Lambert Nicolas, Forte Florence, El Moussaoui Majdouline, Monseur Justine, Raus Nicole, Polushin Alexey, Michonneau David, Shultz Carl, Hogan William J, Balaguer-Roselló Aitana, Gil-Perotín Sara, Brijs Jan, Chauvet Paul, Gavriilaki Maria, Carre Martin, Dulamea Adriana Octaviana, Chalandon Yves, Salmenniemi Urpu, Duminuco Andrea, Ram Ron, García-Cadenas Irene, Porto Gaetana, Nguyen Stéphanie, Smallbone Portia, González-Vicent Marta, Santoro Jonathan D, Willems Evelyne, Baron Frédéric, Servais Sophie, Beguin Yves, Maquet Pierre
Department of Neurology, University Hospital of Liège, 4000 Liège, Belgium.
Department of Infectious diseases and General Internal Medicine, University Hospital of Liège, 4000 Liège, Belgium.
Brain. 2025 Apr 3;148(4):1122-1133. doi: 10.1093/brain/awae340.
Despite the growing evidence supporting the existence of CNS involvement in acute and chronic graft-versus-host disease (CNS-GvHD), the characteristics and course of the disease are still largely unknown. In this multicentre retrospective study, we analysed the clinical, biological, radiological and histopathological characteristics, as well as the clinical course of 66 patients diagnosed with possible CNS-GvHD (pCNS-GvHD), selected by predetermined diagnostic criteria. Results were then contrasted depending on whether pCNS-GvHD onset occurred before or after Day 100 following allogeneic haematopoietic stem cell transplantation (allo-HSCT). The median time between allo-HSCT and pCNS-GvHD onset was 149 days (interquartile range25-75 48-321), and pCNS-GvHD onset occurred before Day 100 following transplantation in 44% of patients. The most frequent findings at presentation were cognitive impairment (41%), paresis (21%), altered consciousness (20%), sensory impairment (18%) and headache (15%). Clinical presentation did not significantly differ between patients with pCNS-GvHD occurring before or after Day 100 following transplantation. Brain MRI found abnormalities compatible with the clinical picture in 57% of patients, while CT detected abnormalities in only 7%. Seven patients had documented spinal cord MRI abnormalities, all of them with pCNS-GvHD occurring after Day 100 following transplantation. In the CSF, the white blood cell count was increased in 56% of the population (median 18 cells/μl). Histopathological analyses were performed on 12 specimens and were suggestive of pCNS-GvHD in 10. All compatible specimens showed parenchymal and perivascular infiltration by CD3+ and CD163+ cells. Immunosuppressive therapy was prescribed in 97% of patients, achieving complete clinical response in 27%, partial improvement in 47% and stable disease in 6%. Response to immunosuppressive therapy did not differ significantly between patients with pCNS-GvHD occurring before or after Day 100 following transplantation. Clinical relapse was observed in 31% of patients who initially responded to treatment. One-year overall survival following pCNS-GvHD onset was 41%. Onset before Day 100 following haematopoietic stem cell transplantation [hazard ratio with 95% confidence interval: 2.1 (1.0-4.5); P = 0.041] and altered consciousness at initial presentation [3.0 (1.3-6.7); P = 0.0077] were associated with a reduced 1-year overall survival probability. Among surviving patients, 61% had neurological sequelae. This study supports that immune-mediated CNS manifestations may occur following allo-HSCT. These can be associated with both acute and chronic GvHD and carry a grim prognosis. The clinical presentation as well as the radiological and biological findings appear variable.
尽管越来越多的证据支持中枢神经系统参与急性和慢性移植物抗宿主病(CNS-GvHD),但该疾病的特征和病程仍大多未知。在这项多中心回顾性研究中,我们分析了66例根据预定诊断标准确诊为可能的CNS-GvHD(pCNS-GvHD)患者的临床、生物学、放射学和组织病理学特征以及临床病程。然后根据pCNS-GvHD发病是在异基因造血干细胞移植(allo-HSCT)后第100天之前还是之后发生,对结果进行对比。allo-HSCT与pCNS-GvHD发病之间的中位时间为149天(四分位间距25-75:48-321),44%的患者pCNS-GvHD发病发生在移植后第100天之前。最常见的表现为认知障碍(41%)、轻瘫(21%)、意识改变(20%)、感觉障碍(18%)和头痛(15%)。移植后第100天之前或之后发生pCNS-GvHD的患者临床表现无显著差异。脑部MRI在57%的患者中发现与临床表现相符的异常,而CT仅在7%的患者中检测到异常。7例患者记录有脊髓MRI异常,所有这些患者的pCNS-GvHD均发生在移植后第100天之后。脑脊液中,56%的患者白细胞计数升高(中位值18个细胞/μl)。对12份标本进行了组织病理学分析,其中10份提示为pCNS-GvHD。所有相符的标本均显示实质和血管周围有CD3+和CD163+细胞浸润。97%的患者接受了免疫抑制治疗,27%的患者实现了完全临床缓解,47%的患者部分改善,6%的患者病情稳定。移植后第100天之前或之后发生pCNS-GvHD的患者对免疫抑制治疗的反应无显著差异。最初对治疗有反应的患者中有31%观察到临床复发。pCNS-GvHD发病后1年总生存率为41%。造血干细胞移植后第100天之前发病[风险比及95%置信区间:2.1(1.0-4.5);P = 0.041]以及初始表现为意识改变[3.0(1.3-6.7);P = 0.0077]与1年总生存概率降低相关。在存活患者中,61%有神经后遗症。这项研究支持allo-HSCT后可能出现免疫介导的中枢神经系统表现。这些表现可能与急性和慢性移植物抗宿主病均相关,且预后不佳。临床表现以及放射学和生物学发现似乎各不相同。