Treatment with Granulocyte-colony Stimulating Factor (G-CSF) is not associated with Increased Risk of Brain Metastasis in Patients with De Novo Stage IV Breast Cancer

Background: Survival outcome after developing brain metastasis is poor and there is an unmet need to identify factors that can promote brain metastasis. Granulocyte-colony stimulating factor (G-CSF) is given to support neutrophil recovery after myelosuppressive chemotherapy to some patients. However, there is emerging evidence that neutrophils can promote metastasis, including through the formation of neutrophil extracellular traps (NETs), scaffolds of chromatin with enzymes expelled from neutrophils to the extracellular space. In animal models, G-CSFs can induce NETs to promote liver and lung metastasis. The primary objective of this study was to test the association between G-CSF use and the later incidence of brain metastasis. Methods: Patients with de novo Stage IV breast cancer, without known brain metastasis at the time of initial diagnosis, were identified from electronic medical records covering the period from 1/1/2013 to 12/31/2020 at Northwell Health. Univariate and multivariate logistic regression models were used to test the association between variables of interest, including G-CSF use, and brain metastasis. Results: A total of 78 patients were included in the final analysis. Among those 78 patients, 24 patients (30.8%) had received G-CSF along with chemotherapy at least once. In logistic regression models, G-CSF use was not a significant factor to predict brain metastasis (OR 1.89 [95%CI 1.89-5.33]; P=0.23). Interestingly, in multivariate logistic models, pulmonary embolism (PE)/deep venous thrombosis (DVT) was a significant predictive factor of brain metastasis (OR 6.74 [95%CI 1.82-25.01]; P=0.004) (38.5% vs 21.5%). Conclusions: The use of G-CSF was not associated with increased risk of brain metastasis in patients with de novo Stage IV breast cancer. Interestingly, PE/DVT, which can be associated with elevated NETs, was associated with brain metastasis. Further studies are warranted to determine whether DVT/PE with or without elevated NETs levels in the blood, is predictive of developing brain metastasis in patients with de novo Stage IV breast cancer.

[1]  N. Mackman,et al.  Prognostic value of circulating markers of neutrophil activation, neutrophil extracellular traps, coagulation and fibrinolysis in patients with terminal cancer , 2021, Scientific Reports.

[2]  A. Jemal,et al.  Cancer Statistics, 2021 , 2021, CA: a cancer journal for clinicians.

[3]  E. Song,et al.  DNA of neutrophil extracellular traps promotes cancer metastasis via CCDC25 , 2020, Nature.

[4]  Jun Yao,et al.  Blocking immunosuppressive neutrophils deters pY696-EZH2–driven brain metastases , 2020, Science Translational Medicine.

[5]  Xiaohua Yan,et al.  The role of granulocyte colony-stimulating factor in breast cancer development: A review , 2020, Molecular medicine reports.

[6]  B. Boone,et al.  Neutrophil extracellular traps in breast cancer and beyond: current perspectives on NET stimuli, thrombosis and metastasis, and clinical utility for diagnosis and treatment , 2019, Breast Cancer Research.

[7]  E. Lengyel,et al.  Neutrophils facilitate ovarian cancer premetastatic niche formation in the omentum , 2019, The Journal of experimental medicine.

[8]  Michael S. Goldberg,et al.  Neutrophil extracellular traps produced during inflammation awaken dormant cancer cells in mice , 2018, Science.

[9]  D. Wagner,et al.  Citrullinated histone H3, a biomarker of neutrophil extracellular trap formation, predicts the risk of venous thromboembolism in cancer patients , 2018, Journal of thrombosis and haemostasis : JTH.

[10]  J. Hamilton,et al.  Neutrophils, G‐CSF and their contribution to breast cancer metastasis , 2018, The FEBS journal.

[11]  L. Desender,et al.  Neutrophil extracellular traps in ischemic stroke thrombi , 2017, Annals of neurology.

[12]  N. C. Rochael,et al.  Tumor-Derived Exosomes Induce the Formation of Neutrophil Extracellular Traps: Implications For The Establishment of Cancer-Associated Thrombosis , 2017, Scientific Reports.

[13]  Michael S. Goldberg,et al.  Cancer cells induce metastasis-supporting neutrophil extracellular DNA traps , 2016, Science Translational Medicine.

[14]  D. Edwards,et al.  Erratum: Oncogenic mTOR signalling recruits myeloid-derived suppressor cells to promote tumour initiation , 2016, Nature Cell Biology.

[15]  S. Jalkanen,et al.  G-CSF regulates macrophage phenotype and associates with poor overall survival in human triple-negative breast cancer , 2015, Oncoimmunology.

[16]  Thomas J. Smith,et al.  Recommendations for the Use of WBC Growth Factors: American Society of Clinical Oncology Clinical Practice Guideline Update. , 2015, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[17]  John M S Bartlett,et al.  Recommendations for human epidermal growth factor receptor 2 testing in breast cancer: American Society of Clinical Oncology/College of American Pathologists clinical practice guideline update. , 2014, Archives of pathology & laboratory medicine.

[18]  Paul Kubes,et al.  Neutrophil extracellular traps sequester circulating tumor cells and promote metastasis. , 2013, The Journal of clinical investigation.

[19]  V. Papayannopoulos,et al.  Molecular mechanisms regulating NETosis in infection and disease , 2013, Seminars in Immunopathology.

[20]  D. Scadden,et al.  Cancers predispose neutrophils to release extracellular DNA traps that contribute to cancer-associated thrombosis , 2012, Proceedings of the National Academy of Sciences.

[21]  I. Fidler The role of the organ microenvironment in brain metastasis. , 2011, Seminars in cancer biology.

[22]  J. Hartwig,et al.  Extracellular DNA traps promote thrombosis , 2010, Proceedings of the National Academy of Sciences.

[23]  G. Lyman,et al.  Colony-stimulating factors for chemotherapy-induced febrile neutropenia: a meta-analysis of randomized controlled trials. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[24]  B. Wiens,et al.  First and subsequent cycle use of pegfilgrastim prevents febrile neutropenia in patients with breast cancer: a multicenter, double-blind, placebo-controlled phase III study. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[25]  E. Winer,et al.  CNS metastases in breast cancer. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[26]  A. Zychlinsky,et al.  Neutrophil Extracellular Traps Kill Bacteria , 2004, Science.

[27]  I. Fidler,et al.  The biology of brain metastasis. , 2013, Clinical chemistry.

[28]  D. Brizel,et al.  National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines in Oncology , 2012 .

[29]  N. Dubrawsky Cancer statistics , 1989, CA: a cancer journal for clinicians.