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Is tocilizumab a potential therapeutic option for refractory unicentric Castleman disease?

机译:拍摄是难治性无限卡斯克曼疾病的潜在治疗选择吗?

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摘要

Abstract Castleman disease is a rare lymphoproliferative disorder with 2 distinctly defined clinical forms. While multicentric Castleman disease (UCD) poses a potential therapeutic challenge, unicentric variant has historically been considered curable with surgical resection. Hence, little is known to guide management of patients with UCD, refractory to surgical resection and combination chemotherapy. We present a case of a patient, negative for HIV and HHV‐8, who had an unsuccessful surgical intervention and no response to radiotherapy and chemotherapy. He had severe paraneoplastic pemphigus and was treated with tocilizumab, an anti‐interleukin‐6 receptor monoclonal antibody that has demonstrated good response rates in multicentric Castleman disease but demonstrated no clinical response despite 2?months of treatment. Our report is the first to describe a lack of response to tocilizumab in the rare setting of refractory UCD and discuss potential for distinct disease biology.
机译:摘要Castleman病是一种罕见的淋巴升降症,具有2个明确定义的临床形式。 虽然多中心卡斯勒疾病(UCD)构成了潜在的治疗挑战,但无限的变种历史上被认为是用手术切除治愈的。 因此,众所周知,对UCD患者的管理指导,对手术切除和组合化疗的难以进行难治。 我们提出了患者的病例,对HIV和HHV-8负面,手术干预不成功,没有对放射治疗和化疗的反应。 他患有严重的寄生虫Pemphigus,并用Tocolizumab处理,一种抗白细胞介素-6受体单克隆抗体,表明了多中心卡斯克疾病中的良好反应率,但尽管2个月的治疗,但仍然证明无临床反应。 我们的报告是第一个描述在难治性UCD的罕见环境中缺乏对康普拉姆的回应,并探讨了不同疾病生物学的潜力。

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