毕晓峰,张 超,李 茉.血清GDF15诊断及筛查结直肠癌的临床价值[J].中国肿瘤,2020,29(12):970-975.
血清GDF15诊断及筛查结直肠癌的临床价值
Serum Growth Differentiation Factor-15 Levels in the Dia-gnosis and Screening of Colorectal Cancer
中文关键词  修订日期:2020-09-17
DOI:10.11735/j.issn.1004-0242.2020.12.A014
中文关键词:  生长分化因子15  结直肠癌  早期诊断  筛查
英文关键词:growth differentiation factor-15  colorectal cancer  early diagnosis  screening
基金项目:
作者单位
毕晓峰 国家癌症中心/国家肿瘤临床医学研究中心/中国医学科学院北京协和医学院肿瘤医院 
张 超 国家癌症中心/国家肿瘤临床医学研究中心/中国医学科学院北京协和医学院肿瘤医院 
李 茉 国家癌症中心/国家肿瘤临床医学研究中心/中国医学科学院北京协和医学院肿瘤医院 
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中文摘要:
      摘 要:[目的] 通过较大样本回顾性研究生长分化因子15 (GDF-15)在结直肠癌中的诊断价值,并探索GDF15及多肿瘤标志物联合应用辅助诊断早期结直肠癌的临床意义。[方法] 应用GDF15定量检测试剂及化学发光免疫分析法,分别检测未接受治疗结直肠癌患者(441例)、治疗后四周结直肠癌患者(179例)和正常健康人群(617名)血清样本中GDF15、CA19-9和CEA水平,探索结直肠癌患者血清GDF15水平与临床分期等临床特征的相关关系,以及GDF15与CA19-9、CEA联用筛查早期结直肠癌的可能性。[结果]结直肠癌患者血清GDF15水平显著高于正常人群(P<0.001),且其血清水平随患者临床分期进展而显著上升(P<0.001),与肿瘤浸润程度(P=0.04)、淋巴结转移与否(P=0.017)、是否存在远端转移(P<0.001)及发病部位(直肠vs结肠,P=0.007)均显著相关。血清GDF15作为肿瘤标志物诊断结直肠癌的灵敏度显著高于CA19-9和CEA(52.4% vs 14.5%,36.3%),尤其在诊断早期结直肠癌患者时,其灵敏度差异更为显著(Ⅰ期43.4% vs 5.7%,7.5%;Ⅱ期55.0% vs 12.9%,35.0%);GDF15与CEA联合应用诊断结直肠癌的灵敏度可达68.3%,其中Ⅰ期结直肠癌灵敏度为49.1%,Ⅱ期结直肠癌灵敏度为70.0%。[结论] GDF15与结直肠癌的临床进展显著相关,是结直肠癌尤其是早期结直肠癌有价值的血清肿瘤标志物,GDF15和CEA联合检测用于结直肠癌早期筛查具有重要的辅助价值。
英文摘要:
      Abstract:[Purpose] To investigate the diagnostic value of serum growth differentiation factor-15(GDF15) level in patients with colorectal cancer(CRC). [Methods] The serum levels of GDF15,CA19-9 and CEA were analyzed by GDF15 quantitative detection reagent and chemiluminescence immunoassay in 441 untreated CRC patients,179 CRC patients 4 weeks after treatment and 617 healthy subjects,respectively. The association of the serum levels of GDF15 with clinical characters were analyzed. Additionally,the clinical value of combining GDF15 with CA19-9 and CEA was explored in screening of colorectal cancer. [Results] The serum levels of GDF15 in patients with CRC were significantly higher than those in healthy control(P<0.001). A stepwise increase of GDF15 levels was noted with the progress of colorectal cancer(P<0.001),and the levels were significantly correlated with the depth of tumor invasion(P=0.04),lymph node metastasis(P=0.017),remote metastasis(P<0.001) and the location of CRC(P=0.007). The sensitivity of GDF15 was superior to CA19-9 and CEA(52.4% vs 14.5%,36.3%). The sensitivities of GDF15 were 43.4% and 55.0% in stage Ⅰ and stage Ⅱ CRC respectively,significantly higher than those of CA19-9(stage Ⅰ,5.7%;stage Ⅱ,12.9%)and CEA(stage Ⅰ,7.5%;stage Ⅱ,35.0%). Furthermore,GDF15 combined with CEA had a sensitivity of 68.3% in the diagnosis of CRC,that was 49.1% for stage Ⅰ CRC and 70.0% for stage Ⅱ CRC.[Conclusion] GDF15 is significantly related to the clinical stages of CRC. The combination of GDF15 with CEA may be more sensitive in diagnosis and screening of early-stage CRC.
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