Breast Cancer Immunotherapy: An Update.

The immune system plays a major role in cancer surveillance. Harnessing its power to treat many cancers is now a reality that has led to cures in hopeless situations where no other solutions were available from traditional anticancer drugs. These spectacular achievements rekindled the oncology community's interest in extending the benefits to all cancers including breast cancer. The first section of this article reviews the biological foundations of the immune response to different subtypes of breast cancer and the ways cancer may overcome the immune attack leading to cancer disease. The second section is dedicated to the actual immune treatments including breast cancer vaccines, checkpoint inhibitors, monoclonal antibodies, and the "unconventional" immune role of chemotherapy.

Introduction

Breast cancer is the most common cancer in women with an estimated 268 670 new cases in the United States in 2018.[1] It is also the second leading cause of cancer death in women. Fortunately, with advances in detection and treatment, death rates from breast cancer are declining. More recent advancements in breast cancer therapy using novel mechanisms involving actionable cancer mutations and the body’s immune system have opened up new avenues for reducing the death rate further. Many of the obvious successes in immunotherapy have been in the field of melanoma, renal cancer, lung cancer, and others that have traditionally been known to be immunogenic. However, these are not the only cancers in which strides in immunotherapy are being made. Breast cancer is one cancer that, although not originally thought to be immunogenic, has had many encouraging results in the past few years. We aim to provide a succinct overview of breast cancer immunotherapy as well as possible future directions.

Background

The basis for immunotherapy in cancer has revolved around the concept of immunogenicity. For a long time, breast cancer has been considered nonimmunogenic. However, the role of the immune system in the emergence of breast cancer has been firmly established.[2-8] Random or inherited genetic and epigenetic abnormalities confer proliferative and/or survival advantages on certain cells. These incipient cancer cells face internal and external control mechanisms including those from the immune system. By targeting the new antigens created by these genetic changes, the immune system plays a central role in cancer control that can be host-protective or tumor promoting. A mutated gene leads to the production of a neoantigen when it is transcribed then translated, highlighting the autoantigenicity of self-antigens as observed in model protein antigens.[9]

Epitopes from the neoantigen are presented after processing by the mammary epithelial cells in association with major histocompatibility complex (MHC) class I (MHC-I) on their surface. When an antigen-presenting cell (APC) encounters a neoantigen released from debris of cancer cells or secreted in the environment, it internalizes it via several mechanisms including endocytosis. The antigen resurfaces again after processing on the MHC class II (MHC-II) receptors and can be recognized by helper T-cell receptors (TCR). Helper T (TH) cells stimulate and drive cytotoxic T cells (Tc) and B cells to further maturation. T-cell maturation, proliferation, and survival require antigen-independent costimulatory signals from APCs. If the costimulatory signal is lacking, then the process of activation will be ineffective and may lead to Tc anergy. Once activated, Tc can attack the target cell by several mechanisms, including TCR-MHC-I recognition and binding. This leads to secretion of cytotoxic granules including perforin that result in cell lyses and demise.[10] Another mechanism by which Tc can attack target cells is via FAS receptors on Tc that bind FASL on the target cell leading to caspase 3 and 8 activation in the target cell and eventually apoptosis.[11] To ensure effective immune regulation, the very same APCs that send costimulatory signals (through CD27, CD28, CD40, OX40, 4-1BB, GITR, and ICOS surface proteins on T cells) to intensify the activation of naïve T cells also send inhibitory signals (through CTLA-4, PD-1, and LAG-3) to the already activated T cells and natural killer (NK) cells when the immune response has to wind down. The activated T cell starts synthesizing CTLA-4, which has higher affinity for B7 and competes with the stimulatory B7-CD28 binding.[12] This mechanism prevents overstimulation by transient T-cell activation (Figure 1).

Figure 1.

Antigen-presenting cells (APCs) process tumor-associated antigens (TAAs) and present them in combination with MHC surface proteins to T-cell receptor (TCR) on T-helper cells (MHC-II) and some CD8+ T cells (MHC-I). In the beginning of the immune reaction, costimulatory signals (CD27, CD28, CD40, OX40, 4-1BB, GITR, and ICOS surface proteins on T cells) help intensify the activation of naïve helper or cytotoxic T cells. As the immune reaction reaches its goal of eliminating the transformed cells, inhibitory signals (CTLA-4, PD-1, and LAG-3) help wind down T-cell activation. The expression of the inhibitory molecules by the transformed cells or other cells in the tumor microenvironment leads to local immunosuppression and the persistence of cancer cells. Inhibitory monoclonal antibodies (MAbs) targeting CTLA-4, PD-1, or PD-L1 have opened the way to a new era in IO. Targeting stimulatory pathways with agonist MAbs is being explored by multiple clinical trials (see below). Bispecific antibodies (BsABs) target T-cell surface receptors such as CD3 and TAA and recruit other effector cells through the Fc receptor such as macrophages or natural killer cells.

The interaction between the immune system and incipient cancer cells, also called immunoediting, goes through 3 phases: elimination, equilibrium, and escape.[13-15] Elimination is supported by a wealth of experimental evidence in animals and humans. The innate and adaptive arms of the immune system recognize incipient cancer cells by the new antigens (resulting from mutations or translocations) presented on their surface in association with MHC-I or by the distress signals usually expressed by transformed cells that have undergone chromosomal changes (aneuploidy or hyperploidy)[16,17] and eliminate them. Equilibrium is reached when the immune system fails to eliminate the transformed cells but stops them from progressing further. This can be conceived as the dormancy phase of primary cancer development. This phase is mediated by equilibrium between cells and cytokines that promote elimination (IL-12, IFN-γ, TNF-α, CD4 TH1, CD8+ T cells, NK cells, γδT cells) and those that promote persistence of the nascent tumor (IL-23, IL-6, IL-10, TGF-β, NKT cells, CD4 Th2, Foxp3+ regulatory T [Treg] cells, and MDSCs).[18-20] Monocytes play an important role in this process. Under the influence of the tumor microenvironment (TME), they may differentiate into pro-inflammatory M1 or anti-inflammatory M2 types.[21,22] Immune escape of cancer cells occurs by different mechanisms. In HR-positive breast cancer, the absence of strong tumor antigens and low expression of MHC-I allow the tumor to progress unnoticed by the immune system.[23] Estrogen plays an immunosuppressive role in the TME that promotes tolerance of the weakly immunogenic cancer. Most immune cells including macrophages, T and B lymphocytes, and NK cells express estrogen receptor (ER).[24] In presence of estrogen, the immune response is polarized to Th2− rather than Th1-effector immune response.[25] In HER2-positive cancer cells, MHC-I presentation is inversely correlated with HER2 expression.[26] Triple-negative breast cancers (TNBC) exhibit a spectrum of MHC-I presentation and strong tumor antigen expression, but immune escape in this subtype is mostly related to the development of the immunosuppressive TME (Tregs, MDSCs, PD-1/PD-L1).

