Apoptosis induced by neoadjuvant chemotherapy in breast cancer

Pathology. 2006 Feb;38(1):21-7. doi: 10.1080/00313020500465315.

Abstract

Aim: To evaluate the relationship between apoptosis induced by chemotherapy and clinical response in breast cancer.

Methods: Apoptosis index (AI), mutant p53 and Bcl-2 protein expression were evaluated in 44 breast tumour samples from patients submitted to neoadjuvant chemotherapy. Objective response (OR) to primary chemotherapy was observed in 37 patients (84%) and no response (NR) in seven. AI was measured by the rate of apoptotic cells identified using morphological criteria. p53 and Bcl-2 protein expression were evaluated using an immunoperoxidase staining technique.

Results: The median AI change observed between pre-chemotherapy AI and post-chemotherapy AI was 0.84 in the OR group and 0.01 in the NR group, (rho = 0.4; p = 0.006). There was no change in Bcl-2 protein expression following chemotherapy. In the OR group, p53 protein expression was positive in 41.6% of patients before and in 22.2% after chemotherapy (difference = 16.6%; p = 0.03). No change was detected in the NR group.

Conclusion: A positive correlation was found between the increase in AI and clinical response to neoadjuvant chemotherapy in locally advanced breast cancer.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anthracyclines / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Apoptosis* / drug effects
  • Apoptosis* / genetics
  • Breast Neoplasms / chemistry
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / pathology*
  • Bridged-Ring Compounds / therapeutic use
  • Chemotherapy, Adjuvant
  • Cyclophosphamide / therapeutic use
  • Drug Resistance, Neoplasm
  • Epirubicin / therapeutic use
  • Female
  • Fluorouracil / therapeutic use
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunohistochemistry
  • Middle Aged
  • Mutation
  • Neoadjuvant Therapy
  • Proto-Oncogene Proteins c-bcl-2 / analysis
  • Taxoids / therapeutic use
  • Tumor Suppressor Protein p53 / analysis

Substances

  • Anthracyclines
  • Bridged-Ring Compounds
  • Proto-Oncogene Proteins c-bcl-2
  • Taxoids
  • Tumor Suppressor Protein p53
  • taxane
  • Epirubicin
  • Cyclophosphamide
  • Fluorouracil

Supplementary concepts

  • FEC protocol