临床肿瘤学杂志

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晚期胰腺癌患者血清C反应蛋白水平动态变化与化疗疗效及预后的关系分析

杨佳程1,蔡 讯2,宋卫峰2,王理伟2

  

  1. 1 215200 江苏苏州 吴江区第一人民医院肿瘤内科2 200080 上海交通大学附属第一人民医院肿瘤科
  • 收稿日期:2014-08-12 修回日期:2014-10-04 出版日期:2014-12-31 发布日期:2014-12-31
  • 通讯作者: 王理伟

The relationship between C-reactive protein kinetics and efficacy, prognosis of patients with advanced pancreatic cancer

YANG Jiacheng, CAI Xun, SONG Weifeng, WANG Liwei.

  

  1. Department of Oncology, the First Peoples Hospital of Wujiang, Suzhou 215200, China
  • Received:2014-08-12 Revised:2014-10-04 Online:2014-12-31 Published:2014-12-31
  • Contact: WANG Liwei

摘要: 目的 探讨血清C反应蛋白(CRP)动态变化与晚期胰腺癌一线化疗疗效及预后的关系。方法 根据基线CRP水平和一线化疗过程中CRP动态变化将上海交通大学胰腺癌诊治中心2008年12月至2013年12月收治的61例晚期胰腺癌患者分为4组:A1组20例,CRP基线水平升高(≥5mg/L)且化疗过程中维持高水平;A2组11例,CRP基线水平升高且化疗过程中至少1次恢复正常(<5mg/L);B1组17例,CRP基线水平正常且化疗过程中至少1次升高;B2组13例,CRP基线水平正常且化疗过程中维持正常。采用RECIST 1.1标准评价疗效,随访生存资料并分析患者预后情况,采用Cox比例风险回归模型分析影响晚期胰腺癌一线化疗预后的独立因素。结果 61例患者均可评价疗效,无获CR者,其中PR 6例,SD 25例,PD 30例,疾病控制率(DCR)为50.82%;截止2013年12月31日,死亡54例,存活7例,中位生存期(OS)为7.20个月,中位无进展生存期(PFS)为3.03个月;A1、A2、B1、B2组的DCR分别为35.0%、54.6%、41.2%和84.6%,中位OS分别为4.97、8.87、7.20、10.47个月,中位PFS分别为1.97、3.83、3.20、6.90个月,以上差异均有统计学意义(P<0.05);Cox多因素分析结果显示,基线CRP、CRP动态变化、白蛋白及CA19-9水平为影响晚期胰腺癌预后的独立因素。结论 CRP可作为判断晚期胰腺癌患者临床预后的标志之一,基线CRP水平和一线化疗过程中CRP动态变化是晚期胰腺癌患者的独立预后因素。

Abstract: Objective To investigate the relationship between C-reactive protein(CRP) kinetics and efficacy of the first-line chemotherapy and prognosis, as to analyze whether CRP can be one of the biological markers indicating the clinical prognosis of advanced pancreatic cancer. Methods Sixty-one patients with advanced pancreatic cancer in dignosis and treatment center of pancreatic cancer affiliated to Shanghai Jiaotong university from December 2008 to December 2013 were enrolled in this study. The 61 cases were assigned into four groups according to baseline CRP and CRP kinetics: group A1, patients whose baseline CRP≥5mg/L and never normalized(CRP<5mg/L) during treatment; group A2, patients whose baseline CRP≥5mg/L and normalized at least one time during treatment; group B1, patients whose baseline CRP<5mg/L and elevated(CRP≥5mg/L) at least one time during treatment and group B2, patients whose baseline CRP<5mg/L and never elevated during treatment. The RECIST 1.1 criteria were used to evaluate the curative effect of overall and different CRP group. The Survival data were followed up and analyzed among different groups. The COX proportional hazard regression model was employed to analyze the independent prognostic factors of first-line chemotherapy for advanced pancreatic cancer. Results All patients were evaluable for efficacy. The disease control rate(DCR) was 50.82% including PR 6 cases, SD 25 cases and PD 4 cases. Until December 31, 2013, 54 cases died and 7 cases survived with medium overall survival(OS) of 7.2 months and medium progressionfree survival(PFS) of 3.03 months. The DCR, medium OS and PFS of A1, A2, B1 and B2 groups were 35.0%, 54.6%, 41.2% and 84.6%, 4.97, 8.87, 7.20 and 10.47 months, and 1.97, 3.83, 3.20, 6.90 months all with significant difference(P<0.05). The independent prognostic factors in patients with advanced pancreatic cancer includes baseline CRP, the dynamic changes of CRP, albumin and CA19-9 levels. Conclusion CRP is one of the biological markers indicating the clinical prognosis of advanced pancreatic cancer. Baseline CRP and CRP kinetics during first-line chemotherapy are independent factors for prognosis of advanced pancreatic cancer.

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