Although it is true that single-transformed cells may remain dormant in inactive noncycling state, some transformed cells may continue dividing until they reach equilibrium between the newly produced cells and those undergoing cell death. These 2 models (of dormant single cells or a small cluster of transformed cells that remain microscopic and stay dormant) may also apply to disseminated tumor cells that land in a new environment and have to renegotiate a license to grow with the new TME.[27]

Factors promoting immune escape

Many factors play a role in tilting the balance established during the equilibrium phase toward tumor progression. Aging is associated with reduced production of new B and T lymphocytes in the bone marrow and the thymus, respectively, and with decreased function of the existing mature lymphocytes.[28] Systemic inflammation associated with aging and the local pro-inflammatory microenvironment in the breast is incriminated in promoting the cancerous transformation of mammary stem cells that have been primed by losing tumor suppressor genes.[20,29] Pro-inflammatory cytokines (TNF-α and IL-6) are associated with overexpression of COX2 and the aromatase enzyme,[30] which lead to increased local concentrations of estrogens. Estrogens induce the expansion of Tregs and MDSCs, as well as the inhibition of antigen-presenting cells.[31-34] In addition to the gradual decline of the immune system, dietary, commensal microbiota, use of antibiotics, procreational and hormonal factors, all play some role of variable importance in tilting the balance from equilibrium to escape.[35-38]

Immune escape, the angiogenic switch, and cancer cell dissemination

The immune escape and angiogenic switch may be closely connected. Tumor-associated macrophages (TAMs; and other immune and microenvironment cells) release proangiogenic factors that play an important role in triggering the angiogenic switch that leads to the expansion of the tumor mass (Figure 2).[39]

Figure 2.

Immune and angiogenic dormancy in maintaining the cancer at a microscopic size. (A) Once the tumor undergoes immune escape and the angiogenic switch is turned on, the tumor grows locally and spreads metastases. In this model, DTCs are released at a later stage because DTCs do not gain access to the bloodstream until the tumor has acquired its own vasculature. (B) Another model stipulates that dissemination of cancer cells may occur very early in the beginning of the nascent cancer and continues throughout its growth and development. In this model, the role of immune escape is more important than the role of the angiogenic switch because microscopic tumors (and even in situ tumors) may spawn DTCs/micrometastasis before the angiogenic switch has taken place. DTCs indicate disseminated tumor cells.

Tumor progression is traditionally conceived in a linear fashion suggesting that once the tumor has undergone immune escape and turned the angiogenic switch on, it will grow locally and release cancer cells (disseminated tumor cells = DTCs) into the circulation (Figure 2A). Accumulating evidence suggests that DTCs may be released with the very early stages of transformation even during the in situ phase and before the tumor has established its own vasculature or before becoming clinically detectable (Figure 2B).[40-42]

Breast cancer stem cells and immune escape

Two models have been proposed to explain the emergence of breast cancer and its dissemination. The stochastic model stipulates that all cancer cells in a tumor are potentially capable of being tumor-initiating cells and the hierarchical model that stipulates the presence of a distinct cell population called cancer stem cells (CSCs; the concept of CSC is controversial[43,44]) endowed with the self-renewal capacity and tumor initiation function is necessary for the emergence and progression of cancer. The hierarchical model states that CSCs are capable of asymmetric division that gives rise to CSCs that join the stem cell compartment and to other cells that continue proliferating and differentiating allowing the expansion of the tumor mass while losing their self-renewal potential (transit-amplifying cells).[45] Cancer stem cells are characterized by being metabolically quiescent and long-lived. They are responsible for the propagation and dissemination of cancer and resistance to classical cytotoxic treatments, contrary to the rest of tumor cells that are short-lived and possess limited proliferative capacity and are sensitive to cytotoxic agents.[46-48] Recently, the discovery of phenotypic plasticity allows reconciling these 2 models by establishing the reversibility of differentiated cells to a stem cell phenotype in certain conditions. Based on the phenotypic plasticity model, stem cell function is the result of the interaction between the genetic make-up of a cancer cell and its microenvironment or niche.[44]

The immune system as a part of the CSC niche

Cancer stem cell niche is a distinct part of the TME.[49] It plays a major role in protecting CSCs from the immune system and in maintaining their plasticity. The frequent success of transplantation experiments of cancer cells (regardless of their stemness characteristics or the size of the inoculate) in extremely immune-deficient models and their failure in immune-competent animals suggest a major role for the immune system in facilitating or hindering cancer cell growth, respectively.[50]

This fascinating concept suggests that the niche (of which the competence the immune system is an important part) shapes cancer cell stemness[45] and determines the fate of dormant DTCs or microscopic tumors. Myeloid-derived suppressor cells (MDSCs), tumor- TAMs and tumor-associated neutrophils (TANs) recruited by cancer-released cytokines and chemokines participate in the local immune suppression in TME.[51,52] The TAMs and TANs secrete TNF-α that induces the expression of Slug, Snail, and Twist transcription factors responsible for the induction of epithelial–mesenchymal transition in transformed epithelial cells that acquire CSC characteristics. Hypoxia, resulting from the increase in the tumor mass beyond certain size, has a CSC-protective effect against chemotherapy and radiotherapy. It activates the hypoxia-inducible factor 1α (HIF1α) pathway, vascular endothelial growth factor (VEGF), and TGF-β. The expression of TGF-β in the TME and the activation of WNT lead to an undifferentiated state in tumor cells,[53] whereas the expression of VEGF stimulates tumor angiogenesis. The importance of the permissive role of the innate and adaptive immune systems in establishing distant metastases by DTCs is increasingly recognized.[49]

Assessment of Breast Cancer Immunogenicity

Traditional pathology and immunohistochemistry, gene expression profiling, RNA sequencing, and combined scores have been used to assess the immunogenicity of breast cancer. Traditional pathology tools allow the assessment of breast cancer immunogenicity by studying the presence of tumor-infiltrating lymphocytes (TILs) and assessing their types and correlation with survival and recurrence. While TILs were not found to have a prognostic value in the overall breast cancer population or ER-positive/human epidermal growth factor receptor 2–negative (ER+/HER2−) patients, TILs were found to have a prognostic value for disease-free survival (DFS) and overall survival (OS) in TNBC.[54] In patients with TNBC who had residual disease after neoadjuvant chemotherapy, the presence of TILs was found to be associated with better OS as well as with metastasis-free survival. In ER-negative breast cancers, TILs, specifically CD8+ lymphocytes, were associated with better breast cancer–specific survival.[54,55] The presence of CD8+ lymphocytes in patients with ER-negative breast cancers was also related to longer DFS.[55] In general, the presence of TILs was positively correlated with MHC-I expression and inversely correlated with ER expression. The more immunogenic the breast cancer, the higher the concentration of TILs will be. Hence, it is not surprising that HR-positive breast cancer is considered the least immunogenic.

