不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A retrospective analysis of EBV-DNA status with the prognosis of lymphoma.
A retrospective analysis of EBV-DNA status with the prognosis of lymphoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
已有证据表明,EB病毒(EBV)感染与淋巴瘤的临床病理特征相关,但治疗后EBV-DNA状态与预后的关系所知甚少。本研究采用实时定量聚合酶链反应(PCR),检测全部26,527例淋巴瘤患者外周血中的EBV-DNA载量,并回顾性分析202例患者的临床特征及预后,其中100例EBV-DNA阳性,另随机选择102例阴性患者。淋巴瘤患者EBV-DNA平均阳性率为0.376%。与阴性患者相比,EBV-DNA阳性患者更常伴乳酸脱氢酶(LDH)和β₂微球蛋白(β₂-MG)升高、B症状及继发性噬血细胞综合征,客观缓解率也较低。多变量分析显示,EBV-DNA阳性患者的无进展生存期(PFS)和总生存期(OS)较差;在T/NK细胞淋巴瘤中,治疗前EBV-DNA水平与PFS相关,但与OS无关。对于T/NK细胞淋巴瘤,治疗后EBV-DNA转阴与较好的PFS相关,但与OS无关;与CHOP方案治疗相比,二线治疗更容易使EBV-DNA转阴。
综上,治疗前EBV-DNA阳性可作为反映肿瘤负荷的生物标志物,也是独立预后因素。治疗后EBV-DNA转阴则是T/NK细胞淋巴瘤的良好预后因素。
Epstein-Barr virus (EBV) infection is proved to be associated with clinicopathology of lymphoma.
However, little is known about the relationship between EBV-DNA status after treatment and prognosis. In this study, real-time polymerase chain reaction (PCR) was used for quantitative detection of EBV-DNA load in peripheral blood of all 26,527 patients with lymphoma, and the clinical characteristics and prognosis of 202 patients were retrospectively analysed, including 100 patients with positive EBV-DNA and 102 randomly selected patients with negative EBV-DNA.
We found that the average rate of EBV-DNA positivity in lymphomas was 0. 376%, and EBV-DNA-positive patients presented higher risk with elevated lactate dehydrogenase (LDH) and 2-MG level, B symptoms, secondary hemophagocytic syndrome and lower objective response rate compared to EBV-DNA-negative patients. Multivariate analysis revealed EBV-DNA-positive patients had inferior progression-free survival (PFS) and overall survival (OS) and EBV-DNA level before treatment was related to PFS but not OS of T/NK cell lymphoma.
In T/NK cell lymphoma, EBV-DNA converting negative after treatment was correlated with better PFS but not OS, and second-line therapy could induce more EBV-DNA-negative conversion compared to CHOP-based therapy. In all, EBV-DNA positivity before treatment can be a biomarker representing the tumour burden and an independent prognostic factor. EBV-DNA-negative conversion after treatment is a good prognostic factor for T/NK cell lymphomas.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。