Autologous Hematopoietic Stem Cell Transplantation for Paraneoplastic Cerebellar Degeneration.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
Victor Guerra, Jose Maria Cabrera-Maqueda, Raquel Ruiz-Garcia, Juan Francisco Luchoro, Elianet Fonseca, Mar Guasp, Yolanda Blanco, Maria Suarez-Lledo, Francesc Fernandez-Aviles, Carmen Martinez, Montserrat Rovira, Josep Dalmau, Francesc Graus, Albert Saiz, Eugenia Martinez-Hernandez
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Abstract

Background and objectives: The aim of this study was to describe 2 patients with paraneoplastic cerebellar degeneration (PCD) treated with autologous hematopoietic stem cell transplantation (AHSCT).

Methods: Off-label AHSCT was performed at Hospital Clinic Barcelona, including stem cell mobilization (cyclophosphamide, filgrastim), plasma exchange, and a nonmyeloablative regimen (cyclophosphamide, antithymocyte globulin, rituximab [RTX]).

Results: A 38-year-old woman developed anti-Yo-associated PCD 17 months after treatment of a gynecologic cancer (without evidence of tumor recurrence). Despite treatment with steroids and RTX, she became unable to walk. AHSCT resulted in progressive improvement, no longer needing assistance to walk 9 months after AHSCT. Tumor recurrence, without neurologic worsening, was identified 16 months after AHSCT, and chemotherapy was restarted. At the last follow-up (46 months), she continues on chemotherapy without neurologic deterioration. A 48-year-old man developed PCD associated with Tr/delta/notch-like epidermal growth factor-related receptor antibodies. Axillary lymph node biopsy demonstrated Hodgkin lymphoma. Chemoradiation resulted in complete tumor response, but cerebellar ataxia worsened despite treatment with steroids and IV immunoglobulins. Ten months after cerebellar symptom onset, he underwent AHSCT resulting in neurologic improvement. At the last follow-up, 39 months after AHSCT, he remains independent in activities of daily living.

Discussion: In our experience, AHSCT is worth to be considered in patients with progressive PCD refractory to conventional oncological and immunotherapy treatments.

Classification of evidence: This is a single observational study without controls and provides Class IV evidence.

自体造血干细胞移植治疗副肿瘤性小脑变性。
背景和目的:本研究的目的是描述2例用自体造血干细胞移植(AHSCT)治疗的副肿瘤小脑变性(PCD)。方法:在巴塞罗那医院诊所进行标签外AHSCT,包括干细胞动员(环磷酰胺、非格司提姆)、血浆交换和非清髓方案(环磷酰胺、抗胸腺细胞球蛋白、利妥昔单抗[RTX])。结果:一名38岁女性在接受妇科肿瘤治疗17个月后出现抗yo相关性PCD(无肿瘤复发迹象)。尽管接受了类固醇和RTX治疗,她还是无法行走。AHSCT导致了渐进式改善,在AHSCT后9个月不再需要辅助行走。在AHSCT后16个月发现肿瘤复发,无神经系统恶化,并重新开始化疗。最后一次随访(46个月),患者继续化疗,神经系统无恶化。1例48岁男性患PCD伴Tr/ δ /缺口样表皮生长因子相关受体抗体。腋窝淋巴结活检显示霍奇金淋巴瘤。放化疗导致肿瘤完全缓解,但小脑性共济失调恶化,尽管治疗类固醇和静脉免疫球蛋白。小脑症状出现10个月后,他接受了AHSCT治疗,神经系统得到改善。在AHSCT后39个月的最后一次随访中,他在日常生活活动中保持独立。讨论:根据我们的经验,对于难以接受常规肿瘤和免疫治疗的进行性PCD患者,AHSCT是值得考虑的。证据分类:这是一项没有对照的单一观察性研究,提供了IV级证据。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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