Sierra Morales Fabian, Wright Robert B, Novo Jorge E, Arvanitis Leonidas D, Stefoski Dusan, Koralnik Igor J
Section of Neuroinfectious diseases Rush University Medical Center Chicago Illinois.
Department of Neurological Sciences Rush University Medical Center Chicago Illinois.
Ann Clin Transl Neurol. 2017 Jun 6;4(7):512-516. doi: 10.1002/acn3.428. eCollection 2017 Jul.
We present two natalizumab-treated multiple sclerosis patients who developed glioblastoma multiforme (GBM) with variable outcomes. One patient had an isocitrate dehydrogenase (IDH)-wildtype GBM with aggressive behavior, who declined treatment and died 13 weeks after symptoms onset. The other patient underwent resection of an IDH-mutant secondary GBM that arose from a previously diagnosed grade II astrocytoma. He is still alive 5 years after the diagnosis of GBM. JC virus was not detected in either case. Whether natalizumab played a role in the development of GBM in those patients deserves further investigation.
我们报告了两名接受那他珠单抗治疗的多发性硬化症患者,他们均发生了多形性胶质母细胞瘤(GBM),结局各异。一名患者患有异柠檬酸脱氢酶(IDH)野生型GBM,具有侵袭性,拒绝治疗,症状出现后13周死亡。另一名患者接受了IDH突变型继发性GBM的切除术,该GBM由先前诊断的II级星形细胞瘤发展而来。在GBM诊断后5年,他仍然存活。两例均未检测到JC病毒。那他珠单抗在这些患者GBM的发生中是否起作用值得进一步研究。