利妥昔单抗时代原发性咽淋巴环弥漫大 B 细胞淋巴瘤放疗临床获益降低。
Reduced radiotherapy clinical benefit for primary Waldeyer's ring diffuse large B-cell lymphoma in the rituximab era.
机构信息
Departments of Lymphoma, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center of Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, the Sino-US Center for Lymphoma and Leukemia Research, Tianjin, China.
Departments of Immunology/Biotherapy, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China.
出版信息
Hematol Oncol. 2021 Oct;39(4):490-497. doi: 10.1002/hon.2869. Epub 2021 Apr 27.
This study aimed to identify the prognostic factors in patients with Waldeyer's ring diffuse large B-cell lymphoma (WR-DLBCL), comparing the efficacy of radiotherapy (RT) for the WR-DLBCL patients in the pre-rituximab and rituximab eras. We conducted a retrospective analysis of 134 patients diagnosed with WR-DLBCL. Univariate and multivariate analyses were performed to identify the prognostic factors for WR-DLBCL. Then, we divided these patients into the rituximab plus chemotherapy group (R-chemotherapy) (n = 88) and chemotherapy group (n = 46), and the Kaplan-Meier and Cox regression model analyses were applied to investigate the treatment value of RT in both the groups. Multivariate analysis revealed international prognostic index (IPI) ≥ 3 and chemotherapy without rituximab as significant risk factors for the progression-free survival (PFS, IPI ≥ 3: p = 0.001; chemotherapy without rituximab: p = 0.002) and overall survival (OS, IPI ≥ 3, p < 0.001; chemotherapy without rituximab, p = 0.024). Rituximab combined with chemotherapy significantly improved PFS (p = 0.002) and OS (p = 0.006) in these patients. RT did not significantly contribute to the survival in the overall cohort analysis, whereas in the subgroup analysis, RT significantly improved the PFS (p = 0.025) and OS (p = 0.029) for the patients in the chemotherapy group, but not in the R-chemotherapy group. In conclusion, the WR-DLBCL patients could benefit from RT in the pre-rituximab era, whereas the addition of rituximab to chemotherapy significantly improved the survival of WR-DLBCL patients, and the clinical benefit of RT was reduced.
这项研究旨在确定瓦尔德环弥漫性大 B 细胞淋巴瘤(WR-DLBCL)患者的预后因素,并比较在利妥昔单抗前和利妥昔单抗时代接受放疗(RT)治疗 WR-DLBCL 患者的疗效。我们对 134 例诊断为 WR-DLBCL 的患者进行了回顾性分析。采用单因素和多因素分析确定 WR-DLBCL 的预后因素。然后,我们将这些患者分为利妥昔单抗联合化疗组(R-化疗组)(n=88)和化疗组(n=46),并应用 Kaplan-Meier 和 Cox 回归模型分析来探讨 RT 在两组中的治疗价值。多因素分析显示国际预后指数(IPI)≥3 和无利妥昔单抗的化疗是无进展生存(PFS,IPI≥3:p=0.001;无利妥昔单抗的化疗:p=0.002)和总生存(OS,IPI≥3,p<0.001;无利妥昔单抗的化疗,p=0.024)的显著危险因素。利妥昔单抗联合化疗显著改善了这些患者的 PFS(p=0.002)和 OS(p=0.006)。在总体队列分析中,RT 对生存没有显著贡献,但在亚组分析中,RT 显著改善了化疗组患者的 PFS(p=0.025)和 OS(p=0.029),但对 R-化疗组患者没有改善。总之,WR-DLBCL 患者在前利妥昔单抗时代可以从 RT 中获益,而利妥昔单抗联合化疗可显著改善 WR-DLBCL 患者的生存,RT 的临床获益降低。