Hirunpattarasilp Chanawee, Fu Pingfu, Margevicius Seunghee Park, Mirsky Matthew, Bruno Debora, Mangla Ankit, Hoehn Richard Stephen, Rothermel Luke Daniel, Sheng Iris Yeong-Fung
Princess Srisavangavadhana Faculty of Medicine, Chulabhorn Royal Academy, Bangkok, Thailand.
Department of Neurology, University Hospitals Cleveland Medical Center, Cleveland, Ohio, United States.
Neurooncol Adv. 2025 Mar 4;7(1):vdaf048. doi: 10.1093/noajnl/vdaf048. eCollection 2025 Jan-Dec.
Multiple sclerosis (MS) patients are excluded from studies of immune checkpoint inhibitors (ICIs) due to concern for MS flare. This study aims to report the incidence of MS relapse, immune-related adverse events (irAEs), and cancer outcomes in MS patients with solid-organ malignancy treated with ICIs.
In this retrospective study, MS patients who received ICIs at University Hospitals Seidman Cancer Center were identified electronically. Information on MS relapses, irAEs, and cancer outcomes after ICI initiation was collected and analyzed.
Twelve patients were included in the study, all of whom had inactive MS. No patient experienced MS relapse or new lesions on brain MRI after ICI initiation. Two patients (16.7%) had severe irAEs (grade ≥ 3), which was acute pneumonitis. No deaths were associated. The objective response rate was 50%. An additional year of age was associated with a 14.2% decrease in the risk of developing severe irAEs (hazard ratio (HR) = 0.858; 95% confidence interval (CI): 0.798-0.922; < .0001) and a 10.3% decrease in the risk of disease progression (HR = 0.897; 95% CI: 0.823-0.976; = .0120). No significant difference in risk of having severe irAEs, overall survival, or progression-free survival was found between MS patients with and without DMTs.
Our study suggests that ICIs could be safely used in patients with inactive MS with a low risk of MS relapse and comparable irAE risk with the general population. Although larger studies are needed for confirmation, the benefit of using ICIs to treat solid-organ malignancies might outweigh the risk of withholding treatment for this population.
由于担心多发性硬化症(MS)病情发作,MS患者被排除在免疫检查点抑制剂(ICI)研究之外。本研究旨在报告接受ICI治疗的实体器官恶性肿瘤MS患者中MS复发、免疫相关不良事件(irAE)和癌症转归的发生率。
在这项回顾性研究中,通过电子方式确定了在大学医院西德曼癌症中心接受ICI治疗的MS患者。收集并分析了ICI开始治疗后MS复发、irAE和癌症转归的信息。
12例患者纳入研究,均为非活动性MS。ICI开始治疗后,无患者发生MS复发或脑MRI出现新病灶。2例患者(16.7%)发生严重irAE(≥3级),为急性肺炎。无死亡病例。客观缓解率为50%。年龄每增加1岁,发生严重irAE的风险降低14.2%(风险比[HR]=0.858;95%置信区间[CI]:0.798-0.922;P<0.0001),疾病进展风险降低10.3%(HR=0.897;95%CI:0.823-0.976;P=0.0120)。在接受和未接受疾病修饰治疗(DMT)的MS患者中,严重irAE风险、总生存期或无进展生存期无显著差异。
我们的研究表明,ICI可安全用于MS复发风险低且irAE风险与普通人群相当的非活动性MS患者。尽管需要更大规模的研究来证实,但使用ICI治疗实体器官恶性肿瘤对该人群的益处可能超过 withholding治疗的风险。 (注:“withholding treatment”直译为“ withholding治疗”,此处可能需要结合上下文进一步明确其准确含义,推测可能是指不进行某些治疗或延迟治疗等情况 )