Metastasis: A Bane of Breast Cancer Therapy - European Medical Journal


Metastasis: A Bane of Breast Cancer Therapy

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EMJ 5.3 2020
Chidalu A. Edechi,1 Nnamdi M. Ikeogu,2 Lucas Evangelista de Lima Terceiro,1 Jude E. Uzonna,2 *Yvonne Myal1,3,4

The authors have declared no conflicts of interest.


The authors wish to acknowledge the grant support from CancerCare Manitoba Foundation. Chidalu A. Edechi and Nnamdi M. Ikeogu contributed equally to the manuscript.


Each article is made available under the terms of the Creative Commons Attribution-Non Commercial 4.0 License.


The underlying mechanisms of metastasis in patients with breast cancer is still poorly understood. Approximately 6% of patients with breast cancer present with metastasis at the time of diagnosis. Metastatic breast cancer is difficult to treat and patients with breast cancer with distant metastasis have a significantly lower 5-year survival rate compared to patients with localised breast cancer (27% and 99%, respectively). During breast cancer progression, tumour cells first metastasise to nearby draining lymph nodes and then to distant organs, primarily bone, lungs, liver, and brain. In this brief review, the authors discuss breast cancer metastasis, the role of epithelial–mesenchymal transition and the contributions of the immune system to the metastatic process. The authors also briefly discuss whether there is any relationship between tumour size and metastatic potential, and recent advances in treatment for metastatic breast cancer. The studies highlighted suggest that immunotherapy may play a more significant role in future patient care for metastatic breast cancer.


Breast Cancer: From Detection to Treatment

Breast cancer is one of the most commonly diagnosed cancers among women.1 Despite advances in treatment for breast cancer, approximately 10% of women currently fail primary management strategies for early breast cancer and go on to develop recurrence, ultimately succumbing to the disease within 5 years. For those who present with late stage breast cancer, the odds of dying within that same timeframe increases to 30%.2 Furthermore, 6–10% of women diagnosed with breast cancer have Stage IV, or metastatic, breast cancer that has spread to other organs, primarily the lung, liver, brain or bone; 85% of breast cancer deaths are attributable to metastasis.2 Although several subtypes of breast cancer have now been identified, breast cancers are often categorised into four major molecular subtypes: luminal A and luminal B, based on oestrogen receptor (ER) and progesterone receptor (PR) status; human epidermal growth factor receptor 2 (HER2)-positive; and basal-like or triple-negative breast cancers (TNBC), which are ER-, PR-, and HER2-negative.3

Detection of breast cancer can be through self-detection but, most often, breast cancers are identified by mammographic screening4 followed by breast biopsy.5 Prolactin-inducible protein, mammaglobin, and GATA-3 are used to determine whether an unknown metastatic cancer is of breast origin.6 Additionally, there are blood-based assays which detect breast cancer-associated biomarkers such as carcinoembryonic antigen (CEA).7 Treatment for breast cancer primarily comprises surgical intervention, followed by endocrine (hormonal) therapy, chemotherapy, radiation therapy, or some combination of these therapeutic approaches.8 Endocrine therapy is recommended in patients with breast cancer with hormone (oestrogen and progesterone) receptor-positive (HR-positive) tumours.8 The menopausal status of the patient plays a major role in the decision to recommend a particular therapeutic strategy.9 While tamoxifen is the drug of choice for premenopausal patients,9 aromatase inhibitors (such as letrozole) are preferred for postmenopausal patients.10 For patients with HR-negative breast tumours, chemotherapy is the treatment of choice and is often recommended in patients with TNBC and HER2-positive breast cancer.11 Radiation therapy may also be used to further shrink breast tumours after surgical intervention.12

Patients with early-stage and localised breast cancer generally have a good prognosis with approximately 99% of patients surviving over a 5-year period.1 However, a recent study showed that at the cessation of 5 years of endocrine therapy, the risk of breast cancer recurrence remained relatively significant even after 15 to 20 years.13 This observation suggests that 5 years of treatment is not sufficient and that a longer period of therapy should be considered to prevent breast cancer recurrence. In this review, the authors give a brief overview of the existing challenges metastatic breast cancer presents and highlight some recent advances in treatment strategies.