Mutational load and neoantigens

Recent advances in genomics and proteomics allow the detection of neoantigens that underlie immunogenicity in breast cancer and shed light on possible targets for therapy.[56,57] Immunogenicity of a tumor is evaluated by the assessment of its antigenicity and the latter is evaluated by assessing its mutagenicity. Mutational load, the average number of somatic mutations per cancer cell, is associated with antigenicity and is, in general, lower in breast cancer compared with other tumors such as melanoma or lung cancer. However, major differences exist between different subtypes of breast cancer; TNBC has the highest mutational load compared with HR-positive breast cancers[58,59] and high mutational load is associated with better prognosis in TNBC and HER2+ compared with low mutational load in the same type of breast cancer (see below). Conversely, higher mutational load is associated with higher concentrations of TILs and with poor prognosis in HR-positive breast cancer. Mutational load continues increasing in metastatic breast cancer (MBC) but TILs, PD-1, and PDL-1 expression decreases, very likely as a result of immune exhaustion and not because of decreased immunogenicity in advanced disease as suggested by Luen et al.[60] Some specific mutations in DNA repair mechanisms such as those in the BRCA1/2 and MMR genes are associated with high mutational loads that can be localized (kataegis) or generalized.[61,62] High mutational load is associated with high rates of neoantigens, which predict OS and response to checkpoint inhibitors.[56,57,63-65]

TILs and immune response

In assessing response to neoadjuvant treatment, the benefit of the presence of TILs can be seen here as well. Breast cancers with higher levels of TILs have better responses to neoadjuvant chemotherapy.[7] In patients with HER2+ or TNBC, those with >60% TILs treated with an anthracycline plus taxane combination were more likely to have a pathologic complete response (pCR) and the rates of pCR were even higher when carboplatin was added to the treatment regimen.[8] The ER-negative breast cancers that are lymphocyte-rich have far greater pCR rates when treated with neoadjuvant anthracycline-based chemotherapy compared with patients with lymphocyte-poor ER breast cancers.[66] HER2+ breast cancers with TILs were associated with better DFS as well as OS in response to treatment with anthracyclines.[2] There was a significantly associated decreasing risk of distant recurrence in patients being treated with adjuvant chemotherapy simultaneously with trastuzumab in HER2+ breast cancer for every 10% increase in TILs.[3] Moreover, irrespective of whether or not a patient received systemic adjuvant chemotherapy, TILs and immune signatures were associated with better prognosis in HER2+ breast cancer.[67] In patients with HER2 overexpression, a higher CD8+ infiltrate was seen after chemotherapy and this was associated with improved relapse-free survival.[68]

Strategies to Harness the Power of the Immune System

Several strategies have been used to harness the power of the immune system and redirect it to eradicate breast cancer or to induce immune dormancy:

Breast cancer vaccines;

Monoclonal antibodies (MAbs);

Antibody-drug conjugates (ADCs);

Checkpoint inhibitors;

Stimulatory molecule agonist antibodies;

Combination immunotherapy trials;

Enhance the immune-mediated effect of chemotherapy.

Breast cancer vaccines

Breast cancer vaccines are used for primary or secondary prevention and some are therapeutic. Several strategies have been used including peptide vaccines, recombinant protein vaccines, dendritic cell (DC) vaccines, whole tumor cell vaccines, DNA vaccines, and recombinant viral vectors vaccines.

They are all designed to stimulate an intrinsic antitumor response targeting tumor-associated antigens (TAAs). Tumor-associated antigens that are specifically recognized by T cells include HER2, mucin 1 (MUC1), carcinoembryonic antigen, sialyl-Tn (STn), human telomerase reverse transcriptase (hTERT), Wilms tumor gene (WT1), and tumor-associated carbohydrate antigens (TACAs).[69] The antigens where current studies are primarily focused around include HER2, MUC1, and TACAs. DNA vaccines will not be discussed in this review.

HER2-targeted vaccines

As for the use of HER2 in vaccine developments, there have been a few attempts involving the E75, GP2, and AE37 peptides. Nelipepimut-S (NeuVax) is a combination of E75, a peptide from the extracellular domain of HER2 and granulocyte-macrophage colony-stimulating factor (GM-CSF); it stimulates cytotoxic T lymphocytes and CD8+ memory cells with high affinity for HLA-A2/A3. However, the immunity induced by the E75 vaccine waned after 6 months from initial vaccination requiring a booster given at 6 months from completion of the primary vaccination.[70] NeuVax was tested in a phase I/II trial and showed improvement of DFS in HER2-positive breast cancer patients.[71] The study enrolled 187 patients with early-stage breast cancer deemed at high risk for recurrence. Patients received 6 injections of NeuVax after tumor resection with standard of care (chemotherapy or radiation therapy [RT]) as indicated. The 5-year DFS was 89.7% for the vaccinated group versus 80.2% for the controls (P = .08). When the optimally dosed cohort was considered, DFS was increased to 94.8% versus 80.2% (P = .05). Apparently, the induction of cytotoxic T lymphocytes was crucial for the response to NeuVax as only 1 recurrence was observed in 30 patients (3%) who achieved cytotoxic T lymphocytes above the mean, compared with 8 of 56 (14%) for patients with levels of cytotoxic T lymphocytes below the mean.[72] A phase III registration PRESENT trial is evaluating E75 in 758 early-stage, node-positive HLA-A2/A3 patients with low to intermediate HER2 expression with no evidence of disease after standard treatment. Patients are randomized to GM-CSF with E75 or GM-CSF with placebo, receiving 6 monthly injections, followed by a booster vaccination every 6 months for 3 years. The primary end point is DFS at 3 years.[73]

Work with the GP2 peptide is currently ongoing in a phase II clinical trial where vaccines containing GP2, a class I epitope derived from the HER2 transmembrane domain, is combined with GM-CSF and then compared with treatment of patients with GM-CSF only. Interim analysis presented in 2009 was already showing a decreased recurrence rate at 17.9 months in a group of patients treated with GP2 and GM-CSF (VG) versus GM-CSF alone (CG), 7.4% (2/27) compared with 13% (3/23), respectively (P = .65).[74] At 34-month (1-60) median follow-up, DFS was compared in the intent to treat (ITT) (85% VG versus 81% CG, P = .57) and per treatment (PT) (94% VG versus 85% CG, P = .17) populations. In patients with HER2 overexpression (51 VG and 50 CG) DFS was 94% VG versus 89% CG, P = .86 (ITT) and 100% VG versus 89% CG, P = .08 (PT).[75]

