Oncologic necessity for the complete removal of residual microcalcifications after neoadjuvant chemotherapy for breast cancer

Sci Rep. 2022 Dec 13;12(1):21535. doi: 10.1038/s41598-022-24757-7.

Abstract

The surgical range of breast cancer that shows pathologic complete response (pCR) without change in microcalcifications after neoadjuvant chemotherapy (NAC) is controversial. This study examined whole breast specimens to evaluate the necessity of mastectomy in those cases. The viability of cancer cells around the residual microcalcification was assessed using prospectively collected breast samples to confirm the presence or absence of cancer cells. A total of 144 patients with breast cancer and diffuse microcalcifications were classified into the reduced mass with no change in residual microcalcification (RESMIN, n = 49) and non-RESMIN (n = 95) groups. Five specimens were prospectively evaluated to assess the presence of viable cancer cells around the microcalcification. Tumor responses to NAC were significantly better with high pCR rates in the RESMIN group (p = 0.005 and p = 0.002). The incidence of human epidermal growth factor receptor 2-positive and triple-negative breast cancers was significantly high in the RESMIN group (p = 0.007). Although five (10.2%) patients had locoregional recurrence in the RESMIN group, no local recurrence in the breast was reported. Although pCR was highly estimated, residual cancers, including ductal carcinoma in situ, remained in 80% cases. Therefore, given the weak scientific evidence available currently, complete removal of residual microcalcifications should be considered for oncologic safety.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Breast Neoplasms* / pathology
  • Calcinosis* / pathology
  • Chemotherapy, Adjuvant
  • Female
  • Humans
  • Mammography
  • Mastectomy
  • Neoadjuvant Therapy
  • Neoplasm Recurrence, Local / drug therapy
  • Receptor, ErbB-2 / metabolism
  • Retrospective Studies
  • Triple Negative Breast Neoplasms* / pathology

Substances

  • Receptor, ErbB-2