Metastasis is a series of events that involve the invasion of the basement membrane at the primary tumour site, movement of the tumour cells into circulation, and subsequent dissemination to other organs.14 During metastasis, cells lose their epithelial nature and assume a mesenchymal phenotype, and extracellular matrix proteins in the basement membrane are degraded by proteolytic enzymes, such as matrix metalloproteinases.14 Collectively, these processes allow the cancer cells to leave the primary tumour site and escape into the circulation (blood or lymphatics) in a process known as intravasation. Generally, breast cancer first spreads to lymph nodes in close proximity to the breast through the lymphatic system, while metastasis to distant organs usually occurs via the blood.15 Once in circulation, the breast cancer cells, now referred to as circulating tumour cells (CTC),16 migrate to different organs in the body. CTC are often scarce in non-metastatic breast cancer but higher in advanced breast cancer disease.17 Some markers used for CTC detection include the epithelial cell adhesion molecule, an epithelial cell marker. However, cancers can alter their expression of these markers; for instance, by undergoing epithelial–mesenchymal transition (EMT).18CTC are now being utilised for the early detection of breast cancer19 and the evaluation of metastatic risk in patients.17 However, there are controversies concerning the detection of CTC in the blood because of the absence of accurate and specific markers.18 Alternatively, other biomarkers, such as exosomes, may also be used for determining diagnosis or prognosis, or to predict response to therapy.20 When CTC move out of the blood to metastatic sites in a process known as extravasation,21 they are then referred to as disseminated tumour cells.16 At these metastatic sites, the disseminated tumour cells form new tumour foci and spread throughout the affected organ, ultimately contributing to patient mortality. It is believed that metastasis involves an interplay between cancer cells and the metastatic tissue or organ, as some cancer cells are able to better form metastasis than others and some metastatic organs are more receptive to cancer cells than others.22 The metastatic process is reviewed by Lambert et al.14

Epithelial–Mesenchymal Transition

EMT is the process by which epithelial cells acquire a mesenchymal phenotype during cancer development.23EMT is induced by key transcription factors such as Snail, Slug, Twist, and ZEB114 and is characterised by loss of cell–cell adhesion, apical–basal polarity, and expression of epithelial markers such as E-cadherin and cytokeratin, while mesenchymal markers, including N-cadherin and vimentin, are upregulated.24 This shift from an epithelial to a mesenchymal phenotype enables the cancer cells to detach from the primary tumour, invade the basement membrane, and migrate to a distant organ and establish there.25 Following transition, the cancer cells then acquire the ability to initiate tumour formation, which is a typical feature of cancer stem cells.26 This tumour-initiating ability is a critical step in the metastatic process as it ensures that the disseminated breast cancer cells are capable of forming tumours at metastatic sites.14 Across different breast cancer subtypes, TGF-β signalling has been shown to be important for EMT and is potentially a master regulator of this process in breast cancer cells. This has been reviewed by Singh et al.27

The Immune Response

The immune system plays a critical role in the progression of many cancers including breast cancer. Similar to certain components of the immune system that are known to participate in the prevention and elimination of cancer, other components of the immune system can promote cancer progression and metastasis.28Myeloid-derived suppressor cells (MDSC), alternatively activated (M2) macrophages, and regulatory T cells have been shown to secrete factors that suppress anti-tumour immune responses.29 MDSC secrete TGF-βand vascular endothelial growth factor (VEGF) which stimulate EMT and angiogenesis, facilitating tumour growth and metastasis.30 MDSC also release the anti-inflammatory cytokine IL-10: a potent suppressor of anti-tumour immune responses.30 Additionally, macrophages in the tumour microenvironment have been shown to display the M2 phenotype; M2 macrophages are important for wound healing and tissue repair.31Like MDSC, M2 macrophages release TGF-β, IL-10, and chemokines which promote breast cancer growth and metastasis.32 In addition to suppressing anti-tumour cytotoxic and helper T cells via cell-to-cell contact, regulatory T cells also secrete IL-10 which dampens anti-tumour immune responses.33 Studies also indicate that neutrophils, another group of immune cells, can enhance metastasis by inhibiting cytotoxic T cell function,34 secreting leukotrienes, and promoting the proliferation of tumour-initiating cells at the metastatic environment.35

Does Tumour Size Matter?

Although previous studies suggested that the relationship between tumour size and metastasis was linear, recent data from a large population study of more than 800,000 patients with breast cancer showed that it is not.36 This study showed that at the time of diagnosis, a patient with a tumour 7 cm in diameter has an approximately equal chance of having lymph node metastasis compared to a patient with a 15 cm tumour (71.8% versus 71.3%, respectively).37 The discrepancy between previous studies and the current study may be attributed to the small sample size and inaccurate methods of those previous studies. In addition to axillary lymph node metastasis, studies also show that larger tumour sizes correlated with worse clinical outcomes.38However, many patients with TNBC, especially the subset that express basal markers such as cytokeratin, do not follow this trend.36 Indeed, smaller basal tumours have been associated with more lymph node metastasis than non-basal tumours and had worse disease outcomes than expected; larger basal tumours were associated with better outcomes than expected.39 Most of the mutations found in the primary tumour of a patient with basal-like breast cancer were also found in metastatic cells of the patient, suggesting that the primary tumour cells already had the necessary features needed to metastasise.40 Other parameters such as biomarker expression, e.g., Ki67, were found to correlate with both lymph node metastasis and tumour size.41 It appears that size is not the only determining factor for metastatic spread; the subtype and intrinsic biology of the tumour may play critical roles as well.


