Practical application of the CA-62 tumor marker in the initial diagnosis of oncological disease of epithelial origin: assistance to the doctor in interpreting the results

Janneta R. Tcherkassova, Sergei A. Tsurkan, Anna I. Prostyakova, Nikolai V. Suganov, Alexander M. Boroda, Albina I. Khamitova, Alexander P. Roytman
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 Materials and methods. The article used the results and conclusions of blind clinical trials conducted to detect early stages of breast cancer (BC), prostate cancer (PC), colorectal cancer (CRC) and non-small cell lung cancer using the CA-62 tumor marker and other tumor markers. Statistical analysis was performed using the MedCalc program (MedCalc Software Ltd, Belgium). Diagnostic efficiency was assessed in terms of sensitivity, specificity, test accuracy, PPV and NPV, ROC analysis. The significance level was taken as p0.001.
 Results. The use of the standard cut-off value of 5000 U/ml of the CA-62 tumor marker makes it possible to achieve 97% sensitivity with 95% specificity in stage I BC. The combination of tumor markers CA-62 and CA 15-3 allows achieving 100% specificity in differentiation of BC and benign breast hyperplasia. The use of the CA-62 marker (6500 U/ml) in the gray zone of PSA 2.510 ng/ml improves the accuracy of detecting PC in biopsy from 35 to 93.1% with 90% sensitivity and 97% specificity. The use of a combination of tumor markers (CA-625000 U/ml, CYFRA 21-12.5 ng/ml and CEA5 ng/ml) will allow the doctor to improve the efficiency of differentiating lung cancer from chronic obstructive pulmonary disease. The combined use of markers (CEA3.5 ng/ml) and (CA-625000 U/ml) achieves 100% specificity with 97% sensitivity in detecting early stages of CRC.
 Conclusion. The article shows the possibilities of using the CA-62 marker, as well as new algorithms for the detection and differentiation of early stages of BC, PC, non-small cell lung cancer and CRC and benign neoplasms using the CA-62 marker in primary diagnosis. The use of the CA-62 tumor marker or its combination with other diagnostic methods can be a useful strategy for a comprehensive assessment of the risk of malignant neoplasms and increasing the diagnostic sensitivity of detecting early stages of cancer.","PeriodicalId":10550,"journal":{"name":"Consilium Medicum","volume":"4 2","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Consilium Medicum","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26442/20751753.2023.6.202307","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Aim. Demonstration the possibility of practical application of the highly sensitive tumor marker CA-62 in the initial diagnosis in asymptomatic patients with suspected cancer and/or the presence of pathological changes in instrumental studies, as well as describe the criteria for interpreting the results to help the doctor make a decision. Materials and methods. The article used the results and conclusions of blind clinical trials conducted to detect early stages of breast cancer (BC), prostate cancer (PC), colorectal cancer (CRC) and non-small cell lung cancer using the CA-62 tumor marker and other tumor markers. Statistical analysis was performed using the MedCalc program (MedCalc Software Ltd, Belgium). Diagnostic efficiency was assessed in terms of sensitivity, specificity, test accuracy, PPV and NPV, ROC analysis. The significance level was taken as p0.001. Results. The use of the standard cut-off value of 5000 U/ml of the CA-62 tumor marker makes it possible to achieve 97% sensitivity with 95% specificity in stage I BC. The combination of tumor markers CA-62 and CA 15-3 allows achieving 100% specificity in differentiation of BC and benign breast hyperplasia. The use of the CA-62 marker (6500 U/ml) in the gray zone of PSA 2.510 ng/ml improves the accuracy of detecting PC in biopsy from 35 to 93.1% with 90% sensitivity and 97% specificity. The use of a combination of tumor markers (CA-625000 U/ml, CYFRA 21-12.5 ng/ml and CEA5 ng/ml) will allow the doctor to improve the efficiency of differentiating lung cancer from chronic obstructive pulmonary disease. The combined use of markers (CEA3.5 ng/ml) and (CA-625000 U/ml) achieves 100% specificity with 97% sensitivity in detecting early stages of CRC. Conclusion. The article shows the possibilities of using the CA-62 marker, as well as new algorithms for the detection and differentiation of early stages of BC, PC, non-small cell lung cancer and CRC and benign neoplasms using the CA-62 marker in primary diagnosis. The use of the CA-62 tumor marker or its combination with other diagnostic methods can be a useful strategy for a comprehensive assessment of the risk of malignant neoplasms and increasing the diagnostic sensitivity of detecting early stages of cancer.
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CA-62肿瘤标志物在上皮源性肿瘤疾病初步诊断中的实际应用:协助医生解释结果
的目标。演示高灵敏度肿瘤标志物CA-62在仪器研究中疑似癌症和/或存在病理变化的无症状患者的初步诊断中实际应用的可能性,并描述解释结果的标准,以帮助医生做出决定。 材料和方法。本文采用CA-62肿瘤标志物及其他肿瘤标志物检测早期乳腺癌(BC)、前列腺癌(PC)、结直肠癌(CRC)和非小细胞肺癌的盲法临床试验结果和结论。使用MedCalc程序(MedCalc Software Ltd, Belgium)进行统计分析。从敏感性、特异性、检测准确性、PPV和NPV、ROC分析等方面评价诊断效率。显著性水平为p0.001。 结果。使用标准临界值5000 U/ml的CA-62肿瘤标志物,可以在I期BC中达到97%的灵敏度和95%的特异性。肿瘤标志物CA-62和CA 15-3的联合使用可以100%特异性地鉴别乳腺癌和乳腺良性增生。在PSA 2.510 ng/ml的灰色区域使用CA-62标记物(6500 U/ml),将活检中PC的检测准确率从35%提高到93.1%,灵敏度为90%,特异性为97%。联合使用肿瘤标志物(CA-625000 U/ml, CYFRA 21-12.5 ng/ml和CEA5 ng/ml)将使医生提高肺癌与慢性阻塞性肺疾病的鉴别效率。联合使用标记物(CEA3.5 ng/ml)和(CA-625000 U/ml)检测早期结直肠癌的特异性为100%,灵敏度为97%。 结论。本文介绍了CA-62标志物在早期诊断中用于BC、PC、非小细胞肺癌、CRC和良性肿瘤的检测和鉴别的可能性,以及CA-62标志物在早期诊断中的新算法。CA-62肿瘤标志物的使用或其与其他诊断方法的结合可作为一种有用的策略,用于全面评估恶性肿瘤的风险,并提高检测早期癌症的诊断敏感性。
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