The premise behind the AE37 vaccine is that it stimulates a CD4+ T-lymphocyte response that could potentially result in a more sustained immune response. The current data from clinical trials suggest that this vaccine has an effect on the risk of recurrence.[76] The trial enrolled 298 patients: 153 received AE37 + GM-CSF and 145 received GM-CSF alone. At the time of the primary analysis, the recurrence rate in the vaccinated group was 12.4% versus 13.8% in the control group (relative risk reduction = 12%, hazard ratio [HR] = 0.885, 95% confidence interval (CI) = 0.472-1.659, P = .70). The Kaplan-Meier–estimated 5-year DFS rate was 80.8% in vaccinated versus 79.5% in control patients. In planned subset analyses of patients with IHC 1+/2+ HER2-expressing tumors, 5-year DFS was 77.2% in vaccinated patients (n = 76) versus 65.7% in control patients (n = 78) (P = .21). In patients with TNBC (HER2 IHC 1+/2+ and hormone receptor negative), DFS was 77.7% in vaccinated patients (n = 25) versus 49.0% in control patients (n = 25) (P = .12).[77] Although the trial was negative for the whole population, the results in the triple-negative subset of patients were encouraging and warrant further investigation. Another approach to HER2-positive early breast cancer was the use of the patients’ stimulated DCs. Monocytic DC precursors harvested by apheresis are pulsed with 6 HER2 MHC class II–binding peptides then given back to the patients as injections into the lymph nodes, the breast lesions, or both, weekly for 6 weeks prior to surgery. A total of 54 patients (44 with ductal carcinoma in situ [DCIS] and 12 with invasive ductal carcinoma) were enrolled in the study. There was no difference in the immune response by injection site. Patients with DCIS reached higher rate of pCR (28.6%) compared with those with invasive cancer (8.3%).[78] The failure of therapeutic vaccines and the success of this vaccine and other cancer prevention vaccines are attributed to the robustness of the immune system in the early stage or the preinvasive setting, making their use for breast cancer prevention in high-risk populations a promising next step.[79]

MUC1-targeted vaccine

The presence of high levels of antibodies to specific glycoforms of the MUC1 antigen has been shown to be associated with reduced rates and delay to metastasis in patients who have early-stage breast cancer.[80] One of these particular glycoforms, STnMUC1, has already been used in a phase III trial in the form of the vaccine Theratope (STnMUC1, keyhole limpet hemocyanin, and the adjuvant Detox-B). Given as a single agent, Theratope did not show any improvement in survival. However, when given along with endocrine therapy, there was a demonstrated improvement in time to progression and OS.[81] The reactivity of antibodies to MUC1 glycoforms might still be deceptive and can be related to an artifact rather than a true immune response to MUC1. The example of anti-Gal alpha (1,3) Gal antibodies is instructive. These antibodies are observed to react with mucin 1 (MUC1) found on the surface of human breast cancer cells.[82] Natural occurring anti-Gal alpha (1,3) Gal antibodies found in all human serum can react with self-peptides (MUC1) expressed in large amounts on the surface of tumor cells, but not on normal cells. These findings are of interest and serve to explain reported findings that human cells can, at times, express Gal alpha (1,3) Gal; in reality, such expression is suggested as an artifact in that anti-Gal alpha (1,3) Gal antibodies react with mucin peptides.[82] However, some antibodies display exquisite specificity, like those directed toward the Thomsen-Friedenreich (TF) antigen.[83] The TF antibodies may arise in the postpartum period against carbohydrate structures expressed on the cell walls of the gastrointestinal flora and, presumably, may provide an early barrier against TF-carrying tumor cells.

Tumor-associated carbohydrate antigens

The widely used regimen of neoadjuvant chemotherapy is demonstrated to stimulate the immune response to TACA in some patients.[84] Small retrospective studies have suggested that postchemotherapy lymphocyte infiltrates could be associated with better outcomes in patients who did not reach pCR.[84] The high levels of anti-TF antibody before surgery is another example in which antibody targeting is associated with a better survival of patients with stage II breast cancer.[85] This may indicate that the selection of immunopotentiating regimens of neoadjuvant chemotherapy might be beneficial for the host in conjunction with the functional activity of natural anticancer antibodies.

Because tumor tissue rejection is the goal of cancer immunotherapies, broad-spectrum TAAs, such as TACAs, are plausible targets once the problem of their low immunogenicity is solved.[86] The fact that multiple proteins and lipids on the cancer cell are modified with the same carbohydrate structure creates a powerful advantage for TACAs as cancer targets in immunotherapy strategies. Thus, targeting TACAs has the potential to broaden the spectrum of target pathways recognized by the immune response, thereby lowering the risk of developing escape variants due to the loss of a given protein or carbohydrate antigen. Although TACAs are poor immunogens, certain investigators succeeded in eliciting cytotoxic antibodies reactive with naturally occurring forms of TACA using molecular mimicry to generate peptide mimotopes of TACA (carbohydrate mimetic peptides [CMPs]). Vaccination of mice with TACA peptide mimotopes reduced tumor growth and prolonged host survival in a murine tumor model.[87] The first reports of this strategy in humans are promising and trials exploring their role in different types of breast cancer are underway.[88]

Multivalent vaccines comprising 2 or more candidate proteins are considered to substantially enhance the efficacy of vaccination against breast tumors. The enhancement in antitumor effect using a multivalent vaccination approach would be achieved on 2 levels: (1) by increasing the strength of immune response against arising tumor due to activation of a larger T-cell repertoire comprising multiple T-cell lineages reactive to more than one tumor-specific target and (2) by covering a broader range of tumors, including those that do not express the target protein by a univalent vaccination approach such as HER2 or MUC1. In addition, a multivalent vaccine will have the potential to target tumors that have lost or downregulated expression of one or more proteins or acquired expression of alternate proteins due to transcriptional dysregulation during their evolution from normal to dysplastic, to carcinoma in situ, to invasive, and to metastatic stages of breast tumor evolution. In other words, a multivalent vaccine approach could apply greater multitarget immunological pressure both on early and evolving tumors. It will thereby cover a larger tumor variety and increase efficacy of prevention as well as provide more effective therapy by lowering the probability of tumor escape and generation of resistance to the vaccine. Such approaches are heading to the clinic.

In contrast to a multivalent approach, a pan-immunogen that elicits responses to several antigens but as a univalent vaccine can achieve the same end as a multivalent vaccine. Tumor-associated carbohydrate antigens are among the most challenging of clinical targets for cancer immunotherapy, but this difficulty can be overcome by CMPs. Carbohydrate mimetic peptides are sufficiently potent to activate broad-spectrum antitumor reactivity. However, the activation of immune responses against terminal mono- and disaccharide constituents of TACA raises concerns regarding the balance between “tumor destruction” and “tissue damage,” as mono- and disaccharides are also expressed on normal tissue. To support the development of CMPs for clinical trial testing, we have demonstrated in preclinical safety assessment studies in mice that vaccination with CMPs can enhance responses to TACAs without mediating tissue damage to normal cells expressing TACA[89] and are pursuing such an approach in multiple phase II trials. Particularly important is that these CMP-induced antibodies can overcome resistance to anoikis and drug resistance against breast cancer and enhance the efficacy of taxanes. This aspect might suggest that immunization with such CMPs can change the clinical paradigm in the neoadjuvant/adjuvant setting.

