Wang Jingnan, Liu Xin, Wu Yunpeng, Zhong Qiuzi, Wu Tao, Yang Yong, Chen Bo, Jing Hao, Tang Yuan, Jin Jing, Liu Yueping, Song Yongwen, Fang Hui, Lu Ningning, Li Ning, Zhai Yirui, Zhang Wenwen, Deng Min, Wang Shulian, Chen Fan, Yin Lin, Hu Chen, Qi Shunan, Li Yexiong
Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Collaborative Innovation Center for Cancer Medicine, Beijing, China.
Beijing Hospital, National Geriatric Medical Center, Beijing, China.
J Natl Cancer Cent. 2024 Apr 23;4(3):249-259. doi: 10.1016/j.jncc.2024.04.002. eCollection 2024 Sep.
To evaluate whether improved progression-free survival (PFS) from radiotherapy (RT) translates into an overall survival (OS) benefit for diffuse large B-cell lymphoma (DLBCL).
A systematic literature search identified randomized controlled trials (RCTs) and retrospective studies that compared combined-modality therapy (CMT) with chemotherapy (CT) alone. Weighted regression analyses were used to estimate the correlation between OS and PFS benefits. Cohen's kappa statistic assessed the consistency between DLBCL risk-models and PFS patterns. Furthermore, the benefit trend of RT was analyzed by fitting a linear regression model to the pooled hazard ratio (HR) according to the PFS patterns.
For both 7 RCTs and 52 retrospective studies, correlations were found between PFS HR (HR) and OS HR (HR) at trial level ( = 0.639-0.876), and between PFS and OS rates at treatment-arm level, regardless of CT regimens ( = 0.882-0.964). Incorporating RT into CT increased about 18% of PFS, and revealed a different OS benefit profile. Patients were stratified into four CT-generated PFS patterns (>80%, >60-80%, >40-60%, and ≤40%), which was consistent with risk-stratified subgroups (kappa > 0.6). Absolute gain in OS from RT ranged from ≤5% at PFS >80% to about 21% at PFS ≤40%, with pooled HR from 0.70 (95% CI, 0.51-0.97) to 0.48 (95% CI, 0.36-0.63) after rituximab-based CT. The OS benefit of RT was predominant in intermediate- and high-risk patients with PFS ≤ 80%.
We demonstrated a varied OS benefit profile of RT to inform treatment decisions and clinical trial design.
评估放射治疗(RT)带来的无进展生存期(PFS)改善是否能转化为弥漫性大B细胞淋巴瘤(DLBCL)的总生存期(OS)获益。
系统文献检索确定了比较联合治疗(CMT)与单纯化疗(CT)的随机对照试验(RCT)和回顾性研究。采用加权回归分析估计OS和PFS获益之间的相关性。Cohen's kappa统计量评估DLBCL风险模型与PFS模式之间的一致性。此外,根据PFS模式,通过对汇总风险比(HR)拟合线性回归模型来分析RT的获益趋势。
对于7项RCT和52项回顾性研究,在试验水平上发现PFS风险比(HR)与OS风险比(HR)之间存在相关性(=0.639 - 0.876),且在治疗组水平上PFS与OS率之间也存在相关性,无论CT方案如何(=0.882 - 0.964)。将RT纳入CT可使PFS提高约18%,并显示出不同的OS获益情况。患者被分为四种由CT产生的PFS模式(>80%、>60 - 80%、>40 - 60%和≤40%),这与风险分层亚组一致(kappa>0.6)。RT带来的OS绝对获益范围从PFS>80%时的≤5%到PFS≤40%时的约21%,在基于利妥昔单抗的CT治疗后,汇总HR从0.70(95%CI,0.51 - 0.97)到0.48(95%CI,0.36 - 0.63)。RT的OS获益在PFS≤80%的中高危患者中占主导地位。
我们证明了RT具有不同的OS获益情况,可为治疗决策和临床试验设计提供参考。