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我如何治疗原发性纵隔 B 细胞淋巴瘤。

How I treat primary mediastinal B-cell lymphoma.

机构信息

Division of Pediatric Hematology/Oncology, Department of Pediatrics, and Division of Hematology/Oncology, Department of Medicine, Weill Cornell Medical College, New York, NY.

出版信息

Blood. 2018 Aug 23;132(8):782-790. doi: 10.1182/blood-2018-04-791566. Epub 2018 Jul 5.

Abstract

The World Health Organization now recognizes primary mediastinal B-cell lymphoma (PMBCL) as a unique clinical and biologic entity. PMBCL is distinct from other B-cell non-Hodgkin lymphoma subtypes and has features that overlap with classical Hodgkin lymphoma, including a peak incidence in the adolescent and young adult population, mediastinal presentation of disease, and molecular alterations in JAK2 and programmed death ligands. Because PMBCL is rare, there are few prospective clinical trials to guide therapy, resulting in no single standard of care. Given the long life expectancy of survivors of PMBCL, treatment approaches must balance maximizing cure while minimizing long-term toxicity. In this article, I review my approach to the treatment of PMBCL, incorporating data from adult and pediatric studies, as well as recent advances in our understanding of the molecular basis of PMBCL.

摘要

世界卫生组织现在将原发性纵隔 B 细胞淋巴瘤 (PMBCL) 确认为一种独特的临床和生物学实体。PMBCL 与其他 B 细胞非霍奇金淋巴瘤亚型不同,具有与经典霍奇金淋巴瘤重叠的特征,包括在青少年和年轻成人中的高发、疾病的纵隔表现以及 JAK2 和程序性死亡配体的分子改变。由于 PMBCL 罕见,几乎没有前瞻性临床试验来指导治疗,因此没有单一的治疗标准。鉴于 PMBCL 幸存者的预期寿命长,治疗方法必须在最大限度地提高治愈率的同时,最大限度地降低长期毒性。在本文中,我将回顾我治疗 PMBCL 的方法,纳入了来自成人和儿科研究的数据,以及我们对 PMBCL 分子基础的最新认识。

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