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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.
Abstract:
Tumors affect the immune system, locally and systemically. The frequencies of specific circulating immune cell populations correlate with disease progression as well as prognosis of the patients. Although largely neglected, conventional antitumoral therapies often possess immunomodulatory properties and affect the levels of specific immune cell populations. Most information, however, derive from animal or in vitro studies. As this could impact prognosis as well as response to therapy, further studies of the effects of treatment on circulating immune cells in patients are warranted. In this pilot study, we evaluated a wide panel of circulating immune cells over time (up to six months) in ten patients with metastatic breast cancer receiving standard antitumoral regimens. Overall, endocrine therapy tends to enrich for natural killer (NK) and natural killer T (NKT) cells in the circulation, whereas both chemotherapy and endocrine therapy reduce the levels of circulating monocytic myeloid-derived suppressor cells (Mo-MDSCs). This indicates that the systemic immunosuppressive profile observed in patients tends to revert over the course of systemic therapy and holds promise for future combination treatment with standard antitumoral agents and immunotherapy.
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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