The draining, or sentinel, lymph node in the axilla, which is located in close proximity to the breast tumour site, is usually the first site of metastasis.42 Breast cancer then spreads to distal sites, most frequently bone, lungs, liver, and the brain.43 Estimates from a recent study showed that at the time of diagnosis, patients with metastatic breast cancer were found to most frequently present with bone metastasis (3.28%), followed by lung (1.52%) and liver (1.20%) metastasis, while the brain was the least common site for metastasis (0.35%).44

Metastasis to Bone

Current understanding suggests that metastatic breast cancer cells are able to take advantage of the natural remodelling process in the bone to facilitate metastasis by disrupting the balance between formation and resorption of bone, leading to bone loss (osteolysis) or abnormal bone formation.45 One process for causing this disruption is by secreting factors to modulate their environment.46 Breast cancer cells have been reported to secrete IL-11 and matrix metalloproteinases which can stimulate osteoclasts to produce growth factors that, in turn, promote the growth and survival of the metastatic breast cancer cells in the bone.46Interestingly, results from recent studies also suggest that prolactin overexpression in breast tumours can shorten the time to development of bone metastasis and contribute to osteolysis induced by the metastatic breast cancer cells.47 Among all breast cancer subtypes, patients with luminal breast cancer have the highest rate of bone metastasis.48

Metastasis to the Lungs

Breast cancer cells released from the primary tumour may also spread to the lungs.49 Lung metastasis is usually observed 5 years after initial breast cancer diagnosis, with >60% mortality rate following lung metastasis.49 The subtype of breast cancer affects the frequency of lung metastasis. Patients with TNBC were reported to be more likely to develop lung metastasis compared to other subtypes.48 The development of lung metastasis in patients with breast cancer may be because of an inherent ability of breast cancer cells to the lungs, or an ability to interact with the lung microenvironment. Premalignant breast cells have been shown to invade the lungs after injection into the blood, suggesting that breast cancer cells may have some intrinsic ability to establish in the lungs.50 It has been shown in vitro that the migration and proliferation of breast cancer cells were stimulated by the conditioned medium of the lungs, suggesting that factors from the lungs promote lung metastasis. One such factor identified was selectin, a cell adhesion molecule.51

Metastasis to the Liver

Another common site for breast cancer metastasis is the liver. Liver metastasis leads to impairment of liver function with serious outcomes, and without treatment intervention life expectancy is <8 months.52 Patients with HER2-positive breast cancers show the highest incidence of liver metastasis.48

Metastasis to the Brain

Although less common, breast cancer can also metastasise to the brain. Patients with breast cancer and brain metastasis have poor prognosis, display neurological defects, and do not respond well to therapy.53Due to more successful treatment of the primary tumour, patients with breast cancer live longer, and brain metastasis more frequently becomes evident later in the disease process.54 The propensity of breast cancer to metastasise to the brain seems to depend on the breast cancer subtype.55 Brain metastasis occurs in approximately 50% of patients with TNBC, and 33% and 14% of patients with HER2-positive and HR-positive breast cancer, respectively.48


Standard Therapeutic Drugs

The treatment strategies utilised for patients with metastatic breast cancer depend on several factors. These factors are often based on two considerations: the breast cancer subtype and the stage of the disease. Generally, patients with HR-positive breast cancer are treated with endocrine therapy, patients with HER2-positive breast cancer are treated with anti-HER2 antibody therapies, such as trastuzumab, while triple-negative tumours are typically treated with chemotherapy.3 The initial treatment regimen for patients with metastatic HR-positive breast cancer includes endocrine therapy in combination with a cyclin-dependent kinase (CDK) 4/6 inhibitor, such as abemaciclib. Patients with resistance to endocrine therapy are treated with chemotherapy.3 For patients with HER2-positive breast cancer, the first line of treatment includes a combination of an anti-HER2 antibody therapy, such as trastuzumab, and a chemotherapy, e.g., a taxane. If this initial treatment is unsuccessful, trastuzumab emtansine, an antibody–drug conjugate, is then administered.3 If this treatment also fails, continuous use of the HER2-targeted therapy may be recommended, in combination with a different chemotherapeutic agent. Unlike HR- and HER2-positive breast cancers, TNBC are only treated with chemotherapy because of a lack of established molecular targets, as reviewed by Waks et al.3

