达拉单抗、波马度胺、长春新碱、丙卡嗪、地塞米松联合治疗瘦脑膜骨髓瘤病例1例

IF 0.7 Q4 HEMATOLOGY Case Reports in Hematology Pub Date : 2022-08-31 eCollection Date: 2022-01-01 DOI:10.1155/2022/4081971
Jew Win Kuan, Sing Ling Chai, Pathmanathan Rajadurai, Lee Gong Lau, Joseph Uchang, Sharifah Noor Akmal Syed Husain
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引用次数: 2

摘要

多发性骨髓瘤(MM) (MM-CNS)以轻脑膜骨髓瘤病或脑实质浆细胞瘤的形式累及中枢神经系统(CNS)是罕见的,给临床诊断和治疗带来了挑战。我们想报告一例脑脊膜骨髓瘤病,并说明挑战。1例61岁男性,诊断为MM伴左侧椎旁浆细胞瘤,R-ISS II型,高度怀疑双发性MM, TP53或del(17p)双等位基因异常和IGH异常(视定义而定),接受来那度胺- bor替佐米-地塞米松治疗和局部放疗,后来全身性复发并进展为MM- cns,表现为轻脑膜骨髓瘤病。一种以前未报道的改良的以中枢神经系统为基础的治疗,包括达拉单抗、泊马度胺、长春新碱、丙卡嗪和地塞米松,带来了快速的临床改善,值得进一步研究。鞘内应用硫替帕可能会提高疗效。
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A Case Report of Leptomeningeal Myelomatosis and Rapid Improvement with Regimen Consisting of Daratumumab, Pomalidomide, Vincristine, Procarbazine, and Dexamethasone.

Central nervous system (CNS) involvement in multiple myeloma (MM) (MM-CNS) in the form of leptomeningeal myelomatosis or brain parenchyma plasmacytoma is rare, causing challenges in clinical diagnosis and treatment. We would like to report a case of leptomeningeal myelomatosis and illustrated the challeges. A 61-year-old man was diagnosed with MM with left paravertebral plasmacytoma, R-ISS II with high suspicion of double-hit MM, either biallelic aberrancy of TP53 or del(17p) and IGH aberrancy depending on the definition chosen, treated with lenalidomide-bortezomib-dexamethasone and local radiotherapy, later developed systemic relapse and progression to MM-CNS in the form of leptomeningeal myelomatosis. A modified CNS-based treatment not reported before, consisting of daratumumab, pomalidomide, vincristine, procarbazine, and dexamethasone, brought a rapid clinical improvement and warrants a further study. Incorporation of intrathecal thiotepa into the regimen would likely increase the efficacy.

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审稿时长
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