Hutto Spencer K, Kyle Kevin, Cavanagh Julien J, Reda Haatem, Venna Nagagopal
Division of Hospital Neurology, Department of Neurology, Emory University School of Medicine, 12 Executive Park Dr NE, Atlanta, GA, 30329, USA.
Division of Neuroimmunology and Neuroinfectious Diseases, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
J Neurol. 2022 Apr;269(4):2064-2072. doi: 10.1007/s00415-021-10793-2. Epub 2021 Sep 6.
Tumor necrosis factor (TNF) alpha is critical in the development of granulomas and multiple recent reports have highlighted the role of infliximab, an infused TNF alpha inhibitor, in the treatment of neurosarcoidosis. As a self-injected TNF alpha inhibitor, adalimumab has certain advantages over infused medications, including greater patient freedom and autonomy. Experience with adalimumab is not well reported in the literature.
To report clinical experience with adalimumab in the treatment of central nervous system (CNS) sarcoidosis by combining observations in our center with those that have been reported in the literature.
Patients were identified from the Mass General Brigham Research Patient Data Registry and in the literature by searching PubMed. Patients with CNS manifestations of sarcoidosis treated with adalimumab were included for retrospective review and analyzed for baseline characteristics, treatment indications, outcomes, and adverse effects.
Adalimumab was commonly started after failure of or intolerance to infliximab and methotrexate. Of those with adequate follow-up, 5/10 ultimately improved, remission was maintained in 3/10, and 2/10 with active disease remained stable without further worsening. One patient suffered a relapse, likely multifactorial in etiology, but has remained relapse free on adalimumab for 10 months subsequently. Three patients ultimately discontinued adalimumab.
Preliminary evidence suggests that adalimumab may be a reasonable therapeutic option for patients with neurosarcoidosis affecting the CNS, including those with medically refractory disease.
肿瘤坏死因子(TNF)α在肉芽肿形成过程中起关键作用,近期多项报告强调了英夫利昔单抗(一种静脉输注的TNFα抑制剂)在神经结节病治疗中的作用。作为一种自我注射的TNFα抑制剂,阿达木单抗相较于静脉输注药物具有一定优势,包括患者有更大的自由度和自主性。关于阿达木单抗的使用经验在文献中报道较少。
通过结合我们中心的观察结果与文献报道,报告阿达木单抗治疗中枢神经系统(CNS)结节病的临床经验。
从麻省总医院布莱根妇女医院研究患者数据登记处以及通过检索PubMed确定患者。纳入接受阿达木单抗治疗的有CNS结节病表现的患者进行回顾性分析,分析其基线特征、治疗指征、结局和不良反应。
阿达木单抗通常在英夫利昔单抗和甲氨蝶呤治疗失败或不耐受后开始使用。在有充分随访的患者中,10例中有5例最终病情改善,10例中有3例维持缓解,2例仍有活动性疾病的患者病情保持稳定未进一步恶化。1例患者复发,病因可能是多因素的,但随后在阿达木单抗治疗下10个月未再复发。3例患者最终停用阿达木单抗。
初步证据表明,阿达木单抗对于患有影响CNS的神经结节病的患者,包括那些药物难治性疾病患者,可能是一种合理的治疗选择。