Nanoparticle albumin-bound paclitaxel-based neoadjuvant regimen: A promising treatment option for HER2-low-positive breast cancer

Nanomedicine. 2023 Apr:49:102666. doi: 10.1016/j.nano.2023.102666. Epub 2023 Mar 6.

Abstract

This study aimed to compare the efficacy of neoadjuvant systemic therapy (NST) with solvent-based paclitaxel (Sb-P), liposomal paclitaxel (Lps-P), nanoparticle albumin-bound paclitaxel (Nab-P), and docetaxel in human epidermal growth factor receptor 2 (HER2)-low-positive and HER2-zero breast cancers. A total of 430 patients receiving 2-weekly dose-dense epirubicin and cyclophosphamide (EC) followed by 2-weekly paclitaxel (Sb-P, Lps-P, or Nab-P), or 3-weekly EC followed by 3-weekly docetaxel for NST were enrolled in the study. In HER2-low-positive patients, the pathological complete response (pCR) rate in Nab-P group was significantly higher than that in the other three paclitaxel groups (2.8 % in Sb-P group, 4.7 % in Lps-P group, 23.2 % in Nab-P group and 3.2 % in docetaxel group, p < 0.001). In HER2-zero patients, the pCR rate did not differ significantly among the four paclitaxel groups (p = 0.278). The NST regimen containing Nab-P could be considered a promising treatment option in HER2-low-positive breast cancer.

Keywords: HER2-low-positive breast cancer; Nanoparticle albumin-bound paclitaxel; Neoadjuvant systemic therapy; Paclitaxel; Pathological complete response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albumin-Bound Paclitaxel / therapeutic use
  • Albumins
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Breast Neoplasms* / pathology
  • Cyclophosphamide / therapeutic use
  • Docetaxel / therapeutic use
  • Epirubicin / therapeutic use
  • Female
  • Humans
  • Lipopolysaccharides
  • Nanoparticles*
  • Neoadjuvant Therapy
  • Paclitaxel / therapeutic use
  • Receptor, ErbB-2 / metabolism
  • Treatment Outcome

Substances

  • Albumin-Bound Paclitaxel
  • Docetaxel
  • Lipopolysaccharides
  • Cyclophosphamide
  • Epirubicin
  • Paclitaxel
  • Albumins
  • Receptor, ErbB-2