Monoclonal antibodies

Monoclonal antibodies are an integral part of our armamentarium in the fight against cancer. They can be divided into those that target the immune system (checkpoint inhibitors) and those that target oncogenic membrane receptors (HER2) or other surface molecules of unknown function (CD20). Trastuzumab is a standard component of the treatment of HER2-positive breast cancer. Its development in the 1990s was considered a landmark achievement in the field of targeted therapy. When combined with chemotherapy, it improves progression-free survival (PFS) and OS in metastatic HER2-positive breast cancer and DFS and OS in early-stage HER2-positive breast cancer. These conclusions have been consistently proven by multiple phase III clinical trials in the metastatic and adjuvant settings.[90-95] First generation of small-molecule tyrosine kinase inhibitors (TKIs) were not found effective in the adjuvant setting, whereas second-generation TKIs had modest activity in the adjuvant setting (see below). The failure of TKIs to make a significant difference in the outcomes of these patients suggests that blocking the oncogenic stimulation of HER2 might not be the main mechanism of action of HER2-targeting MAbs.

Indeed, trastuzumab’s mechanism of action remains elusive. It targets HER2 and leads to its internalization and degradation. It inhibits downstream signaling pathways leading to decreased proliferation and increased apoptosis of cancer cells. Recently, its role in activating the immune system against tumor cells emerged as the main mechanism of action. The FinHer investigators found that every 10% increase in TILs was associated with decreased distant recurrence[2] and other studies found that TILs had a prognostic and predictive value as their presence predicted for higher pCR to trastuzumab-containing chemotherapy and better DFS.[19,96] A meta-analysis of neoadjuvant RCTs showed that the pCR rate was significantly higher in patients with lymphocyte-predominant breast cancer in HER2-positive breast cancer settings, with an absolute difference of 33.3% (95% CI = 23.6%-42.7%).[97]

The nature of tumor-infiltrating immune cells is more important than the mere presence or absence of TILs. Using CIBERSORT (leukocyte gene matrix LM22) to characterize immune cell composition of 7270 unrelated breast cancer samples from their gene expression profiles, Bense et al showed that the composition of the immune cell types differed per breast cancer subtype and interacted with the treatment. Increased fraction of Treg cells in HER2-positive tumors was associated with a lower pCR rate (odds ratio [OR] = 0.15) as well as shorter DFS (HR = 3.13) and OS (HR = 7.69). Increased fraction of γδT cells in all patients with breast cancer was associated with a higher pCR rate (OR = 1.55), prolonged DFS (HR = 0.68) and, in HER2-positive tumors, with prolonged OS (HR = 0.27). A higher fraction of activated mast cells was associated with worse DFS (HR = 5.85) and OS (HR = 5.33) in HER2-positive tumors. Furthermore, a high CD8+ T-cell exhaustion signature score was associated with shortened DFS in patients with ER-positive tumors regardless of HER2 status (HR = 1.80).[98]

The implications of these findings are substantial. Sorting out the antioncogenic from the immune stimulating roles of trastuzumab may be very difficult. However, the available data from the ALTTO (Adjuvant Lapatinib and/or Trastuzumab Treatment Optimization) study suggest that interrupting HER2 downstream signaling using lapatinib does not add any benefit in early-stage breast cancer.[99] The role of extended HER2 inhibition with neratinib, a second-generation HER2-targeting TKI, after completing trastuzumab therapy in the patients with HER2-positive breast cancer was tested in the ExteNET trial. This trial showed a modest benefit of 2% improvement in invasive DFS leading the Food and Drug Administration (FDA) to approve the drug.[100] It is not clear whether all TKIs will behave like lapatinib and neratinib. The challenge for future development of novel drugs is to capitalize on the immune mechanism.

Antibody-drug conjugates

Antibody-drug conjugates are MAbs targeting a cancer-specific antigen and are linked to a payload of a cytotoxic drug by a linker.[101] Antibody-drug conjugates are stable in the systemic circulation and most of the drugs in use to date have cleavable linkers that, after enzymatic cleavage or the exposure to a reduced pH (potential of hydrogen) or reduction by cytosolic thiols, release the cytotoxic drug inside the antigen-expressing cells.[102] Antibody-drug conjugates using noncleavable linkers require a thorough catabolism in the lysosomes leading to the release of their cytotoxic drug that should exit the lysosome to cause cell death. The example of the latter is TDM1. The most commonly used payloads target either tubulins or DNA. TDM1 employs DM1, a strong microtubule inhibitor of the maytansinoid class. The selection of the surface targets depends on their high expression on cancer cells and low or no expression on normal cells. Rapid internalization of the ADCs after antibody binding is a prerequisite to their activity.

TDM1 or ado-trastuzumab emtansine is now FDA approved for patients with HER2-positive MBC whose disease has progressed on trastuzumab and a taxane based on the results of the EMILIA (emtansine versus capecitabine plus lapatinib in patients with previously treated HER2-positive advanced breast cancer) trial. The trial randomly assigned the 991 patients enrolled in the study to capecitabine and lapatinib (control, n = 496) or trastuzumab emtansine (n = 495). The study had 2 coprimary end points: PFS and OS. Both end points were reached and were statistically superior in patients receiving ado-trastuzumab emtansine (difference in PFS medians of 3.2 months, HR = 0.65 [95% CI = 0.55-0.77], P < .0001 and difference in OS medians of 5.8 months, HR = 0.68 [95% CI = 0.55-0.85], P = .0006).[103] Thrombocytopenia (14%), increased aspartate aminotransferase (5%), and anemia (4%) were the most frequently reported grade 3 adverse events on the TDM1 arm and diarrhea (21%) followed by palmar-plantar erythrodysesthesia syndrome (18%) in the control arm. Despite the success of TDM1 in HER2-positive breast cancer, 50% of the patients did not respond on the EMILIA trial. To meet the need of those patients, other ADCs targeting HER2 are being investigated. Three ADCs targeting HER2 are using trastuzumab, DS-8201a (drug/target: exatecan/topoisomerase I), SYD985 (drug/target: duocarmycin/DNA), and ADCT-502 (drug/target: pyrrolobenzodiazepine dimer/DNA). The other ADCs targeting HER2 are using different MAbs and different drugs and targets.[102] Three ADCs are being developed for TNBC (Table 1).

Table 1.

ADCs in development for triple-negative breast cancer.

Name	ADC target	Drug class/target	Latest development stage	Sponsor/trial ID
Sacituzumab govitecan IMMU-132	Trophoblast cell surface antigen 2 (TROP2)	Irinotecan/topoisomerase I	Metastatic TNBCPhase III	Immunomedics NCT02574455
Glembatumumab vedotin CDX-011 CR011-vc-MMAE	Glycoprotein nonmetastatic b (GPNMB)	Auristatin/tubulin	Metastatic TNBCPhase II	Celldex Therapeutics NCT01997333
SAR566658 anti-CA6-DM4	CA6 sialoglycotope of MUC1	Maytansinoid/tubulin	Metastatic TNBCPhase II	Sanofi NCT02984683

Abbreviations: ADC, antibody-drug conjugate; TNBC, triple-negative breast cancer.

