术前血清和尿液CCL27在预测非肌层浸润性膀胱癌患者复发和进展风险中的作用
Role of preoperative serum and urine CCL27 in predicting the risk of recurrence and progression in patients with non-muscle invasive bladder cancer
投稿时间:2024-09-18  修订日期:2024-10-29
DOI:
中文关键词:  CCL27  非肌层浸润性膀胱癌  复发  进展
英文关键词:CCL27  non-muscle invasive bladder cancer  recurrence  progression
基金项目:咸阳市重点研发计划(S2022-ZDYF-SF-1062)
作者单位邮编
任磊* 咸阳市第一人民医院 712000
王亚辉 咸阳市第一人民医院 
韩明 咸阳市第一人民医院 
施量 咸阳市第一人民医院 
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中文摘要:
      目的 探讨术前血清和尿液趋化因子配体27(CCL27)在预测非肌层浸润性膀胱癌(NMIBC)患者复发和进展风险中的作用。方法 2017年9月10日至2019年4月1日,从医院泌尿外科共招募15例接受经尿道膀胱肿瘤切除术(TURBT)的NMIBC患者作为发现组,91例成功行TURBT的NMIBC患者作为验证组,采集术前血清和尿液样本。发现组细胞因子/趋化因子通过多重分析技术检测。验证组血清和尿液CCL27水平通过酶联免疫吸附试验法检测。结果 在发现组中,复发与无复发或进展与无进展患者仅在CCL27水平上有显著差异(P<0.05)。在验证组中,复发/进展组术前血清和尿液CCL27水平显著高于无复发/无进展组(P<0.05)。血清和尿液CCL27水平预测NMIBC复发的ROC曲线下面积(AUC)分别为0.780(95%CI:0.678~0.881)、0.869(95%CI:0.796~0.942);预测NMIBC进展的AUC分别为0.803(95%CI:0.708~0.897)、0.862(95%CI:0.788~0.936)。Logistic回归分析显示术前尿液CCL27高水平是影响NMIBC复发或进展的独立预测因子(P<0.05)。根据ROC曲线确定的截断值将NMIBC患者分为血清或尿液CCL27高水平组和低水平组。随访5年期间,血清和尿液CCL27高水平组患者中位无复发生存期(RFS)和中位无进展生存期(PFS)明显更短(P<0.001)。结论 CCL27水平上调与NMIBC复发和进展密切相关,术前血清和尿液CCL27有希望作为识别NMIBC复发和进展高风险患者的早期预测标志物,而且尿液CCL27的预测效能更优。
英文摘要:
      Objective To investigate the role of preoperative serum and urine chemokine ligand 27 (CCL27) in predicting the risk of recurrence and progression in patients with non-muscle invasive bladder cancer (NMIBC). Methods From September 10, 2017 to April 1, 2019, a total of 15 NMIBC patients with transurethral resection of bladder tumor (TURBT) were recruited from the Department of Urology of the hospital as the discovery group, and 91 NMIBC patients with successful TURBT were recruited as the validation group, and preoperative serum and urine samples were collected. Discovery group cytokines/chemokines were detected by flexible Multi-Analyte Profiling. Serum and urine CCL27 levels in the validation group were detected by enzyme-linked immunosorbent assay. Results In the discovery group, there were significant differences between patients with recurrence and those without recurrence, or between patients with progression and those without progression only at the level of CCL27 (P<0.05). In the verification group, the preoperative serum and urine CCL27 levels in the relapsing/progressing group were significantly higher than those in the non-relapsing/progressing group (P<0.05). The area under ROC curve (AUC) of serum and urine CCL27 for predicting NMIBC recurrence were 0.780 (95%CI: 0.678~0.881) and 0.869 (95%CI: 0.796~0.942), which predicting the progression of NMIBC were 0.803 (95%CI: 0.708~0.897) and 0.862 (95%CI: 0.788~0.936), respectively. Logistic regression analysis showed that preoperative high urinary CCL27 level was an independent predictor of recurrence or progression of NMIBC (P<0.05). According to the cut-off value determined by the ROC curve, NMIBC patients were divided into groups with high serum or urine CCL27 level and groups with low serum or urine CCL27 level. During 5-year follow-up, median relapse-free survival (RFS) and median progression-free survival (PFS) were significantly shorter in patients with high serum and urine CCL27 levels (P<0.001). Conclusion Upregulation of CCL27 level is closely related to the recurrence and progression of NMIBC. Preoperative serum or urine CCL27 is promising as an early predictor for identifying patients at high risk of recurrence and progression of NMIBC, while the predictive value of urine CCL27 is better.
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