Department of Hematology Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research.
Division of Clinical Research, The Cancer Chemotherapy Center, Japanese Foundation for Cancer Research.
Biomed Res. 2022;43(4):99-106. doi: 10.2220/biomedres.43.99.
Cell-free DNA (cfDNA) is a fragment of DNA circulating in the blood, and its concentration is often elevated in cancer patients. To investigate the relationships between serum cfDNA concentration and clinical characteristics, including prognosis, we measured serum cfDNA concentration in 114 newly diagnosed lymphoma patients. The cfDNA concentrations in diffuse large B cell lymphoma (DLBCL) (62.5 ng/mL) and follicular lymphoma patients (51.6 ng/mL) were significantly elevated compared to healthy individuals (7.5 ng/mL, P < 0.001). In DLBCL, patients with elevated serum cfDNA (> 38.9 ng/mL) at diagnosis had significantly shorter time-to-progression compared to those without (P = 0.033). The addition of cfDNA concentration to the international prognostic index showed improved predictive power for time-to-progression. Moreover, cfDNA added significant prognostic value to other inflammatory markers such as B symptoms and sIL2R. There was a trend towards shorter progression-free survival and overall survival in patients with elevated cfDNA. Furthermore, B symptoms (P = 0.038), bulky masses (P = 0.031), non-GCB subtype (P = 0.012), and serum sIL-2R levels > 2,000 U/mL (P = 0.012) were associated with higher cfDNA levels. Our study showed that serum cfDNA concentration at diagnosis was associated with certain clinicopathological characteristics, and may be predictive of survival outcomes in DLBCL patients.
无细胞 DNA(cfDNA)是血液循环中游离的 DNA 片段,其浓度在癌症患者中通常升高。为了研究血清 cfDNA 浓度与临床特征(包括预后)之间的关系,我们在 114 名新诊断的淋巴瘤患者中测量了血清 cfDNA 浓度。弥漫性大 B 细胞淋巴瘤(DLBCL)(62.5ng/mL)和滤泡性淋巴瘤患者(51.6ng/mL)的 cfDNA 浓度明显高于健康个体(7.5ng/mL,P<0.001)。在 DLBCL 中,诊断时血清 cfDNA 升高(>38.9ng/mL)的患者与无升高的患者相比,进展时间明显缩短(P=0.033)。将 cfDNA 浓度加入国际预后指数后,对进展时间的预测能力得到了提高。此外,cfDNA 增加了其他炎症标志物如 B 症状和 sIL2R 的预后价值。cfDNA 升高的患者无进展生存期和总生存期有缩短的趋势。此外,B 症状(P=0.038)、大肿块(P=0.031)、非 GCB 亚型(P=0.012)和血清 sIL-2R 水平>2000U/mL(P=0.012)与更高的 cfDNA 水平相关。我们的研究表明,诊断时血清 cfDNA 浓度与某些临床病理特征相关,可能预测 DLBCL 患者的生存结局。