Checkpoint inhibitors

Targeting programmed death-1 and programmed death-ligand 1 (PD-1/PD-L1) in breast cancer appears increasingly appealing after the success of such an approach in other cancers. The PD-1 receptor inhibits innate and adaptive immunity when upregulated on immune cells and engaged by its ligand, PD-L1.[104] Cancers take advantage of this mechanism to induce a local immunosuppression by overexpressing PD-L1. The prognostic significance of PD-L1 is still unclear, as some studies have described its value as a positive and other as negative prognostic factor.[105,106] Regardless, the inhibition of the PD-1/PD-L1 pathway is based on the idea of “inhibiting the inhibition” of the immune system. The agents being tried in breast cancer draw from those already being used in melanoma and other malignancies including nivolumab and pembrolizumab (anti-PD-1 antibodies) and atezolizumab (PD-L1 inhibitor). Currently, results from a phase Ib study in heavily pretreated patients with TNBC who received pembrolizumab demonstrated an acceptable toxicity and good safety profile.[107] The KEYNOTE-086 trial is a phase II study with pembrolizumab in patients with metastatic TNBC as first-line (cohort B; n = 52; 100% were positive for PD-L1 expression) and subsequent line therapies (cohort A; n = 170; 60% were positive for PD-L1 expression).[108,109] Overall response rate (ORR) was 4.7% in cohort A and 23% in cohort B. The 1- and 2-year OS rates were 37% and 18% in cohort A and 63% and 47% in cohort B, respectively. Similar results for ORR were obtained using single-agent atezolizumab in frontline (first line 23%) and subsequent line settings (second line 4% and third line 8%).[110]

Combinations of checkpoint inhibitors with chemotherapy were found to be promising in preclinical studies. The combination of pembrolizumab and eribulin was tested in a phase Ib/II study in 39 patients with TNBC, half of them were chemo-naïve and 43.6% were PD-L1 positive.[111] Overall response rate with the combination was 33.3% (95% CI = 19.5%-48.1%). The CR rate was 2.6%. Stable disease for ⩾8 weeks was seen in 28.2% of patients. KEYNOTE-355, a phase III trial is underway to explore the safety and efficacy of pembrolizumab plus chemotherapy as first-line therapy in 858 patients with locally recurrent inoperable or metastatic TNBC (NCT02819518).[112] The combination of atezolizumab and nab-paclitaxel in first-line metastatic TNBC showed an ORR at 46% with 8% of patients achieving complete response.[113] Based on the results of this study, a phase III trial was launched (NCT02425891).[114] When pembrolizumab was added to standard neoadjuvant chemotherapy using anthracycline and paclitaxel, it increased pCR rates from 20% (15/21) in the control arm to 71% (16/83) in the pembrolizumab arm in a group of patients with TNBC.[111]

More trials using PD-1/PD-L1 inhibitors are being planned in TNBC as this is the breast cancer subtype in which PD-1+ TILs and PD-L1+ cancer cells are more commonly seen.[115] A randomized, phase III trial to evaluate the efficacy and safety of pembrolizumab as adjuvant therapy for TNBC with ⩾1 cm residual invasive cancer or positive lymph nodes (ypN+) after neoadjuvant chemotherapy started accruing patients in November 2016.[116]

CTLA-4 is another immune checkpoint that is being targeted in breast cancer. Similar to the PD-1/PD-L1 inhibitors, most ongoing clinical trials involving CTLA-4 generally revolve around melanoma. Ipilimumab is a CTLA-4 MAb FDA approved for the treatment of unresectable melanoma.[117] It is currently being used in a phase I study examining its safety in combination with a new anti-B7-H3 mAb, enoblituzumab, to patients with multiple refractory cancers, including TNBC.[118] Ipilimumab is also being combined with entinostat and nivolumab in a phase I study for metastatic HER2-negative breast cancer as well as with just nivolumab in a phase II study for patients with recurrent stage IV HER2-negative breast cancer.[119] There are other ongoing trials evaluating the combination of a CTLA-4 inhibitor, with additional treatments. There is a phase II study of tremelimumab (CTLA-4 inhibitor) with a PD-L1 inhibitor, MEDI4736, in patients with HER2-negative breast cancer to look for the safety and efficacy of this regimen.[120] A phase I study has already been completed with the combination of tremelimumab and exemestane in patients with hormone-responsive advanced breast cancer.[121] Besides demonstrating that this treatment regimen is tolerable, the study showed that there was an associated increase in T cells with inducible costimulators (ICOS) and that more of the patients with stable disease tended to express higher levels of ICOS+ T cells versus the patients with progressive disease.[121] CTLA-4 inhibitors have been evaluated in combination with other interventions as well. A phase I trial evaluating preoperative intervention in the form of ipilimumab and/or cryoablation in early-stage breast cancer showed these treatments to be safe and tolerable and plans are being made for a phase II trial with this regimen.[122]

Future development of these treatments should balance their benefit with their potential toxicity. CTLA-4 mAbs have been shown to have immune-related adverse events mostly affecting the skin and gastrointestinal tract.[117] Other toxicities include hepatitis, thyroiditis, colitis, and hypophysitis.[123] Compared with treatments targeting CTLA-4, therapies targeting PD-1/PD-L1 appear to have a lower frequency of immune-related adverse events.[124] The combinations of anti-PD-1/PD-L1 mAbs and anti-CTLA-4 mAbs are more effective than single agents but they may be associated with increased incidence of pneumonitis that responds to holding the drug and/or using immunosuppressive agents; the rate of pneumonitis was 5% in one study.[125]

Lymphocyte activation gene-3 (LAG-3) is expressed on activated T cells, NK cells, and DCs and has more affinity for the MHC-II than CD4. It suppresses activation and proliferation of these cells allowing the immune reaction to wind down. IMP321 is a soluble form of LAG-3. It prevents the inhibition of LAG-3–bearing cells. It was evaluated in combination with paclitaxel in patients with MBC in a phase I/II trial. Overall response rate was 50% and clinical benefit was 90% at 6 months.[126] A randomized phase II trial is enrolling (NCT02614833).

