Department of Medicine, Division of Hematology, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, USA.
Department of Molecular and Cellular Pharmacology, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, USA.
Expert Rev Hematol. 2023 May;16(5):333-348. doi: 10.1080/17474086.2023.2206557. Epub 2023 Apr 28.
Extranodal marginal zone lymphoma (EMZL) of mucosa-associated lymphoid tissue is an indolent lymphoma originating from marginal zone B-cells and associated with chronic inflammation. EMZL demonstrates distinct genomic alterations according to the primary extranodal site of disease but commonly affects signaling pathways including NF-ĸB, B-cell receptor, and NOTCH. Treatment with radiation therapy is commonly implemented in localized diseases, and multiple agents are available for patients with advanced-stage diseases in need of therapy. Bendamustine with rituximab is a frontline platform associated with high efficacy.
Clinical features, diagnosis, genomics, models enabling risk stratification, treatment options, and future directions.
The lack of consistent genotyping profile in EMZL precludes the development of tissue and circulatory biomarkers for the diagnosis, risk stratification, and monitoring of minimal residual disease. Furthermore, the biological heterogeneity observed in extranodal sites associated with overall limited genomic data prevents the testing of druggable pathways aiming for a personalized treatment approach. Future clinical trials should focus on EMZL considering the unique clinical characteristics in the eligibility criteria and response assessment to better inform efficacy of novel agents and delineate sequences of therapies.
黏膜相关淋巴组织结外边缘区淋巴瘤(EMZL)是一种惰性淋巴瘤,起源于边缘区 B 细胞,并与慢性炎症相关。根据疾病的主要结外部位,EMZL 表现出明显的基因组改变,但通常会影响信号通路,包括 NF-κB、B 细胞受体和 NOTCH。对于局限性疾病,通常采用放射治疗,对于需要治疗的晚期疾病患者,有多种药物可供选择。含苯达莫司汀和利妥昔单抗的方案是一种疗效较高的一线治疗平台。
临床特征、诊断、基因组学、风险分层模型、治疗选择和未来方向。
EMZL 缺乏一致的基因分型特征,这使得用于诊断、风险分层和监测微小残留病的组织和循环生物标志物的开发受到限制。此外,与总体上有限的基因组数据相关的结外部位的生物学异质性,阻止了对可用药的通路进行测试,以实现个性化的治疗方法。未来的临床试验应考虑到 EMZL 的独特临床特征,在纳入标准和反应评估中,以更好地告知新型药物的疗效,并确定治疗方案的顺序。