University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Harrington Heart and Vascular Institute, University Hospitals, Cleveland, OH, United States of America; School of Medicine, Case Western Reserve University, Cleveland, OH, United States of America.
Int J Cardiol. 2021 Sep 15;339:146-149. doi: 10.1016/j.ijcard.2021.07.043. Epub 2021 Jul 26.
Background Cardiac diffuse large B-cell lymphoma (cDLBCL) is an extremely rare disease. Introduction of rituximab has significantly improved survival in non-cardiac DLBCL, but there is limited data regarding the effects on outcomes in cDLBCL. We sought to evaluate the outcomes of cDLBCL in both pre- and rituximab eras. Methods We identified all cDLBCL cases in the Surveillance, Epidemiology and End Results (SEER) registry from 1975 to 2016. We compared survival (overall and lymphoma-specific) of patients diagnosed prior to versus after rituximab approval in 2006. Results A total of 106 patients were included in the final analysis. Median age was 69.5 years, 67% of the patients were white and 64% had local stage I/II disease. 67% of the patients were diagnosed after 2006 and thus belonged to the rituximab era group. Overall, 77% received chemotherapy, 24% had surgery and 15% had radiotherapy. Median overall survival (OS) for the entire cohort was 22 months. Median OS was 16 months (95% CI, 0.55-31) for the pre-rituximab group, versus 26 months (95% CI, 7.5-45) for the rituximab group (p = 0.34). Median lymphoma-specific survival (LSS) was 30 months (95% CI, 8.0-52) for the pre-rituximab group versus 36 months (95% CI, 16-158) for the rituximab group (p = 0.30). OS and LSS were also not significantly different between the two era groups when stratified by chemotherapy. In multivariable analysis, both OS and LSS were associated with lymphoma stage, insurance status and age but not with diagnosis era or chemotherapy. Conclusions Cardiac DLBCLs are rare and affecting mostly the elderly. Younger age, limited disease stage, and having health insurance but not lymphoma diagnosis era were associated with better outcomes.
心脏弥漫性大 B 细胞淋巴瘤(cDLBCL)是一种极其罕见的疾病。利妥昔单抗的引入显著改善了非心脏 DLBCL 的生存,但关于其对 cDLBCL 结局的影响的数据有限。我们旨在评估 cDLBCL 在利妥昔单抗引入前后的结局。
我们从 1975 年至 2016 年在监测、流行病学和最终结果(SEER)登记处确定了所有 cDLBCL 病例。我们比较了在 2006 年利妥昔单抗批准前后诊断的患者的生存(总体和淋巴瘤特异性)。
共有 106 例患者纳入最终分析。中位年龄为 69.5 岁,67%的患者为白人,64%为局限性 I/II 期疾病。67%的患者在 2006 年后被诊断为 cDLBCL,因此属于利妥昔单抗治疗时代组。总体而言,77%的患者接受了化疗,24%的患者接受了手术,15%的患者接受了放疗。整个队列的中位总生存期(OS)为 22 个月。在利妥昔单抗治疗前组的中位 OS 为 16 个月(95%CI,0.55-31),利妥昔单抗治疗组的中位 OS 为 26 个月(95%CI,7.5-45)(p=0.34)。在利妥昔单抗治疗前组的中位淋巴瘤特异性生存期(LSS)为 30 个月(95%CI,8.0-52),利妥昔单抗治疗组的中位 LSS 为 36 个月(95%CI,16-158)(p=0.30)。当按化疗分层时,两个时代组的 OS 和 LSS 也没有显著差异。在多变量分析中,OS 和 LSS 均与淋巴瘤分期、保险状况和年龄相关,但与诊断时代或化疗无关。
心脏 DLBCL 罕见,主要影响老年人。年轻的年龄、局限性疾病分期、有医疗保险但无淋巴瘤诊断时代与更好的结局相关。