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人附睾蛋白4在卵巢癌诊断及预后评估中价值 被引量:1

Value of human epididymal protein 4 to the diagnosis and prognosis assessment of ovarian cancer
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摘要 目的观察卵巢癌患者尿液及血清人附睾蛋白4(human epididymis protein 4,HE4)水平,探讨其在临床诊断及预后评估中的价值。方法卵巢癌患者33例为卵巢癌组,其中FIGO分期Ⅰ期10例,Ⅱ期5例,Ⅲ期11例,Ⅳ期7例,均行全面分期术/减瘤术;卵巢良性疾病患者33例为卵巢良性病变组,同期体检健康者33例为对照组。3组均检测尿液及血清HE4水平,比较3组及不同FIGO分期卵巢癌患者尿液及血清HE4水平。随访观察卵巢癌患者生存情况,采用多因素Cox比例风险回归模型分析卵巢癌患者术后疾病进展及发生全因死亡的危险因素。结果卵巢癌组尿液、血清HE4水平[(11.84±4.52)、(150.67±21.47)pmol/L]均高于卵巢良性病变组[(3.31±1.35)、(45.52±12.62)pmol/L]和对照组[(3.26±1.15)、(35.31±9.41)pmol/L](P<0.05);FIGO分期Ⅲ、Ⅳ期患者尿液HE4[(19.67±5.21)、(21.34±5.23)pmol/L]及血清HE4[(170.23±25.28)、(180.74±26.34)pmol/L]水平均高于Ⅰ期[(10.52±3.21)、(107.33±17.83)pmol/L]、Ⅱ期患者[(12.27±3.26)、(118.15±20.21)pmol/L](P<0.05),Ⅰ期与Ⅱ期、Ⅲ与Ⅳ期患者尿液及血清HE4水平比较差异均无统计学意义(P>0.05)。随访36个月,33例卵巢癌患者中病情进展死亡24例,总生存期为(10.2±2.1)个月。FIGO分期Ⅲ/Ⅳ期及尿液HE4≥6.32 pmol/L是卵巢癌患者术后疾病进展和死亡的危险因素(HR=3.50,95%CI:1.720~6.275,P=0.024;HR=5.65,95%CI:1.840~13.260,P=0.013)。结论卵巢癌患者尿液及血清HE4水平均明显升高,FIGO高分期和尿液高HE4水平是卵巢癌患者术后疾病进展和死亡的危险因素。 Objective To observe the levels of urine and serum human epididymal protein 4(HE4)and to investigate their values to the diagnosis and prognosis assessment of ovarian cancer.Methods Thirty-three patients with ovarian cancer(ovarian cancer group)were performed comprehensive staging surgery or debulking surgery,including 10 patients in FIGO stageⅠ,5 in stageⅡ,11 in stageⅢand 7 in stageⅣ,another 33 patients with benign ovarian diseases were selected as benign ovarian diseases group,and 33 healthy volunteers were as controls(control group).The urine and serum HE4 levels were detected and compared in three groups and among patients in different FIGO stages.The survival time was observed in ovarian cancer group.Multivariate Cox’s proportional hazards regression model was used to analyze the risk factors of disease progression and all-cause death after operation in ovarian cancer patients.Results The levels of urine and serum HE4 were higher in ovarian cancer group((11.84±4.52),(150.67±21.47)pmol/L)than those in benign ovarian diseases group((3.31±1.35),(45.52±12.62)pmol/L)and control group((3.26±1.15),(35.31±9.41)pmol/L)(P<0.05),were higher in patients in FIGO stageⅢ((19.67±5.21),(170.23±25.28)pmol/L)and stageⅣ((21.34±5.23),(180.74±26.34)pmol/L)than those in patients in stageⅠ((10.52±3.21),(107.33±17.83)pmol/L)and stageⅡ((12.27±3.26),(118.15±20.21)pmol/L)(P<0.05),and showed no significant differences between patients in stageⅠand stageⅡas well as between patients in stageⅢand stageⅣ(P>0.05).The 36-month follow-up showed that 24 of 33 patients died of disease progression.The overall survival time was(10.2±2.1)months.FIGO stageⅢ/Ⅳand urine HE4≥6.32 pmol/L were the risk factors of disease progression and death in patients with ovarian cancer(HR=3.50,95%CI:1.720-6.275,P=0.024;HR=5.65,95%CI:1.840-13.260,P=0.013).Conclusion The levels of urine and serum HE4 increase obviously in patients with ovarian cancer.High FIGO stage and high level of urine HE4 are the risk factors of disease progression and death.
