Identification of high-risk patients by human epididymis protein 4 levels during follow-up of ovarian cancer

被引:28
作者
Steffensen, Karina Dahl [1 ,2 ]
Waldstrom, Marianne [3 ]
Brandslund, Ivan [4 ]
Lund, Bente [5 ]
Sorensen, Sarah Mejer [6 ]
Petzold, Max [7 ]
Jakobsen, Anders [1 ,2 ]
机构
[1] Vejle Hosp, Dept Oncol, Kabbeltoft 25, DK-7100 Vejle, Denmark
[2] Univ Southern Denmark, Inst Reg Hlth Res, DK-5000 Odense, Denmark
[3] Vejle Hosp, Dept Pathol, DK-7100 Vejle, Denmark
[4] Vejle Hosp, Dept Clin Biochem, DK-7100 Vejle, Denmark
[5] Aalborg Univ Hosp, Dept Oncol, DK-9100 Aalborg, Denmark
[6] Univ Copenhagen, Fac Hlth Sci, DK-2200 Copenhagen, Denmark
[7] Univ Gothenburg, Sahlgrenska Acad, Ctr Appl Biostat, S-40530 Gothenburg, Sweden
关键词
ovarian cancer; human epididymis protein 4; carbohydrate antigen 125; follow-up; recurrence; biomarker; HE-4; CA-125; CARCINOMA; BIOMARKER; CA125; PROGRESSION; GUIDELINES; EXPRESSION; MULTIPLE; EVALUATE;
D O I
10.3892/ol.2016.4533
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The majority of ovarian cancer patients with advanced disease at diagnosis will relapse following primary treatment, with a dismal prognosis. Monitoring the levels of serum markers in patients under follow-up may be essential for the early detection of relapse, and for distinguishing high-risk patients from those with less aggressive disease. The aim of the present study was to investigate the possible predictive value of human epididymis protein 4 (HE4) and carbohydrate antigen 125 (CA125) in relation to recurrence of epithelial ovarian cancer by measuring the two markers during follow-up subsequent to surgery and adjuvant first-line carboplatin/paclitaxel chemotherapy. Serum HE4 and CA125 were analyzed in 88 epithelial ovarian cancer patients at the end of treatment and consecutively during follow-up. The patients were divided into a high-risk and a low-risk group based on having an increase in HE4 and CA125 levels above or below 50% during follow-up, relative to the baseline (end-of-treatment) level. Disease recurrence was detected in 55 patients during follow-up. Patients with an increase in HE4 of >50% at 3- and 6-month follow-up compared to the end-of-treatment sample had significantly poorer progression-free survival (PFS) [hazard ratio (HR), 2.82 (95% CI, 0.91-8.79; P=0.0052) and HR, 7.71 (95% CI, 3.03-19.58; P<0.0001), respectively]. The corresponding 3- and 6-month biomarker assessments for increased CA125 levels (>50%) showed HRs of 1.86 (95% CI, 0.90-3.80; P=0.0512) and 2.55 (95% CI, 1.39-4.68; P=0.0011), respectively. Multivariate analysis confirmed HE4 as a predictor of short PFS, with an HR of 8.23 (95% CI, 3.28-20.9; P<0.0001) at 6-month follow-up. The increase of CA125 was not a significant prognostic factor in multivariate analysis for PFS. In conclusion, HE4 appears to be a sensitive marker of recurrence and instrumental in risk assessment during the first 6 months of follow-up.
引用
收藏
页码:3967 / 3974
页数:8
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