Dittus Christopher, Grover Natalie, Ellsworth Steven, Tan Xianming, Park Steven I
a Division of Hematology and Oncology Medicine , University of North Carolina at Chapel Hill , Chapel Hill , NC , USA.
b Division of Hematology and Oncology Medicine , University of North Carolina at Chapel Hill , Chapel Hill , NC , USA.
Leuk Lymphoma. 2018 Sep;59(9):2121-2127. doi: 10.1080/10428194.2017.1416365. Epub 2018 Jan 5.
Plasmablastic lymphoma (PBL) is a rare and aggressive form of B-cell non-Hodgkin lymphoma. This subtype of lymphoma has a post-germinal center cell-of-origin called the plasmablast, and the immunophenotype is more consistent with that of a plasma cell than a lymphocyte. Because of these unique features, PBL is notoriously difficult to treat. Case reports and small reviews have evaluated the addition of agents directed against plasma cell disorders in combination with traditional lymphoma-directed regimens. We describe the largest case series to date, with the longest follow-up, evaluating bortezomib in combination with etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin (V-EPOCH) for the treatment of PBL. Our results show that this is a safe and effective regimen with an overall and complete response rate of 100% and 2-year overall survival of 50%.
浆母细胞淋巴瘤(PBL)是一种罕见且侵袭性的B细胞非霍奇金淋巴瘤。这种淋巴瘤亚型具有一种生发中心后起源的细胞,称为浆母细胞,其免疫表型与浆细胞而非淋巴细胞更为一致。由于这些独特特征,PBL治疗难度极大。病例报告和小型综述评估了针对浆细胞疾病的药物与传统淋巴瘤治疗方案联合使用的情况。我们描述了迄今为止最大的病例系列,随访时间最长,评估了硼替佐米联合依托泊苷、泼尼松、长春新碱、环磷酰胺和多柔比星(V-EPOCH)治疗PBL的情况。我们的结果表明,这是一种安全有效的方案,总缓解率和完全缓解率均为100%,2年总生存率为50%。