New Therapeutic Drugs

Several new therapeutic agents have been recently approved by the U.S. Food and Drug Administration (FDA), while a number are still undergoing clinical trials. Sacituzumab govitecan is an antibody–drug conjugate, currently undergoing testing in clinical trials, which has shown positive effects in previously treated patients with advanced TNBC.56 Another promising drug is atezolizumab, an inhibitor of programmed death-ligand 1, and nanoparticle albumin-bound-paclitaxel, which was shown to enhance progression-free survival in patients with breast cancer.57 To treat patients with metastatic breast tumours harbouring the BRCA1/2 mutations, poly(ADP-ribose) polymerase (PARP) inhibitors, such as olaparib, were recently approved by the FDA.58 PARP inhibitors are used to counteract the DNA repair brought about by PARP, to enhance the sensitivity of cancer cells to DNA-damaging anti-cancer therapies, and ultimately lead to cell death.59 However, many of these drugs are only successful in extending the patients’ lives for a short period of time. Response rates are often poor, and many patients develop serious side effects. A study reported that among histological subtypes, patients with invasive lobular carcinoma had increased progression-free survival compared to patients with invasive ductal carcinoma; however, there was no difference in overall survival.60 Across molecular subtypes, patients with HR-positive/HER2-positive breast tumours had better survival outcomes, while those with TNBC had worse outcomes.61 Another challenge is that following systemic therapy, a population of dormant breast cancer cells may persist and subsequently lead to relapse.14 This situation is further complicated by the cytotoxic treatments used against breast cancer mainly targeting highly proliferating cells with minimal effects on dormant cells.14

Immunotherapy: Homing in on our Immune Response

Immunotherapy is a treatment strategy that harnesses the ability of the immune system to keep diseases, including cancers, at bay. In recent years, there have been some successes in using immunotherapy to treat certain type of cancers such as melanoma, which is considered to be an immunogenic cancer, capable of eliciting an immune response.62 Breast cancer was previously not considered to be an immunogenic cancer, but it has now been shown that the presence of immune cells in some breast cancers is of prognostic and therapeutic significance.62 Breast cancers with greater influx of tumour-infiltrating lymphocytes tend to respond better to neoadjuvant chemotherapy compared to those with fewer tumour-infiltrating lymphocytes.29

Recently, some immunotherapeutic approaches have been assessed for the treatment of a limited number of patients with breast cancer. These include the use of tumour antigen-specific antibodies and adoptive transfer of activated immune cells, such as natural killer cells, dendritic cells, and T cells.28 A recent study was the first to demonstrate no signs of cancer in a patient with metastatic breast cancer following treatment by adoptive transfer of activated patient-derived tumour-specific T cells.63 Pembrolizumab, an anti-PD1 antibody, has been shown to be effective for patients with metastatic TNBC in clinical trials.64 Vaccines are also being explored as another treatment strategy. The use of recombinant HER2 protein in patients with advanced HER2-positive breast cancer was shown to induce an anti-tumour immune response and benefit a limited number of patients.65 The use of chimeric antigen receptor T cells is another immunotherapeutic strategy currently being developed for treatment of breast cancer. Studies using chimeric antigen receptor T cells engineered to target the mucin 1 protein expressed on breast cancer cells have shown promising preclinical results66 and this therapy is currently undergoing clinical trials.67 Major challenges with these approaches include the cost of treatment and the difficulty in isolating sufficient activated tumour-specific T cells from patients. However, efforts are being made to reduce these challenges through the utility of immune cells from unrelated donors without tissue rejection.68 Some current therapeutic approaches are summarised in Table 1.

Table 1: Examples of current therapeutic approaches for metastatic breast cancer patients.
CDK: cyclin-dependent kinase; HER2: human epidermal growth factor receptor 2; HR: hormone receptor; PD-L1: programmed death-ligand 1; TNBC: triple-negative breast cancer.


The wide degree of heterogeneity that exists among breast cancers presents many challenges for both clinicians and patients. There are still significant gaps in knowledge about the metastatic process during breast cancer progression, including: why different breast cancer subtypes preferentially metastasise to specific organs; why tumour size does not always matter; and why some breast cancers trigger an immune response while others do not. Advances in the understanding of the interaction between several cancers and the immune system could lead to the use of immunotherapy as a viable option for the treatment of some patients with breast cancer with metastatic disease. There is also a need for greater understanding of key signalling pathways. However, a multidisciplinary approach to research is warranted to address these gaps in knowledge and to develop effective strategies to benefit a large number of patients. Furthermore, current comprehensive guidelines for the treatment of metastatic breast cancer provided by key European and American societies, such as the European Society for Medical Oncology (ESMO)69 and the National Comprehensive Cancer Network (NCCN),70 are largely similar in their recommendations. However, some discrepancies do exist, highlighting that further research is warranted to fully determine which therapies are most effective and beneficial for patients in the long term.

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