作者 杨静 董学彩 张梦捷 王爱红 海静 YANG Jing;DONG Xue-cai;ZHANG Meng-jie;WANG Ai-hong;HAI Jing(Department of Gynecology,Xinxiang Central Hospital,the Fourth Clinical College of Xinxiang Medical University,Xinxiang,Henan 453000,China;Department of Obstetrics and Gynecology,the First Affiliated Hospital of Henan University of Science and Technology,Luoyang,Henan 471000,China)
出处 《中华实用诊断与治疗杂志》 2021年第8期819-821,共3页 Journal of Chinese Practical Diagnosis and Therapy
基金 2018年度河南省医学科技攻关计划项目(2018020276)。
关键词 卵巢癌 人附睾蛋白4 预后 ovarian cancer human epididymal protein 4 prognosis
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  • 1Ya-Fei Zhu,Guo-Lan Gao,Sheng-Bo Tang,Zhen-Dong Zhang,Qing-Shui Huang.Effect of WFDC 2 silencing on the proliferation,motility and invasion of human serous ovarian cancer cells in vitro[J].Asian Pacific Journal of Tropical Medicine,2013,6(4):265-272. 被引量:12
  • 2Joshua G Cohen,Matthew White,Ana Cruz,Robin Farias-Eisner.WJBC 5^(th) Anniversary Special Issues(2): Proteomics In 2014, can we do better than CA125 in the early detection of ovarian cancer?[J].World Journal of Biological Chemistry,2014,5(3):286-300. 被引量:18
  • 3Wu R, Baker S J, Hu T C, et al. Type I to type II ovarian carcinoma progression: mutant Trp53 or Pik3ca confers a more aggressive tumor phenotype in a raouse model of ovarian cancer [J]. The American journal of pathology, 2013, 182(4): 1391-1399.
  • 4Bojesen S E, Pooley K A, Johnatty S E, et al. Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer [J]. Nature genetics, 2013, 45 (4): 371-384.
  • 5Pharoah P D P, Tsai Y Y, Ramus S J, et al. GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer [J]. Nature genetics, 2013, 45(4): 362-370.
  • 6Pearce C L, Templeman C, Rossing M A, et al. Association between endometriosis and risk of histological subtypes of ovarian cancer: a pooled analysis of case-control studies[J]. The lancet oncology, 2012, 13(4): 385-394.
  • 7Kaye S B, Lubinski J, Matulonis U, et al. Phase II, open-label, random- ized, multicenter study comparing the efficacy and safety of olaparib, a poly (ADP-ribose) polymerase inhibitor, and pegylated liposoraal doxombicin in patients with BRCA1 or BRCA2 mutations and recur-rent ovarian cancer [J]. Journal of Clinical Oncology, 2012, 30(4): 372-379.
  • 8Kuchenbaecker K B, Ramus S J, Tyrer J, et al. Identification of six new susceptibility loci for invasive epithelial ovarian cancer [J]. Na- ture genetics, 2015, 47(2): 164-171.
  • 9Hellstrom I, Hellstrom K E. fTwo novel biomarkers, mesothelin and HE4, for diagnosis of ovarian carcinoma [J]. Expert Opinion on Med- ical Diagnostics, 2011, 5(3): 227-240.
  • 10Sarikapan W, Chan K K L, Chi An C, et al. Distinguishing benign from malignant pelvic mass utilizing an algorithm with HE4, menopausal status, and ultrasound findings[J]. Journal of Gynecologic Oncology, 2015, 26(1): 46-53.

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