Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Cancer Res Treat. 2021 Jul;53(3):847-856. doi: 10.4143/crt.2020.1060. Epub 2020 Dec 17.
We aimed to investigate the prognostic value of serum β2-microglobulin for patients with Burkitt lymphoma (BL) and to propose a risk-stratifying classification system.
A prospective registry-based cohort study of BL patients treated with dose-intensive or effective dose-adjusted chemotherapies (n=81) was conducted. Survival outcomes were compared based on previously reported risk groups and/or serum β2-microglobulin levels. A risk-stratifying classification system incorporating serum β2-microglobulin levels was proposed and validated in an independent validation cohort (n=60).
The median age was 47 years, and 57 patients (70.4%) were male. Patients with high serum β2-microglobulin levels (> 2 mg/L) had significantly worse progression-free survival (PFS) and overall survival (OS) (p < 0.01 for both). Serum β2-microglobulin levels further stratified patients in the low-risk and high-risk groups in terms of PFS (p=0.010 and p=0.044, respectively) and OS (p=0.014 and p=0.026, respectively). Multivariate analyses revealed that a high serum β2-microglobulin level (> 2 mg/L) was independently associated with a shorter PFS (hazards ratio [HR], 3.56; p=0.047) and OS (HR, 4.66; p=0.043). The new classification system incorporating the serum β2-microglobulin level allowed the stratification of patients into three distinct risk subgroups with 5-year OS rates of 100%, 89.5%, and 62.5%. In an independent cohort of BL, the system was validated by stratifying patients with different survival outcomes.
Serum β2-microglobulin level is an independent prognostic factor for BL patients. The proposed β2-microglobulin-based classification system could stratify patients with distinct survival outcomes, which may help define appropriate treatment approaches for individual patients.
本研究旨在探讨血清β2-微球蛋白(β2-MG)对伯基特淋巴瘤(BL)患者的预后价值,并提出一种风险分层分类系统。
本研究为前瞻性基于登记的 BL 患者队列研究,纳入接受剂量密集或有效剂量调整化疗的患者(n=81)。根据先前报道的风险组和/或血清β2-MG 水平比较生存结果。在独立验证队列(n=60)中提出并验证了一种纳入血清β2-MG 水平的风险分层分类系统。
中位年龄为 47 岁,57 例(70.4%)为男性。血清β2-MG 水平较高(>2mg/L)的患者无进展生存期(PFS)和总生存期(OS)显著更差(均 p<0.01)。血清β2-MG 水平进一步分层了低危和高危组患者的 PFS(p=0.010 和 p=0.044)和 OS(p=0.014 和 p=0.026)。多变量分析显示,高血清β2-MG 水平(>2mg/L)与较短的 PFS(危险比[HR],3.56;p=0.047)和 OS(HR,4.66;p=0.043)独立相关。纳入血清β2-MG 水平的新分类系统可将患者分为三个不同的风险亚组,5 年 OS 率分别为 100%、89.5%和 62.5%。在 BL 的独立队列中,该系统通过分层不同生存结局的患者得到验证。
血清β2-MG 水平是 BL 患者的独立预后因素。提出的基于β2-MG 的分类系统可分层具有不同生存结局的患者,这可能有助于为个体患者确定合适的治疗方法。