Department of Medicine, Lymphoma Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.
Blood Adv. 2023 Sep 12;7(17):4838-4847. doi: 10.1182/bloodadvances.2022009587.
Nodal marginal zone lymphoma (NMZL) is a rare non-Hodgkin B-cell lymphoma that has historically been difficult to define, though is now formally recognized by the World Health Organization Classification. To better characterize the clinical outcomes of patients with NMZL, we reviewed a sequential cohort of 187 patients with NMZL to describe baseline characteristics, survival outcomes, and time-to-event data. Initial management strategies were classified into five categories: observation, radiation, anti-CD20 monoclonal antibody therapy, chemoimmunotherapy, or other. Baseline Follicular Lymphoma International Prognostic Index scores were calculated to evaluate prognosis. A total of 187 patients were analyzed. The five-year overall survival was 91% (95% confidence interval [CI], 87-95), with a median follow-up time of 71 months (range, 8-253) among survivors. A total of 139 patients received active treatment at any point, with a median follow-up time of 56 months (range, 13-253) among survivors who were never treated. The probability of remaining untreated at five years was 25% (95% CI, 19-33). For those initially observed, the median time to active treatment was 72 months (95% CI, 49-not reached). For those who received at least one active treatment, the cumulative incidence of receiving a second active treatment at 60 months was 37%. Transformation to large B-cell lymphoma was rare, with a cumulative incidence of 15% at 10 years. In summary, our series is a large cohort of uniformly diagnosed NMZL with detailed analyses of survival and time to event analyses. We showed that NMZL commonly presents as an indolent lymphoma for which initial observation is often a reasonable strategy.
结外边缘区 B 细胞淋巴瘤(NMZL)是一种罕见的非霍奇金 B 细胞淋巴瘤,过去难以定义,但现在已被世界卫生组织分类正式认可。为了更好地描述 NMZL 患者的临床结局,我们回顾性分析了 187 例 NMZL 患者的连续队列,以描述基线特征、生存结局和时间事件数据。初始治疗策略分为五类:观察、放疗、抗 CD20 单克隆抗体治疗、化疗免疫治疗或其他。计算滤泡性淋巴瘤国际预后指数评分以评估预后。共分析了 187 例患者。五年总生存率为 91%(95%置信区间[CI],87-95),幸存者中位随访时间为 71 个月(范围,8-253)。共有 139 例患者在任何时间接受了积极治疗,幸存者的中位随访时间为 56 个月(范围,13-253),从未接受过治疗。五年未接受治疗的概率为 25%(95%CI,19-33)。对于最初观察的患者,中位时间至积极治疗为 72 个月(95%CI,49-未达到)。对于接受至少一种积极治疗的患者,60 个月时接受第二种积极治疗的累积发生率为 37%。向大 B 细胞淋巴瘤转化罕见,10 年内累积发生率为 15%。总之,我们的系列是一个大型的 NMZL 患者队列,对生存和时间事件进行了详细分析。我们表明,NMZL 通常表现为惰性淋巴瘤,初始观察通常是一种合理的策略。