Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina, USA.
Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA.
Am J Hematol. 2023 Feb;98(2):300-308. doi: 10.1002/ajh.26784. Epub 2023 Jan 1.
Plasmablastic lymphoma (PBL) is a rare entity, commonly associated with immunosuppressed states such as human immunodeficiency virus (HIV) infection or solid organ transplant. The clinical course is characterized by high relapse rates and a poor prognosis, leading some clinicians to recommend aggressive frontline therapy. However, a specific review of limited stage (LS) PBL patients is not available to evaluate outcomes and justify treatment recommendations. We performed a retrospective review of LS PBL cases to provide insight into this rare disease. Our cohort consisted of 80 stage I or II PBL patients from 13 US academic centers. With a median follow up of 34 months (1-196), the 3-year progression-free survival (PFS) and overall survival (OS) of the entire cohort were 72% (95% CI 62, 83) and 79% (95% CI 70, 89), respectively. The 3-year PFS and OS of patients treated with frontline chemotherapy alone was 65% (95% CI 50, 84) and 71% (95% CI 56, 89), respectively, compared to 85% (95% CI 72, 100) and 96% (95% CI 89, 100), respectively, in patients treated with combined frontline chemotherapy with radiation consolidation. Our data demonstrate favorable outcomes in LS PBL with no improvements in outcome from aggressive frontline treatment including Hyper-CVAD or auto-SCT consolidation. Multivariate regression analysis (MRA) demonstrated improved PFS for patients receiving EPOCH based frontline therapy versus CHOP (HR: 0.23; p = 0.029). Frontline chemotherapy followed by radiation consolidation versus chemotherapy alone appeared to be associated with improved relapse and survival outcomes but did not show statistical significance in MRA.
浆母细胞淋巴瘤(PBL)是一种罕见的疾病,通常与免疫抑制状态相关,如人类免疫缺陷病毒(HIV)感染或实体器官移植。其临床病程以高复发率和预后不良为特征,这导致一些临床医生建议采用积极的一线治疗。然而,目前尚无针对局限性(LS)PBL 患者的专门回顾性研究来评估其结局并为治疗建议提供依据。我们对 LS PBL 病例进行了回顾性研究,以深入了解这种罕见疾病。我们的队列包括来自 13 个美国学术中心的 80 例 I 期或 II 期 PBL 患者。中位随访 34 个月(1-196),整个队列的 3 年无进展生存率(PFS)和总生存率(OS)分别为 72%(95%CI 62,83)和 79%(95%CI 70,89)。单独接受一线化疗的患者 3 年 PFS 和 OS 分别为 65%(95%CI 50,84)和 71%(95%CI 56,89),而接受一线化疗联合巩固性放疗的患者分别为 85%(95%CI 72,100)和 96%(95%CI 89,100)。我们的数据表明 LS PBL 患者的结局良好,而包括 Hyper-CVAD 或自体干细胞移植巩固在内的积极一线治疗并未改善患者结局。多变量回归分析(MRA)表明,接受 EPOCH 一线治疗的患者 PFS 优于接受 CHOP 治疗的患者(HR:0.23;p=0.029)。与单纯化疗相比,一线化疗后行放疗巩固治疗似乎与改善复发和生存结局相关,但在 MRA 中未显示出统计学意义。