Plasma cell-free DNA is a prognostic biomarker for survival in patients with aggressive non-Hodgkin lymphomas

被引:20
作者
Hur, Joon Young [1 ,2 ]
Kim, Yeon Jeong [3 ]
Yoon, Sang Eun [1 ]
Son, Dae-Soon [4 ]
Park, Woong-Yang [3 ,5 ]
Kim, Seok Jin [1 ]
Park, Donghyun [3 ,6 ]
Kim, Won Seog [1 ]
机构
[1] Sungkyunkwan Univ, Samsung Med Ctr, Sch Med, Dept Med,Div Hematol Oncol, 81 Irwon Ro, Seoul 06351, South Korea
[2] Hanyang Univ, Guri Hosp, Dept Internal Med, Div Hematol & Oncol, Guri, South Korea
[3] Samsung Med Ctr, Samsung Genome Inst, 81 Irwon Ro, Seoul 06351, South Korea
[4] Hallym Univ, Data Sci Convergence Res Ctr, Sch Big Data Sci, Chunchon, South Korea
[5] Sungkyunkwan Univ, Sch Med, Dept Mol Cell Biol, Suwon, South Korea
[6] GENINUS Inc, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Cell-free DNA; Diffuse large B cell lymphoma; Aggressive T cell lymphoma; NK; T cell lymphoma; ABSOLUTE LYMPHOCYTE COUNT; FREE CIRCULATING DNA; CANCER-PATIENTS; MONOCYTE COUNT; DIAGNOSIS; PREDICTS; MARKER; RATIO; SERUM; MULTICENTER;
D O I
10.1007/s00277-020-04008-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cell-free DNA (cfDNA) can be released from tumor cells during proliferation and apoptosis; thus, a fraction of the cfDNA in patients with cancer is tumor-derived. However, the prognostic value of cfDNA in aggressive non-Hodgkin lymphoma (NHL) has not been determined. Between March 2017 and April 2019, plasma cfDNA was obtained from 158 patients with aggressive NHL who were registered in a prospective Samsung Medical Center lymphoma cohort (diffuse large B cell lymphoma (DLBCL), n = 51; T cell lymphoma (TCL), n = 51; NK/T cell lymphoma (NKTCL), n = 56). The concentration of cfDNA was estimated in longitudinal samples collected from patients with NHL before and during various chemotherapy regimens. In pretreatment samples, the median cfDNA concentration of all patients with aggressive lymphoma was 13.7 ng/dl (range 1.7-1792), which was significantly higher than that of healthy volunteers (median 7.4 ng, range 3.7-14.4, p < 0.001), and advanced stages showed a higher cfDNA level than earlier stages. Multivariate analysis identified high cfDNA as an independent factor for event-free survival that predicted poor prognosis in DLBCL (hazard ratio [HR] = 5.33, 95% confidence interval [CI] = 1.72-16.52, p = 0.003) and TCL (HR = 2.82, 95% CI = 1.10-7.20, p = 0.030). NKTCL patients with a high level of cfDNA had worse overall survival (HR = 4.71, 95% CI = 1.09-20.35, p = 0.037) compared with those with a low level of cfDNA. In this study, our results suggest the usefulness of pretreatment cfDNA as a prognostic marker for patients with DLBCL, TCL, and NKTCL.
引用
收藏
页码:1293 / 1302
页数:10
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