Vernino Steven, O'Neill Brian Patrick, Marks Randolph S, O'Fallon Judith R, Kimmel David W
Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
Neuro Oncol. 2004 Jan;6(1):55-62. doi: 10.1215/S1152851703000395.
Paraneoplastic neurological disorders are devastating remote effects of malignancy. Despite compelling evidence of an autoimmune pathogenesis, empiric immunomodulatory treatment of these disorders is often ineffective. However, very few systematic studies have been conducted, and the treatment of patients without active malignancy has not been addressed. We conducted a prospective open-label treatment study of plasma exchange plus conventional cancer chemotherapy (10 patients) or plasma exchange plus continuous oral cyclophosphamide (10 patients). All patients had progressive symptoms and at least moderate disability at enrollment (mean Rankin score, 3.4). Patients who had experienced symptoms for more than 12 months were excluded (mean duration of symptoms at enrollment, 3.6 months). The primary outcome measure was change in quantitative disability measures (Rankin and Barthel scores) after 6 months of treatment; a positive response was defined as stability or improvement in disability. Overall, 50% of patients had a positive response at 6 months (6 patients had improved by at least 1 Rankin grade). Patients with good outcome tended to be those with less disability at time of enrollment. Hematologic toxicity was common among those receiving cyclophosphamide. Aggressive immunosuppression early in the clinical course should be considered in patients who have paraneoplastic neurological disorders, even when there is no evidence of active malignancy.
副肿瘤性神经系统疾病是恶性肿瘤造成的严重远隔效应。尽管有确凿证据表明其发病机制为自身免疫性,但对这些疾病进行的经验性免疫调节治疗往往无效。然而,很少有系统性研究,且未涉及对无活动性恶性肿瘤患者的治疗。我们开展了一项前瞻性开放标签治疗研究,对10例患者采用血浆置换加传统癌症化疗,对另外10例患者采用血浆置换加持续口服环磷酰胺。所有患者在入组时均有进行性症状且至少有中度残疾(平均Rankin评分3.4)。症状出现超过12个月的患者被排除(入组时症状的平均持续时间为3.6个月)。主要结局指标为治疗6个月后定量残疾指标(Rankin和Barthel评分)的变化;阳性反应定义为残疾稳定或改善。总体而言,50%的患者在6个月时有阳性反应(6例患者至少改善了1个Rankin等级)。预后良好的患者往往是入组时残疾程度较轻的患者。血液学毒性在接受环磷酰胺治疗的患者中很常见。对于副肿瘤性神经系统疾病患者,即使没有活动性恶性肿瘤的证据,在临床病程早期也应考虑积极免疫抑制治疗。