自体干细胞移植11年后多发性骨髓瘤孤立性中枢神经系统(CNS)复发:病例报告。

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL AME Case Reports Pub Date : 2024-09-12 eCollection Date: 2024-01-01 DOI:10.21037/acr-24-19
Eduardo Edmundo Reynoso-Gómez, Carlos Eduardo Quintero-Hernández
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引用次数: 0

摘要

背景:多发性骨髓瘤(MM)在中枢神经系统(CNS)复发会带来不良预后,通常发生在干细胞移植后的短时间内,总体生存期较短。孤立的中枢神经系统复发非常罕见,目前尚无标准治疗方法:病例描述:我们接诊了一名中枢神经系统MM孤立性复发的59岁男性患者,他在11年前接受了自体干细胞移植(ASCT)和沙利度胺维持治疗。他因马尾综合征回到我们的诊所,核磁共振(NMR)发现了脊柱病变,并进行了腰椎穿刺,在他的脑脊液(CSF)中发现了浆细胞。起初,他接受了甲氨蝶呤和类固醇+放疗的鞘内化疗,在每两周服用几次药物后,浆细胞消失了。后来,他又接受了泊马度胺/地塞米松治疗,共12个周期,临床反应良好,运动功能恢复了80%:在这例罕见的中枢神经系统肿瘤晚期复发病例中,我们证明了IT化疗辅以基于泊马度胺的全身治疗是安全有效的。在双特异性、嵌合抗原受体-T(CAR-T)细胞甚至达拉单抗或司来诺等新疗法尚未广泛应用的情况下,这一点尤为重要。在这种特殊情况下,还需要进一步的临床经验来证实这一观察结果,并为这一罕见的患者群体确定最佳的总体策略。
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Isolated central nervous system (CNS) relapse of multiple myeloma 11 years after autologous stem cell transplantation: a case report.

Background: Multiple myeloma (MM) relapse in the central nervous system (CNS) confers an adverse prognosis, usually occurring in a short period after stem cell transplant and with a short overall survival. Isolated CNS relapse is so rare that there is no current standard treatment.

Case description: We present a 59-year-old male with an isolated CNS MM relapse, who had received autologous stem-cell transplant (ASCT) and thalidomide maintenance 11 years prior. He returned to our clinic with cauda equina syndrome and a nuclear magnetic resonance (NMR) identified a spinal lesion, a lumbar puncture was performed and plasma cells were identified in his cerebrospinal fluid (CSF). He was initially treated with intrathecal (IT) chemotherapy with methotrexate and steroid + radiotherapy and plasma cells disappeared after a few bi-weekly doses. Later on, treatment with pomalidomide/dexamethasone was given for 12 cycles with good clinical response with 80% recovery of his motor function.

Conclusions: In this rare case of a very late CNS MM relapse, we demonstrate that IT chemotherapy complemented with a systemic pomalidomide-based treatment is safe and effective. This is particularly important in contexts where newer therapies such as bispecifics, chimeric antigen receptor-T (CAR-T) cells or even daratumumab or selinexor are not widely available. Further clinical experience in this particular scenario will be required to confirm this observation and define overall the best strategy for this rare group of patients.

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