(BV)是一种与单甲基奥瑞他汀 E 结合的单克隆抗体,最近被批准用于治疗难治性 CD30 皮肤 T 细胞淋巴瘤。我们报告了一例难治性 MF 病例,患者为 56 岁男性,有大斑块副银屑病的长期病史,表现为银屑病样红皮病,最初采用环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP)联合化疗,诱导 2 年完全缓解。缓解后复发,干扰素和吉西他滨治疗无效。最后,决定采用 BV 治疗,尽管没有 CD30 表达。在接受 BV 1.8 mg/kg 三次输注后,我们获得了完全且稳定的缓解,从而进行了异基因干细胞移植。在移植物后 19 个月,患者仍处于完全缓解状态。该病例说明,BV 可作为难治性 CD30 MF 的挽救治疗。

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