Efficacy of Palbociclib and Endocrine Treatment in Heavily Pretreated Hormone Receptor-positive/HER2-negative Advanced Breast Cancer: Retrospective Multicenter Trial

Balkan Med J. 2020 Feb 28;37(2):104-107. doi: 10.4274/balkanmedj.galenos.2020.2019.11.143. Epub 2020 Jan 23.

Abstract

Background: The synthesis of CDK4/6 inhibitors with endocrine treatment in two series of treatment has been widely accepted as the standard for patients with estrogen receptor-positive metastatic breast cancer. In spite of this, the activity of CDK4/6 inhibitors in patients with metastatic breast cancer who have progressed despite receiving multiple lines of treatment is not well understood.

Aims: To report the activity and safety of a CDK4/6 inhibitor (palbociclib) in patients in whom at least three lines of treatment for ER+ metastatic breast cancer had failed.

Study design: Multicenter retrospective observational cohort study.

Methods: In this retrospective observational cohort study, we included 43 patients who received palbociclib after at least three lines of systemic treatment for ER+/HER2− metastatic breast cancer.

Results: The median progression-free survival in our population was 7 months (25th-75th percentile, 4-10), and the median overall survival was 11 months (25th-75th percentile, 6-19). Although there were some adverse events, palbociclib was generally well tolerated, so dose reduction was needed for only six patients (14%).

Conclusion: The efficacy of palbociclib among heavily treated hormone receptor-positive/HER2− patients with advanced breast cancer was acceptable in terms of clinical benefit, and it was generally well tolerated among this population.

Keywords: Breast cancer; palbociclib; CDK4/6 inhibitors.

Publication types

  • Multicenter Study
  • Observational Study

MeSH terms

  • Adult
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / genetics*
  • Cohort Studies
  • Female
  • Hormones / standards*
  • Hormones / therapeutic use
  • Humans
  • Middle Aged
  • Piperazines / standards*
  • Piperazines / therapeutic use
  • Pyridines / standards*
  • Pyridines / therapeutic use
  • Receptor, ErbB-2 / metabolism*
  • Retrospective Studies

Substances

  • Hormones
  • Piperazines
  • Pyridines
  • ERBB2 protein, human
  • Receptor, ErbB-2
  • palbociclib