Stimulatory molecule agonist antibodies

The optimal immune response requires the engagement of costimulatory receptors expressed by CTLs, NK cells, CD4+T cells, or APCs. The most relevant receptors are CD27, CD28, CD40, OX40, 4-1BB, GITR, and ICOS. In addition to activating the proliferation and function of the cells carrying these receptors, their activation is associated with suppression of Tregs. The MAbs and fusion proteins were produced to target these receptors and many of them are now in phase I or II trials.[127]

MEDI6469, OX40 agonist MAb with strong stimulatory activity of T cells, is now in clinical investigation. It is being studied with stereotactic body RT in patients with breast cancer with metastatic lesions.[128]

4-1BB:4-1BBL is expressed on T cells and APCs, respectively. The engagement of the receptor by its ligand leads to stimulation of CD8+ T cells and NK cells with increased ADCC (antibody-dependent cell-mediated cytotoxicity), pro-inflammatory cytokines, and cytolytic activity.[129] Urelumab (BMS-663513), a 4-1BB agonist MAb, was found to have a synergistic effect with trastuzumab in murine xenotranplant model of human breast cancer.[130]

CD40 can be expressed on immune cells and breast cancer cells. CD40 is expressed on APCs and its ligation is necessary to increase their antigen presentation and cytokine production that are culminated by increased T-cell activation.[131] Although increased cytoplasmic expression of CD40 is the highest in hormone receptor–positive breast cancer,[132] its membrane expression is higher on TNBC cell lines such as MDA-MB 231.[133] The use of recombinant human CD40 ligand (rhCD40L) in cell culture of a TNBC cell line inhibited proliferation and synergized with the addition of interferon gamma and doxorubicin.[134] Hence, CD40 agonist antibodies may exert their antitumor effect directly by targeting cancer cells and indirectly by activating the effector arm of the immune system targeting the tumor.[131]

Combination immunotherapy trials with other therapies

The PD-1 MAbs (nivolumab and pembrolizumab) and PD-L1 MAbs (atezolizumab, durvalumab, and avelumab) are being tested in many combination clinical trials (Tables 2 and 3). Some trials are exploring combinations with chemotherapy and others with biological agents targeting HER2-positive or hormone receptor–positive breast cancers. However, most of these studies are designed for TNBC due to its known immunogenicity and results from single-agent checkpoint inhibitors that showed efficacy in this subtype. Likewise, many IO (immuno-oncology) combination trials have been designed in the neoadjuvant and adjuvant settings using different combinations of checkpoint inhibitors with other checkpoint inhibitors, with chemotherapy, cytokines, or with vaccines (Table 4).

Table 2.

Ongoing PD-1 MAb combination trials in MBC.

Study phase	Immunotherapy type	Other therapies	Breast cancer type	Clinicaltrials.org number
	PD-1
I	Nivolumab	Nab-paclitaxel ± gemcitabine or carboplatin	MBC, pancreatic cancer, and NSCLC	NCT02309177
II	Nivolumab	Cabozantinib (MET inhibitor)	TN-MBC	NCT03316586
Ib/II	Pembrolizumab	Eribulin	TN-MBC	NCT02513472
II	Pembrolizumab	Carboplatin	MBC	NCT03213041
II	Pembrolizumab	Anthracycline or endocrine therapy	HR+ and TN-MBC	NCT02648477
II	Pembrolizumab	Nab-paclitaxel	TN-MBC	NCT02752685
Expl.	Pembrolizumab	Nab-paclitaxel and carboplatin	TN-MBC	NCT03121352
II	Pembrolizumab	Eribulin	HR+ MBC	NCT03051659
II	Pembrolizumab	Cyclophosphamide	TN-MBC	NCT02768701
II	Pembrolizumab	With carboplatin versus carboplatin alone	Chest wall breast cancer	NCT03095352
II	Pembrolizumab	Capecitabine	TN-MBC	NCT03044730
Expl.	Pembrolizumab	Paclitaxel	HR+ and TN-MBC	NCT03018080
II	Pembrolizumab		IBC	NCT02411656
II	Pembrolizumab with	Vorinostat and tamoxifen	HR+ MBC	NCT02395627
II	Pembrolizumab	Chemotherapy	TNBC	NCT02734290
II	Pembrolizumab	Carboplatin and gemcitabine	TN-MBC	NCT02755272
II	Pembrolizumab	XRT	TN-MBC	NCT02730130
II	Pembrolizumab	Imprime PGG	TN-MBC and metastatic melanoma	NCT02981303
II	Pembrolizumab		BRCA-mutated MBC	NCT03025035
II	Pembrolizumab	XRT	HR+ MBC	NCT03051672
II	Pembrolizumab	Selective androgen receptor modulator (SARM) GTX-024	TN-MBC	NCT02971761
II	Pembrolizumab	Abemaciclib	HR+ MBC	NCT02779751
Ib	Pembrolizumab	TDM1	HER2+ MBC	NCT03032107
II	Pembrolizumab	BGB324	TN-MBC or LABC	NCT03184558
II	Pembrolizumab	Letrozole and palbociclib	HR+ MBC	NCT02778685
I/II	Pembrolizumab	Binimetinib	TN-MBC or LABC	NCT03106415
I	Pembrolizumab	JAK2 inhibition	TNBC	NCT03012230
II	Pembrolizumab	BGB324	TN-MBC or LABC	NCT03184558
II	Pembrolizumab	Letrozole and palbociclib	HR+ MBC	NCT02778685

Abbreviations: IBC, inflammatory breast cancer; LABC, locally advanced breast cancer; MBC, metastatic breast cancer; NSCLC, non–small-cell lung cancer; TNBC, triple-negative breast cancer; TN-MBC, triple-negative metastatic breast cancer.

Table 3.

Ongoing PD-L1 MAb combination trials in MBC.

Study phase	Immunotherapy type	Other therapies	Breast cancer type	Clinicaltrials.org number
	PD-L1
II	Atezolizumab	Cobimetinib (MEK inhibitor)	MIBC	NCT03202316
II	Atezolizumab	Carboplatin	TN-MBC	NCT03206203
IIA	Atezolizumab	Paclitaxel, trastuzumab, and pertuzumab	HER2+ MBC	NCT03125928
III	Atezolizumab	Chemotherapy	TN, recurrent LABC, or MBC	NCT03371017
Ib	Atezolizumab	TDM1 or TP	HER2+ BC	NCT02605915
II	Atezolizumab	Veliparib either alone or in combination	HDR-deficient TNBC	NCT02849496
Ib/II	Atezolizumab	With or without entinostat	TN-MBC	NCT02708680
I	Durvalumab	Hypofractionated XRT and tremelimumab	MBC, metastatic lung, melanoma, and pancreatic cancer	NCT02639026
I/II	Durvalumab	Olaparib or cediranib	TN-MBC or LABC, metastatic lung, prostate, and CRC	NCT02484404
II	Avelumab	Palbociclib and fulvestrant	HR+/HER2− MBC, after CDK and endocrine therapy (PACE)	NCT03147287

Abbreviations: CRC, colorectal cancer; LABC, locally advanced breast cancer; MBC, metastatic breast cancer; NSCLC, non–small-cell lung cancer; TNBC, triple-negative breast cancer; TN-MBC, triple-negative metastatic breast cancer.

Table 4.

Ongoing neoadjuvant and adjuvant combination immune-oncology trials in breast cancer.

