Wang Xin, Liu Xin, Zhong Qiu-Zi, Wu Tao, Wu Yun-Peng, Yang Yong, Chen Bo, Jing Hao, Tang Yuan, Jin Jing, Liu Yue-Ping, Song Yong-Wen, Fang Hui, Lu Ning-Ning, Li Ning, Zhai Yi-Rui, Zhang Wen-Wen, Wang Shu-Lian, Chen Fan, Qi Shu-Nan, Li Ye-Xiong
Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences (CAMS) and Peking Union Medical College (PUMC), Collaborative Innovation Center for Cancer Medicine, Beijing 100021, China.
Beijing Hospital, National Geriatric Medical Center, Beijing, China.
Radiother Oncol. 2023 Nov;188:109902. doi: 10.1016/j.radonc.2023.109902. Epub 2023 Sep 9.
We aimed to investigate the incidence of lymphoma-related death (LRD) and the long-term net survival benefit of radiotherapy (RT) for early-stage diffuse large B-cell lymphoma (DLBCL) in the rituximab era.
10,841 adults diagnosed with early-stage DLBCL between 2002-2015 were retrospectively analyzed using data from the Surveillance, Epidemiology, and End Results database. Primary therapy was categorized into combined-modality treatment (CMT, n = 3,631) and chemotherapy alone (n = 7,210). Competing risk analysis was used to evaluate the cumulative incidence of mortality. Inverse probability of treatment weighting (IPTW) was used to balance groups. The net survival benefit of RT was estimated through relative survival (RS), standardized mortality ratio (SMR), and transformed Cox regression, while controlling for background mortality.
Patients initially treated with CMT had a lower cumulative incidence of LRD compared to those who received chemotherapy alone (HR 0.63, 95%CI: 0.57-0.69; P < 0.001). The 10-year overall survival (OS), RS, and SMR for CMT were 66.1%, 85.0%, and 1.71 respectively, which were significantly better than those for chemotherapy alone (53.0%; 69.8%; 2.62; all P < 0.001). IPTW and multivariable analysis revealed that the addition of RT led to better OS (HR 0.67, 95%CI: 0.62-0.71; P < 0.001) and RS (HR 0.69, 95%CI: 0.65-0.74; P < 0.001). Moreover, compared with chemotherapy alone, the benefit of OS and RS for CMT increased over time within 10 years of diagnosis.
RT reduced LRD and improved the long-term net survival in early-stage DLBCL in the rituximab era. Further prospective studies are warranted to assess the specific patient population that would benefit the most from consolidative RT in early-stage DLBCL.
我们旨在调查利妥昔单抗时代早期弥漫性大B细胞淋巴瘤(DLBCL)的淋巴瘤相关死亡(LRD)发生率以及放疗(RT)的长期净生存获益。
利用监测、流行病学和最终结果数据库的数据,对2002年至2015年间诊断为早期DLBCL的10841名成年人进行回顾性分析。初始治疗分为综合治疗(CMT,n = 3631)和单纯化疗(n = 7210)。采用竞争风险分析评估死亡率的累积发生率。使用治疗权重逆概率(IPTW)来平衡各组。在控制背景死亡率的同时,通过相对生存(RS)、标准化死亡率比值(SMR)和转换后的Cox回归估计RT的净生存获益。
与单纯接受化疗的患者相比,初始接受CMT治疗的患者LRD累积发生率更低(风险比0.63,95%置信区间:0.57 - 0.69;P < 0.001)。CMT的10年总生存(OS)、RS和SMR分别为66.1%、85.0%和1.71,显著优于单纯化疗(53.0%;69.8%;2.62;所有P < 0.001)。IPTW和多变量分析显示,添加RT可带来更好的OS(风险比0.67,95%置信区间:0.62 - 0.71;P < 0.001)和RS(风险比0.69,95%置信区间:0.65 - 0.74;P < 0.001)。此外,与单纯化疗相比,CMT在诊断后的10年内OS和RS的获益随时间增加。
在利妥昔单抗时代,RT降低了早期DLBCL的LRD并改善了长期净生存。有必要进行进一步的前瞻性研究,以评估在早期DLBCL中从巩固性RT中获益最大的特定患者群体。