Cho Hyunsoo, Kim Se Hoon, Kim Soo-Jeong, Chang Jong Hee, Yang Woo Ick, Suh Chang-Ok, Cheong June-Won, Kim Yu Ri, Lee Jung Yeon, Jang Ji Eun, Kim Yundeok, Min Yoo Hong, Kim Jin Seok
Division of Hematology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul, 03722, South Korea.
Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, South Korea.
Ann Hematol. 2017 Jul;96(7):1163-1173. doi: 10.1007/s00277-017-3014-x. Epub 2017 May 15.
The prognostic role of CD68 and FoxP3 in primary central nervous system lymphoma (PCNSL) has not been evaluated. Thus, we examined the prognostic significance of CD68 and FoxP3 expression in tumor samples of 76 newly diagnosed immunocompetent PCNSL patients. All patients were treated initially with high-dose methotrexate (HD-MTX)-based chemotherapy, and 16 (21.1%) patients received upfront autologous stem cell transplantation (ASCT) consolidation. High expression of CD68 (>55 cells/high-power field) or FoxP3 (>15 cells/high-power field) was observed in 10 patients, respectively. High CD68 expression was associated with inferior overall survival (OS) and progression-free survival (PFS) in multivariate analysis (P = 0.023 and P = 0.021, respectively). In addition, we performed subgroup analysis based on upfront ASCT. High CD68 expression was also associated with inferior OS and PFS in multivariate analysis (P = 0.013 and P < 0.001, respectively) among patients who did not receive upfront ASCT (n = 60), but not in patients who received upfront ASCT. The expression of FoxP3 was not significantly associated with survival. Therefore, we identified a prognostic significance of high CD68 expression in PCNSL, which suggests a need for further clinical trials and biological studies on the role of PCNSL tumor microenvironment.
CD68和FoxP3在原发性中枢神经系统淋巴瘤(PCNSL)中的预后作用尚未得到评估。因此,我们检测了76例新诊断的免疫功能正常的PCNSL患者肿瘤样本中CD68和FoxP3表达的预后意义。所有患者最初均接受基于大剂量甲氨蝶呤(HD-MTX)的化疗,16例(21.1%)患者接受了前期自体干细胞移植(ASCT)巩固治疗。分别在10例患者中观察到CD68(>55个细胞/高倍视野)或FoxP3(>15个细胞/高倍视野)的高表达。在多因素分析中,CD68高表达与总生存期(OS)和无进展生存期(PFS)较差相关(分别为P = 0.023和P = 0.021)。此外,我们根据前期ASCT进行了亚组分析。在未接受前期ASCT的患者(n = 60)中,多因素分析显示CD68高表达也与较差的OS和PFS相关(分别为P = 0.013和P < 0.001),但在接受前期ASCT的患者中并非如此。FoxP3的表达与生存率无显著相关性。因此,我们确定了PCNSL中CD68高表达的预后意义,这表明需要对PCNSL肿瘤微环境的作用进行进一步的临床试验和生物学研究。