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Use of serial carcinoembryonic antigen and CA 15.3 assays in detecting relapses in breast cancer patients
Authors:Rafael Molina  Gabriel Zanón  Xavier Filella  Ferran Moreno  Judith Jo  Montserrat Daniels  Maria L. Latre  Nuria Giménez  Jaume Pahisa  Martín Velasco  Antonio M. Ballesta
Affiliation:(1) Laboratory of Biochemistry (Unit for Cancer Research), Department of Obstetrics and Gynecology, Hospital Clínico, School of Medicine, Barcelona, Spain;(2) Laboratory of Biochemistry (Unit for Cancer Research), Department of Radiotherapy, Hospital Clínico, School of Medicine, Barcelona, Spain;(3) Laboratory of Biochemistry (Unit for Cancer Research), Coordinación Oncológica, Hospital Clínico, School of Medicine, Barcelona, Spain;(4) Laboratory of Biochemistry (Unit for Cancer Research), Department of Surgery, Hospital Clínico, School of Medicine, Barcelona, Spain;(5) Laboratory of Biochemistry (Unit for Cancer Research), Hospital Clínico Provincial, C/Villaroel 170, 08036 Barcelona, Spain
Abstract:Summary To evaluate the utility of CEA and CA 15.3 for early diagnosis of recurrence, serial serum determinations of both antigens were performed in 1023 patients (follow-up: 1–10 years, mean 6.2 years) with primary breast cancer (CA 15.3 in 533 cases) and no evidence of residual disease (NED) after radical treatment (radical mastectomy or simple mastectomy and radiotherapy). 246 patients developed metastases during follow-up.Results: CEA and CA 15.3 were elevated (> 10 ng/ml or > 60 U/ml, respectively) prior to diagnosis in 40% (98/246) and 41% (37/91) of the patients with recurrence, with a lead time of 4.9 ± 2.2 and 4.2 ± 2.3 months, respectively. When patients with locoregional recurrences were excluded, sensitivity improved to 46% (CEA) and 54% (CA 15.3), and to 64% with both tumor markers (CEA and/or CA 15.3). Higher levels of both CEA and CA 15.3 at diagnosis of recurrence, higher sensitivity in early diagnosis of relapse, and a higher lead time were found in ER+ (CEA) or PgR+ patients (CA 15.3) than in those that were negative for these receptors in the primary tumor (p < 0.001). Specificity of the tumor markers was 99% for both CEA (777 NED patients) and for CA 15.3 (444 NED patients), respectively. In conclusion, CEA and CA 15.3 are useful tools for early diagnosis of metastases, mainly in those patients with ER+ or PR+ tumors.
Keywords:CEA  CA 15.3  tumor-associated antigens  breast cancer  tumor markers  early diagnosis of relapse  metastases
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