Impact of grade, hormone receptor, and HER-2 status in women with breast cancer on response to specific chemotherapeutic agents by in vitro adenosine triphosphate-based chemotherapy response assay

J Korean Med Sci. 2009 Dec;24(6):1150-7. doi: 10.3346/jkms.2009.24.6.1150. Epub 2009 Nov 9.

Abstract

This study was designed to assess whether histological and biological factors of breast cancer can predict chemoresponse to specific agents. Adenosine triphosphate-based chemotherapy response assay (ATP-CRA) was employed to retrieve chemoresponse to 5-fluorouracil (5-FU), doxetaxel, doxorubicin, epirubicin, and paclitaxel in 49 patients. Tumors with high histologic and nuclear grade have higher response rate to doxorubicin (P<0.05) and palitaxel (P<0.05). Estrogen receptor (ER)-negative tumors respond well to doxorubicin (P=0.038), and progesterone receptor (PR)-negative tumors to 5-FU (P=0.039), doxetaxel (P=0.038), doxorubicin (P=0.000), epirubicin (P=0.010), and paclitaxel (P=0.003). Among the breast cancer subtypes determined by ER, PR, and HER-2 immunohistochemical stains, the HER-2+/ER- subtype has a higher response rate to doxorubicin (P=0.008). This in vitro result suggests that the combination of histologic and nuclear grade, hormone receptor, and HER-2 status can be a predictive factor of response to specific chemotherapy agents. Further in vivo study should be followed for clinical trials.

Keywords: Breast Neoplasms; Drug Therapy; Tumor Markers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Adult
  • Aged
  • Antineoplastic Agents / therapeutic use*
  • Breast Neoplasms* / classification
  • Breast Neoplasms* / drug therapy
  • Breast Neoplasms* / pathology
  • Doxorubicin / therapeutic use
  • Drug Screening Assays, Antitumor / methods*
  • Epirubicin / therapeutic use
  • Female
  • Fluorouracil / therapeutic use
  • Humans
  • Middle Aged
  • Paclitaxel / therapeutic use
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / metabolism*
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism
  • Receptors, Progesterone / genetics
  • Receptors, Progesterone / metabolism

Substances

  • Antineoplastic Agents
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Epirubicin
  • Doxorubicin
  • Adenosine Triphosphate
  • ERBB2 protein, human
  • Receptor, ErbB-2
  • Paclitaxel
  • Fluorouracil