High levels of serum CA15-3 and residual invasive tumor size are associated with poor prognosis for breast cancer patients with non-pathological complete response after neoadjuvant chemotherapy

J Surg Oncol. 2018 Jul;118(1):228-237. doi: 10.1002/jso.25125. Epub 2018 Jun 24.

Abstract

Background and objectives: To identify surrogate markers for prognosis of breast cancer patients with non-pathological complete response (non-pCR) to neoadjuvant chemotherapy (NAC), our investigation focused on the serum levels of carcinoembryonic antigen (CEA) and carbohydrate antigen (CA15-3) as well as clinicopathological factors both before and after NAC.

Methods: A total of 185 breast cancer patients treated with NAC were recruited. Serum carcinoembryonic antigen and CA15-3 were measured at baseline and at completion of NAC.

Results: Among the non-pCR cancers (n = 142), the disease-free survival (DFS) of patients with CA15-3-low at baseline (3-year DFS: 0.908, n = 73) was significantly better than of those with CA15-3-high (3-year DFS: 0.681, n = 69, P = .0134). Multivariable analysis demonstrated that baseline CA15-3 levels (hazard ratio: 3.31, 95% confidence interval: 1.28-10.23; P = .0122) and residual invasive size (hazard ratio: 4.47, 1.26-28.39; P = .0171) were significant independent factors for DFS. The combination of these factors proved to be an accurate predictor for DFS regardless of breast cancer subtypes.

Conclusions: The combination of residual invasive size and serum CA15-3 levels at baseline seems to be a significant and independent surrogate marker of poor outcome for patients with non-pCR. These findings suggest that these markers may be useful for identifying patients with inferior prognosis and candidates for additional adjuvant treatments.

Keywords: CA15-3; breast cancer; carcinoembryonic antigen (CEA); prognosis; residual cancer; tumor marker.

MeSH terms

  • Anthracyclines / administration & dosage
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Breast Neoplasms / blood*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / pathology
  • Breast Neoplasms / surgery
  • Bridged-Ring Compounds / administration & dosage
  • Carcinoembryonic Antigen / blood*
  • Chemotherapy, Adjuvant
  • Disease-Free Survival
  • Female
  • Humans
  • Ki-67 Antigen / biosynthesis
  • Mucin-1 / blood*
  • Neoadjuvant Therapy
  • Preoperative Care / methods
  • Prognosis
  • Taxoids / administration & dosage
  • Trastuzumab / administration & dosage

Substances

  • Anthracyclines
  • Bridged-Ring Compounds
  • Carcinoembryonic Antigen
  • Ki-67 Antigen
  • MUC1 protein, human
  • Mucin-1
  • Taxoids
  • taxane
  • Trastuzumab

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