Impact of the Relative Dose Intensity of Neoadjuvant Chemotherapy With Anthracycline Followed by Taxane on the Survival of Patients With Human Epidermal Growth Factor Receptor 2-negative Breast Cancer: The JONIE1 Study

Anticancer Res. 2021 Feb;41(2):1063-1068. doi: 10.21873/anticanres.14863.

Abstract

Background/aim: We evaluated the impact of the relative dose intensity (RDI) of neoadjuvant chemotherapy (NAC) on the survival of patients with breast cancer (BC).

Patients and methods: This randomized phase II trial included 188 patients with human epidermal growth factor receptor 2 (HER2)-negative BC treated with anthracycline followed by paclitaxel as NAC. We grouped patients using a relative dose intensity (RDI) threshold of 85% and evaluated clinicopathological features and clinical outcomes.

Results: The 5-year overall survival rate was 91.2% and 76.3%, when RDI ≥85% and <85%, respectively (p=0.015). Age, tumor, and node status, and the RDI were significantly different on univariate analysis, but not on multivariate analysis. An exploratory subgroup analysis revealed that a low RDI was associated with low overall survival of patients with obesity, T1/2 disease, and lymph node metastases.

Conclusion: Maintaining the RDI of NAC is crucial for achieving the survival benefit in selected patients with HER2-negative BC.

Keywords: Breast cancer; neoadjuvant chemotherapy; pathological complete response; prognosis; relative dose intensity.

Publication types

  • Clinical Trial, Phase II
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Aged
  • Anthracyclines / administration & dosage*
  • Anthracyclines / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / mortality
  • Drug Administration Schedule
  • Drug Dosage Calculations
  • Female
  • Humans
  • Middle Aged
  • Neoadjuvant Therapy
  • Paclitaxel / administration & dosage*
  • Paclitaxel / therapeutic use
  • Receptor, ErbB-2 / metabolism*
  • Survival Analysis
  • Treatment Outcome

Substances

  • Anthracyclines
  • ERBB2 protein, human
  • Receptor, ErbB-2
  • Paclitaxel