Fujian Medical University Union Hospital, Fujian Provincial Key Laboratory on Hematology, Fujian Institute of Hematology, Fuzhou, Fujian, China.
J Cancer Res Clin Oncol. 2023 Jun;149(6):2311-2318. doi: 10.1007/s00432-022-04381-8. Epub 2022 Oct 11.
This single-centre study aimed to determine the clinicopathological characteristics and prognosis for patients with co-existing FL and DLBCL components (FL/DLBCL).
We retrospectively analysed the clinical characteristics and prognosis of patients diagnosed with FL/DLBCL (n = 56) and with pure FL (n = 260) or de novo DLBCL (n = 812) (controls) between January 2013 and December 2021.
The median age of patients with FL/DLBCL was 52 years. The amount of the DLBCL component ranged from 5 to 95%. Among the 56 FL/DLBCL cases analysed, 67.9% were of germinal centre B-cell (GCB) origin, 26.8% non-GCB origin, and 5.3% were unclassified. The clinical features of patients with FL/DLBCL were intermediate, falling between those of FL and DLBCL. Propensity-score matching was performed for patients with similar baseline characteristics who were receiving the rituximab plus cyclophosphamide, doxorubicin or epirubicin, vindesine, and prednisone (R-CHOP) regimen. Patients with FL/DLBCL showed inferior outcomes compared to those with FL, with a lower complete remission (CR) rate, progression-free survival (PFS), and overall survival (OS). Bone marrow involvement and B symptoms were identified as independent adverse prognostic factors for PFS among patients with FL/DLBCL. Patients with FL/DLBCL presented a lower CR rate and PFS but similar OS to those with DLBCL when receiving the R-CHOP regimen.
Patients with FL/DLBCL showed inferior treatment response and survival than those with pure FL and had a lower CR rate and PFS, but similar OS to those with DLBCL in the rituximab era.
本单中心研究旨在确定同时存在滤泡性淋巴瘤(FL)和弥漫性大 B 细胞淋巴瘤(DLBCL)成分的患者的临床病理特征和预后(FL/DLBCL)。
我们回顾性分析了 2013 年 1 月至 2021 年 12 月期间诊断为 FL/DLBCL(n=56)、单纯 FL(n=260)或初发 DLBCL(n=812)(对照组)的患者的临床特征和预后。
FL/DLBCL 患者的中位年龄为 52 岁。DLBCL 成分的数量范围为 5%至 95%。在分析的 56 例 FL/DLBCL 病例中,67.9%为生发中心 B 细胞(GCB)起源,26.8%为非 GCB 起源,5.3%为未分类。FL/DLBCL 患者的临床特征处于 FL 和 DLBCL 之间的中间水平。对接受利妥昔单抗联合环磷酰胺、多柔比星或表柔比星、长春碱和泼尼松(R-CHOP)方案且基线特征相似的患者进行倾向评分匹配。与 FL 患者相比,FL/DLBCL 患者的结局较差,完全缓解(CR)率、无进展生存期(PFS)和总生存期(OS)较低。骨髓受累和 B 症状被确定为 FL/DLBCL 患者 PFS 的独立不良预后因素。在接受 R-CHOP 方案治疗时,FL/DLBCL 患者的 CR 率和 PFS 较低,但 OS 与 DLBCL 患者相似。
在利妥昔单抗时代,与单纯 FL 患者相比,FL/DLBCL 患者的治疗反应和生存较差,CR 率和 PFS 较低,但与 DLBCL 患者的 OS 相似。