Impact of systemic therapy on circulating leukocyte populations in patients with metastatic breast cancer

Anna-Maria Larsson1,2, Anna Roxå1, Karin Leandersson3

  • 1Department of Clinical Sciences Lund, Division of Oncology and Pathology, Lund University, Lund, Sweden.

Scientific Reports
|September 19, 2019
PubMed

Insights

Standard cancer therapies can alter immune cell levels in patients. This pilot study in metastatic breast cancer found endocrine therapy increased natural killer (NK) and natural killer T (NKT) cells, while chemotherapy and endocrine therapy decreased monocytic myeloid-derived suppressor cells (Mo-MDSCs).

Area of Science:

  • Immunology
  • Oncology
  • Pharmacology

Background:

  • Tumors significantly impact the immune system, influencing patient prognosis and disease progression.
  • Conventional antitumoral therapies possess immunomodulatory effects, altering circulating immune cell populations.
  • Existing data on treatment effects on immune cells primarily come from animal or in vitro studies, necessitating patient-based research.

Purpose of the Study:

  • To investigate the dynamic changes in circulating immune cell populations in patients with metastatic breast cancer undergoing standard antitumoral therapies.
  • To assess the impact of endocrine therapy and chemotherapy on specific immune cell subsets over time.
  • To explore the potential for reversing systemic immunosuppression through standard treatments.

Main Methods:

  • A pilot study involving ten patients with metastatic breast cancer.
  • Longitudinal evaluation of a wide panel of circulating immune cells for up to six months.
  • Analysis of immune cell population shifts in response to standard antitumoral regimens (endocrine therapy and chemotherapy).

Main Results:

  • Endocrine therapy was associated with an enrichment of natural killer (NK) and natural killer T (NKT) cells in circulation.
  • Both chemotherapy and endocrine therapy led to a reduction in circulating monocytic myeloid-derived suppressor cells (Mo-MDSCs).
  • Systemic immunosuppressive profiles showed a tendency to revert during the course of therapy.

Conclusions:

  • Standard antitumoral therapies, including endocrine therapy and chemotherapy, modulate circulating immune cell populations in metastatic breast cancer patients.
  • Therapy-induced changes suggest a potential reversal of systemic immunosuppression.
  • These findings support future investigations into combination treatments involving standard therapies and immunotherapy.

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