Abdallah Al-ola, Atrash Shebli, Shahid Zainab, Jameel Muzaffar, Grazziutti Monica, Apewokin Senu, Kumar Naveen S, Restrepo Alejandro, Waheed Sarah, Van Rhee Frits, Heuck Christoph J, Johann Donald, Barlogie Bart, Usmani Saad Z
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR.
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR.
Clin Lymphoma Myeloma Leuk. 2014 Jun;14(3):211-4. doi: 10.1016/j.clml.2013.11.004. Epub 2013 Nov 16.
Invasion of CNS in MM is an extremely rare occurrence that is associated with advanced disease with poor prognosis.
Our MM database identified 35 CNS MM cases presenting between January 1996 and March 2012. Descriptive analyses were performed on available data on patient characteristics, disease course, and outcomes.
The mean age at diagnosis was 55.4 years; 23.5% (n = 8) patients had elevated levels of beta-2-microglobulin > 5.5 mg/L; 68.6% (n = 24) of patients had elevated lactate dehydrogenase (LDH) levels (≥ 2 times upper limit of normal); and 14% (n = 5) of patients had secondary plasma cell leukemia. Magnetic resonance imaging (MRI), which was performed in 34 patients, showed diffuse or localized leptomeningeal disease in 20 patients (58.8%). Monoclonal malignant plasma cells were found by CSF analysis in all 35 patients. In total, 31 patients received chemotherapy, including intrathecal chemotherapy as a part of their treatment, with a median survival of 4 months after CNS MM diagnosis.
In our experience, CNS MM is an aggressive terminal disease feature associated with high beta-2-microglobulin level, high LDH level, and secondary plasma cell leukemia. This study highlights an unmet need in this subset of patients with high-risk, relapsed or refractory MM.
Achieving adequate CSF penetration while limiting the off-target effects needs to be considered in MM-specific novel drug development.
多发性骨髓瘤(MM)侵犯中枢神经系统(CNS)极为罕见,与晚期疾病及不良预后相关。
我们的MM数据库确定了1996年1月至2012年3月期间出现的35例CNS-MM病例。对患者特征、疾病进程和结局的可用数据进行了描述性分析。
诊断时的平均年龄为55.4岁;23.5%(n = 8)的患者β2-微球蛋白水平升高>5.5 mg/L;68.6%(n = 24)的患者乳酸脱氢酶(LDH)水平升高(≥正常上限的2倍);14%(n = 5)的患者患有继发性浆细胞白血病。34例患者进行了磁共振成像(MRI),其中20例(58.8%)显示弥漫性或局限性软脑膜疾病。所有35例患者的脑脊液分析均发现单克隆恶性浆细胞。共有31例患者接受了化疗,包括鞘内化疗作为其治疗的一部分,CNS-MM诊断后的中位生存期为4个月。
根据我们的经验,CNS-MM是一种侵袭性终末期疾病特征,与高β2-微球蛋白水平、高LDH水平及继发性浆细胞白血病相关。本研究突出了这一高危、复发或难治性MM患者亚组中未满足的需求。
在MM特异性新药研发中,需要考虑在实现足够的脑脊液渗透的同时限制脱靶效应。