Departments of Oncology and Medicine, University of Calgary, Tom Baker Cancer Centre, Calgary, AB, Canada.
Department of Medical Oncology, University of Alberta, Cross Cancer Institute, Edmonton, AB, Canada.
Clin Lymphoma Myeloma Leuk. 2018 Dec;18(12):829-835. doi: 10.1016/j.clml.2018.08.015. Epub 2018 Aug 29.
Patients with low tumor burden follicular lymphoma (FL) are commonly managed with watchful waiting (WW). The incidence of organ dysfunction and/or transformation at disease progression, and subsequent impact on outcomes is poorly understood.
Patients managed with WW during 1994 to 2011 were identified through the Alberta Lymphoma Database. Individuals receiving immediate rituximab (R)-chemotherapy were identified as a comparator group to those on WW who received R-chemotherapy at progression. Endpoints included transformation, organ dysfunction, time to progression, time to next treatment, progression-free survival (PFS) after chemotherapy, and overall survival (OS).
We identified 238 patients managed with WW (28.9% of registry patients) during this 17-year period. The median follow up was 8.2 years. At a median of 29.9 months, 58 (24.4%) of these patients developed organ dysfunction and/or transformation. Of 169 (71%) patients who required therapy, 10-year OS was inferior for those with transformation (hazard ratio, 2.88; P = .002) and organ dysfunction (hazard ratio, 2.10; P = .028). PFS after R-chemotherapy and OS in patients without organ dysfunction and/or transformation was not affected by the initial WW period, compared with immediate R-chemotherapy. WW resulted in increased high risk FL International Prognostic Index scores at initiation of R-chemotherapy (45% vs. 20%), and more frequent transformation at progression (5-year risk, 17.8% vs. 3.5%; P < .001). Baseline characteristics did not predict organ dysfunction.
Patients with FL accepting initial WW should be aware of the 1 in 4 risk of organ dysfunction and/or transformation, and subsequent inferior OS. Physicians should consider surveillance for progression to consider early therapy.
低肿瘤负荷滤泡性淋巴瘤(FL)患者通常采用观察等待(WW)治疗。疾病进展时器官功能障碍和/或转化的发生率及其对预后的后续影响尚不清楚。
通过艾伯塔淋巴瘤数据库确定了 1994 年至 2011 年期间接受 WW 治疗的患者。将立即接受利妥昔单抗(R)化疗的个体确定为与 WW 组的比较,后者在进展时接受 R 化疗。终点包括转化、器官功能障碍、进展时间、下一次治疗时间、化疗后无进展生存期(PFS)和总生存期(OS)。
我们在这 17 年期间确定了 238 例接受 WW 治疗的患者(登记患者的 28.9%)。中位随访时间为 8.2 年。在中位 29.9 个月时,这些患者中有 58 例(24.4%)出现器官功能障碍和/或转化。在需要治疗的 169 例(71%)患者中,转化患者的 10 年 OS 较差(危险比,2.88;P=.002)和器官功能障碍(危险比,2.10;P=.028)。与立即接受 R 化疗相比,无器官功能障碍和/或转化的患者在接受 R 化疗后的 PFS 和 OS 不受初始 WW 期间的影响。WW 导致 R 化疗起始时高风险 FL 国际预后指数评分增加(45% vs. 20%),进展时转化更频繁(5 年风险,17.8% vs. 3.5%;P<.001)。基线特征不能预测器官功能障碍。
接受初始 WW 的 FL 患者应意识到 1/4 的器官功能障碍和/或转化风险,以及随后的 OS 较差。医生应考虑进行进展监测,以考虑早期治疗。