Tumor markers in the early detection of tumor recurrence in breast cancer patients: CA 125, CYFRA 21-1, HER2 shed antigen, LDH and CRP in combination with CEA and CA 15-3

التفاصيل البيبلوغرافية
العنوان: Tumor markers in the early detection of tumor recurrence in breast cancer patients: CA 125, CYFRA 21-1, HER2 shed antigen, LDH and CRP in combination with CEA and CA 15-3
المؤلفون: Irene Blankenburg, Volker Heinemann, Petra Stieber, Dorit Di Gioia, Dorothea Nagel
المصدر: Clinica Chimica Acta. 461:1-7
بيانات النشر: Elsevier BV, 2016.
سنة النشر: 2016
مصطلحات موضوعية: Adult, 0301 basic medicine, Oncology, medicine.medical_specialty, Receptor, ErbB-2, Clinical Biochemistry, CA 15-3, Breast Neoplasms, Biochemistry, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Carcinoembryonic antigen, Antigen, Antigens, Neoplasm, Internal medicine, Biomarkers, Tumor, medicine, Humans, CYFRA 21-1, Early Detection of Cancer, Aged, Retrospective Studies, Tumor marker, Keratin-19, L-Lactate Dehydrogenase, biology, business.industry, Mucin-1, Biochemistry (medical), C-reactive protein, General Medicine, Middle Aged, medicine.disease, Metastatic breast cancer, Carcinoembryonic Antigen, C-Reactive Protein, 030104 developmental biology, CA-125 Antigen, 030220 oncology & carcinogenesis, biology.protein, Female, Neoplasm Recurrence, Local, business
الوصف: Background Kinetics of CA 15-3 and CEA have a high specificity in the early detection of metastatic breast cancer (MBC). However, this high specificity is associated with a lack of sensitivity. To decrease the number of false negative patients, the additional diagnostic potential of an extended panel of biomarkers was evaluated. Methods This analysis was performed as part of a large follow-up study (1998–2010) evaluating 813 patients with a median follow-up of 63 months. After primary therapy, all patients underwent tumor marker monitoring for CEA and CA 15-3 at 6-week intervals. A reproducible previously defined increase (≥ 100%) based on the individual baseline value of each patient was considered as a strong indicator of MBC. For the present analysis, we retrospectively evaluated 1011 blood samples from 95 patients. Forty-seven of these had metastatic disease for the first time at the time of this evaluation, while the remaining 48 patients showed no evidence of disease. The sera of these patients were additionally assessed for the following parameters: cancer antigen (CA) 125, cytokeratin-19 soluble fragment (CYFRA 21-1), HER2 shed antigen, lactate-dehydrogenase (LDH) and C-reactive protein (CRP). Results 26 of 47 patients with MBC showed a reproducible tumor marker increase of at least CEA and/or CA 15-3 (55.3%, true-positive). The remaining 21 patients with MBC showed no increase in CEA or CA 15-3 (44.7%, false negative, FN). By combining all markers mentioned above, 41 of 47 patients with MBC showed a reproducible marker increase with a sensitivity of 87.2% and specificity of 100%. Conclusion This retrospective analysis indicates that a panel of biomarkers can increase the sensitivity of the CA 15-3/CEA combination without loss of specificity. The combined use is therefore helpful for early detection of MBC.
تدمد: 0009-8981
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b06fb3147694a04ac256266fd5953accTest
https://doi.org/10.1016/j.cca.2016.07.014Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....b06fb3147694a04ac256266fd5953acc
قاعدة البيانات: OpenAIRE