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. 2014 Mar 16;5(4):281–290. doi: 10.7150/jca.8016

Table 1.

Summaries from Recent Studies Using Serum Tumor Markers to Monitor for Recurrence in the Adjuvant Setting

Reference Patients Intervention Outcome
Zervoudis (2007)40 358 patients with stage I breast cancer who were disease free after primary treatment. Clinical exam, mammography, bone scintigraphy, annual CT of the chest and abdomen and multiple serum tumor markers including CEA, CA 15-3, CA 27-29 every 4 months 18 patients (5%) had increased tumor markers by cutoff values. All of them had negative workup for disease.
After 5 years of follow up, 15 of those 18 patients remained free of local recurrence or metastatic disease and the other 3 were lost to follow up.
Nicolini (2006)41 268 breast cancer patients that were disease free at the start of the study. All stages seem to have been represented and were treated according to guidelines. Serial serum CEA, CA 15-3, TPA, MCA were measured every 4-6 months.
Bone scan, liver ultrasound, and chest x ray were performed every 24-36 months to detect any false negatives.
There were 19 relapses. Mean lead times between tumor marker elevation and the appearance of disease were between about 3-7 months depending on the tumor marker
Sensitivities ranged from 10-68%.
222 patients were found to have tumor marker elevations for non-malignant reasons leading to specificities around 40-70%
Valenzuela (2002)42 318 patients who were disease-free after primary therapy CA 15.3 and CEA were measured in serum at each routine follow up visit 59 patients relapsed, 28 of whom had elevated CA 15-3 levels and 31 of whom did not.
30 patients had false positive elevations of CA 15-3.
17 patients had elevated tumor markers (16 CA 15-3 and 1 CEA) before clinical appearance of metastases.
Pedersen (2013)43 9 patients with local recurrence and 83 patients who developed distant metastases after primary treatment. Patients who originally presented with distant metastases were excluded. CA 15-3, CEA, and HER2 were measured. A result was considered positive if above a certain threshold. None of the patients with local recurrence had elevated serum tumor markers.
The most sensitive marker to detect recurrence was CA 15-3 (49.4%).
The most sensitive combination was CA 15-3 and CEA (60.2%)
In patients with HER2+ tumors, the sensitivity of serum HER2 was 55.6% and 21.2% in patients with HER2 negative tumors

CEA = carcinoembryonic antigen, MCA = mucin-like carcinoma associated antigen, TPA = tissue polypeptide. Of note, each study used different cutoff values for identifying a patient as positive, though all followed trends in this marker.