Clinical Value of Serum p53 Antibody in the Diagnosis and Prognosis of Esophageal Squamous Cell Carcinoma

被引:27
作者
Kunizaki, Masaki [1 ]
Hamasaki, Keiko [1 ]
Wakata, Kouki [1 ]
Tobinaga, Syuichi [1 ]
Sumida, Yorihisa [1 ]
Hidaka, Shigekazu [1 ]
Yasutake, Toru [1 ]
Miyazaki, Takuro [1 ]
Matsumoto, Keitaro [1 ]
Yamasaki, Takuya [2 ]
Sawai, Terumitsu [1 ]
Hamamoto, Ryuji [3 ]
Nanashima, Atsushi [1 ]
Nagayasu, Takeshi [1 ]
机构
[1] Nagasaki Univ Hosp, Dept Surg Oncol, Nagasaki, Japan
[2] Nagasaki Univ Hosp, Dept Radiol, Nagasaki, Japan
[3] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Lab Genome Technol, Tokyo, Japan
基金
日本学术振兴会;
关键词
Esophageal squamous cell carcinoma; tumor marker; serum p53 antibody; COLORECTAL-CANCER; PANCREATIC-CANCER; POOR-PROGNOSIS; IDENTIFICATION; LANDSCAPE; SURVIVAL; TUMORS; SCORE;
D O I
10.21873/anticanres.12419
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Identifying useful biomarkers is central to selecting optimal therapeutic strategies for esophageal squamous cell carcinoma (ESCC). Serum p53 antibody (S-p53Ab), squamous cell carcinoma antigen (SCC-Ag), and carcinoembryonic antigen (CEA) were investigated to evaluate the significance of single and combined tumor markers in determining the diagnosis and prognosis of ESCC. Materials and Methods: Serum samples were obtained preoperatively from 133 patients with histologically-confirmed ESCC, including 32 patients with stage I (24.1%). Levels of S-p53Ab were assessed by enzyme-linked immunosorbent assay, using a new version of a highly specific, quantitative kit. The cut-off value for S-p53Ab was 1.3 U/ml. Results: S-p53Ab was detected in 39.1% (52 out of 133) of patients with ESCC, including 40.0% (20 out of 50) of patients with early-stage ESCC. Positive rates for S-p53Ab, CEA, and SCC-Ag among patients with stage I ESCC (n=32) were 40.6%, 12.5%, and 31.3%, respectively. Positivity for S-p53Ab was not associated with positivity for CEA or SCCAg (p=0.249 and 0.747, respectively). The positive rate for diagnosis of ESCC increased from 39.1% to 65.4% when Sp53Ab was combined with SCC-Ag in this study. We found no significant correlation between the presence of S-p53Ab in ESCC and overall survival. Conversely, Cox regression analysis revealed that the International Union Against Cancer/TNM classification and systemic inflammation score were independent prognostic factors for ESCC in this series (hazard ratio(HR)=3.811, 95% confidence interval(CI)=1.548-9.378, p=0.004; and HR=2.218; 95% CI=1.087-4.523, p=0.029, respectively). Kaplan-Meier analysis revealed significant differences between patients with elevated S-p53Ab and SCC-Ag and patients with elevated levels of only one or neither of these factors (p=0.009). Conclusion: The diagnostic rate with S-p53Ab was better than that with SCC-Ag and CEA in patients with early-stage ESCC. Combined detection of S-p53Ab and SCC-Ag can markedly improve diagnostic sensitivity and may permit more accurate stratification of patients with ESCC.
引用
收藏
页码:1807 / 1813
页数:7
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