Clinical utility of tumour marker velocity of cancer antigen 15–3 (CA 15–3) and carcinoembryonic antigen (CEA) in breast cancer surveillance

癌胚抗原 医学 乳腺癌 内科学 尤登J统计 预测标记 肿瘤标志物 约15-3 癌症 CA19-9号 癌抗原 肿瘤科 逻辑回归 代理终结点 胃肠病学 结直肠癌 抗原 病理 预测值 免疫学 CA15-3号 胰腺癌
作者
J.X. Hing,Chi Wei Mok,Pei Ting Tan,S Sudhakar,C.M.J. Seah,W.P. Lee,Su-Ming Tan
出处
期刊:The Breast [Elsevier BV]
卷期号:52: 95-101 被引量:48
标识
DOI:10.1016/j.breast.2020.05.005
摘要

Abstract

Background

Serum tumour markers, cancer antigen 15–3 (CA 15–3) and carcinoembryonic antigen (CEA) are not routinely recommended for detecting breast cancer recurrence and monitoring treatment. In this study, we aim to evaluate the diagnostic accuracy of absolute CA 15–3 and CEA levels and report on the clinical utility of tumour marker velocity in breast cancer surveillance.

Methods

67 consecutive patients over a 15-year period (1998–2012) with available serial serum CA 15–3 and CEA measurements at recurrence were matched to a control group of patients. Tumour marker velocity was derived from the average change in consecutive tumour marker values over time, expressed in unit/year. Logistic regression analysis was performed to investigate the association between tumour characteristics, tumour marker velocity and disease recurrence.

Results

Using the Youden index values, the optimal cut-off values for absolute CA 15–3 and CEA corresponded to the normal assay reference range while tumour marker velocity values were derived to be 2.5U/mL/year and 1.2ng/mL/year respectively. CA 15–3 velocity > 2.5U/mL/year had the highest AUROC value of 0.85 than CEA velocity alone. When either tumour marker velocity exceeded threshold values, the sensitivity, specificity, negative predictive value and positive predictive value were 94.0%, 73.1%, 92.5%, and 77.8% respectively. In the multivariate logistic regression analysis, having both CA 15–3 and CEA velocity exceeding the cut-off values was shown to be a significant predictor for disease recurrence (p = 0.01).

Conclusion

These findings highlighted the clinical utility of serial tumour markers measurements and its velocity in breast cancer surveillance.

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