Study phase	Immunotherapy type	Other therapies	Breast cancer type	Clinicaltrials.org number
	PD-1
Expl.	Pembrolizumab	Nab-paclitaxel	HR+ BC	NCT02999477
III	Pembrolizumab	CTx	TNBC	NCT03036488
III	Pembrolizumab	CTx	TNBC	NCT02819518
II	Pembrolizumab	Hormonal therapy	Adjuvant HR+	NCT02971748
II	Pembrolizumab	Decitabine	HR+/HER2−TNBC	NCT02957968
	PDL-1
II	Atezolizumab	Carboplatin and paclitaxel	TNBC	NCT02883062
Expl.	Durvalumab	Tremelimumab	HR+	NCT03132467
I/II	Durvalumab	Weekly nab-paclitaxel and ddAC	TNBC	NCT02489448
II	MPDL3280A	Nab-paclitaxel	TNBC	NCT02530489
III	Atezolizumab	Paclitaxel	TNBC	NCT03125902
III	Atezolizumab	CTx	TNBC	NCT03281954
III	Atezolizumab	Anthracycline/nab-paclitaxel	TNBC	NCT03197935
	Cytokines
Ib/II	IRX 2		Preoperative early-stage BC	NCT02950259
Expl.	Anakinra (IL-1R antagonist) +	Chemotherapy + dendritic cell vaccine	TNBC	NCT02018458
	Vaccine
I/II	Talimogene laherparepvec	CTx	TNBC	NCT02779855
I	Personalized polyepitope DNA vaccine		AdjuvantTNBC with persistent disease following neoadjuvant chemotherapy	NCT02348320
I	Personalized synthetic long-peptide breast cancer vaccine		AdjuvantTNBC with persistent disease following neoadjuvant chemotherapy	NCT02427581
II	Herceptin and the HER2 vaccine E75		AdjuvantHER2+ BC	NCT01570036
III	Pembrolizumab		AdjuvantTNBC	NCT02954874
I/II	Pembrolizumab ± XRT		TNBC	NCT02977468
II	Nivolumab	Ipilimumab	BC (also in ovarian and gastric cancer)	NCT03342417
IB	Mammaglobin-A DNA vaccine	Neoadjuvant hormonal therapy	HR+ BC	NCT02204098
Ib	PVX-410 vaccine	Alone and in combination with durvalumab	Adjuvant in stage II and III TNBC	NCT02826434
II	Nelipepimut-S + GM-CSF (NeuVax)	Trastuzumab	HER2+ BC (high risk)	NCT02297698

Abbreviation: TNBC, triple-negative breast cancer.

The immune-mediated effect of chemotherapy

Traditionally, the effect of chemotherapy has been explained by the induction of apoptosis of cancer cells after interrupting their cell cycle apparatus. However, alternative mechanisms involving the immune system have been recently invoked.[135,136] Taxanes, doxorubicin, and cyclophosphamide, which are standard chemotherapeutic agents in the treatment of breast cancer, are known to have major effects on the immune system in animals and human experiments.[136-141] For example, taxanes, as a class, increase serum IFN-γ, IL-2, IL-6, and GM-CSF levels as well as reducing the levels of IL-1 and TNF-α.[142] Paclitaxel given neoadjuvantly increases the levels of TILs within the tumor itself.[143]

The immune effects of chemotherapy may be summarized by (1) rendering dying cancer cells more visible to the immune system by exposing their TAAs, (2) stimulating the innate immune system, (3) stimulating T-cell differentiation, (4) promoting a cytokine profile that increases the likelihood of TH1 polarization, (5) inhibition of MDSCs and M2 macrophages, and (6) suppression of FOXP3+ Treg cells.[141] Acknowledging these mechanisms is of major importance to optimize their benefit and minimize toxicity to the immune system that becomes an important executioner of chemotherapy effect. Furthermore, integrating chemotherapy with vaccines or checkpoint inhibitors is promising.[144,145]

Conclusions and Future Directions

Immunogenicity of breast cancer is subtype dependent with a spectrum that spans from the most immunogenic to the nonimmunogenic subtypes. On one hand, TNBC is the most immunogenic with high mutation and neoantigen load and high MHC-I expression. The immune system is already activated against the cancer as attested by the high TILs, but the cancer is counterattacking by creating an immune suppressive environment (Tregs, MDSCs) or expressing checkpoint immune inhibitory molecules (CTLA-4, PD-1/PD-L1). On the other hand, luminal A is the least immunogenic with the lowest mutation and neoantigen load and the loss or downregulation of the expression of TAAs. MHC-I expression is significantly reduced or absent. Hence, infiltration with TILs is minimal if any. High local concentrations of estrogen stimulate growth and maintain a local immune suppression by attracting Tregs and MDSCs. The other breast cancer subtypes fall in between these 2 extremes.

The overall goal of cancer immunotherapy is the activation of the immune system against the cancer. Vaccination has traditionally been to boost the latent immune response to tumor-specific antigens. Approaches have included cell-based protocols involving immunization with whole autologous or allogeneic tumors, as well as antigen-based strategies involving immunization with proteins or peptides overexpressed in tumors and underexpressed in normal tissues. HER2 and MUC1 are the predominant antigens used in human breast cancer vaccine trials. Although vaccination using these antigens may demonstrate tumor-reducing effects, neither antigen provides any tissue or tumor specificity because both are expressed in a variety of normal tissues and tumors raising concerns about the possibility of off target damage if a robust immune response is developed. However, despite the lack of inherent tissue specificity of HER2 and MUC1, these concerns about systemic autoimmune sequelae have not been substantiated so far. Tumor-associated carbohydrate antigens are pan-immunogens that elicit responses to several antigens, thus achieving the same goal as a multivalent vaccine. To overcome their low immunogenicity, investigators have used CMPs that seem to elicit a broad-spectrum antitumor reactivity. Here again, the activation of immune responses against TACAs raises concerns regarding the balance between “tumor destruction” and “tissue damage,” as TACAs are also expressed on normal tissues. The evidence gleaned from phase I and II trials is reassuring. It is not clear which subtype of breast cancer would benefit from this approach.

Monoclonal antibodies are an integral part of our armamentarium in the fight against cancer. They can be divided into those that target the immune system and those that target oncogenic membrane receptors (HER2) or other surface molecules of unknown function (CD20). Anti-HER2 antibodies have changed the outlook of this disease. The failure of small molecules that inhibit the oncogenic stimulation of HER2 and the lack or minimal response to these antibodies in tumors that lack TILs suggest that their action is more immune mediated than oncogenic mediated.

Monoclonal antibodies that inhibit checkpoints (checkpoint inhibitors) are changing the paradigm of care in many solid tumors. The first results of their use in breast cancer suggest that they are the most effective in TNBC. Their use is being investigated in the other subtypes. Due to the low immunogenicity of luminal A and B breast cancers, a combination strategy using vaccines to stimulate the immune response followed by checkpoint inhibitors is rational but its clinical usefulness remains to be proven.

Finally, the immune mechanism of chemotherapy is being increasingly recognized. Its contribution in the total effect of chemotherapy relative to the direct cytotoxic effect is not known. Any further development of chemotherapy in the future should take this aspect into consideration to maximize the immune stimulatory effect and minimize the immune suppressive effect of chemotherapy.