Tamoxifen in early-stage estrogen receptor-positive breast cancer: overview of clinical use and molecular biomarkers for patient selection

Abstract

Tamoxifen was the first targeted anticancer agent for breast cancer patients and its effects on reduction of breast cancer events and improvement in overall survival are undisputed. Hence, it has long been considered an essential part of patient care. Recent results of several large adjuvant hormonal trials evaluating the use of aromatase inhibitors in comparison with the previous standard of five years of tamoxifen has led to a paradigm shift, ensuring the inclusion of an aromatase inhibitor as part of standard endocrine therapy for most postmenopausal women diagnosed today with estrogen receptor-positive breast cancer. However, one could argue that despite statistically significant improvements in breast cancer events, an overall survival advantage has not been clear. In this review, we discuss recent genomic and molecular data pertaining to estrogen receptor-positive breast cancer and how this knowledge may aid clinicians to prescribe adjuvant hormonal treatment in the future. A combination of gene expression and genetic aberration markers may be most useful in discerning a population that is still appropriate for adjuvant tamoxifen treatment.

Keywords:

• tamoxifen
• aromatase inhibitors
• resistance
• prediction
• mutation
• endocrine therapy
• PI3K

Introduction

Hormonal therapy is considered an essential part of the management of patients with estrogen receptor (ER)-positive breast cancer. Immunohistochemically confirmed presence of ER is the most important factor that predicts response to hormonal manipulation.

The ER is a transcription factor of the nuclear receptor family, and has two isoforms, ERα and ERβ. Estradiol (E2) binding to ER induces a change in conformation which releases it from an inhibitory complex and induces dimerization.¹ Regulatory proteins may act as either coactivators or corepressors to modulate the action of ER. Coactivator proteins increase transcriptional activity of DNA elements known as estrogen response elements, and result in cell survival and proliferation.² ER may also interact with transcription factors including Fos/Jun and modulate the activity of cyclin D1, and thus impact transcription of genes that do not have estrogen response elements. These “genomic” mechanisms are referred to as nuclear-initiated steroid signaling.

About 5%–10% of endogenous cellular ERα is located near the cytoplasmic membrane.³ Membrane ERs can activate surface receptors (eg, EGFR, HER2, IGF-1R) or G protein-coupled receptors which then signal via classic transduction pathways including PI3K/Akt/mTOR and Ras/Raf/MEK/ERK.⁴ This results in activation of several kinases and phosphatases, generation of second messengers, and calcium flux. This distinct “nongenomic” signaling action occurs within seconds to minutes, and is known as membrane-initiated steroid signaling.

Endocrine therapies that either interrupt the synthesis of estrogens or interfere with estrogen-mediated signaling pathways have become an integral part of the management of hormone-dependent breast cancer. The most commonly used agent of this class is tamoxifen, a selective ER modulator. This review will focus on the current evidence, particularly for the use of tamoxifen, but also other hormonal drugs in ER-positive breast cancer. It will also discuss some recent biologic and genomic knowledge that could provide a mechanistic insight and may aid clinicians better identify those ER-positive breast cancer patients who could do well with tamoxifen treatment in the near future.

Tamoxifen

Tamoxifen is the most widely used hormonal treatment for breast cancer in both pre- and postmenopausal women. Adjuvant therapy with tamoxifen for five years resulted in a significant reduction in the annual breast cancer death rate of 34%, with an absolute reduction in mortality of 9.2% at 15 years.⁵

The antitumor effects of tamoxifen are thought to be due to its antiestrogenic activity, mediated by competitive inhibition of estrogen binding to ER.⁶ As a consequence, tamoxifen inhibits the expression of estrogen-regulated genes, including growth factors and angiogenic factors secreted by the tumor that may stimulate growth by autocrine or paracrine mechanisms.⁷ The net result is a block in the G1 phase of the cell cycle and a slowing of cell proliferation. Tumors may then regress because of this altered balance between cell proliferation and ongoing cell loss. Tamoxifen may also directly induce programmed cell death.⁸

De novo or acquired resistance may occur after treatment, limiting the effectiveness of tamoxifen in many patients. In at least some patients, the disease progresses during treatment because tumor growth can be stimulated by tamoxifen itself.⁹ Tamoxifen-stimulated growth explains the “withdrawal response” that occurs in some patients when the drug is stopped because of tumor progression, and it explains the lack of response to oophorectomy in premenopausal women if tamoxifen is not discontinued at the time tumor progression is observed.¹⁰ Possible mechanisms of tamoxifen resistance include the presence of variant ER, the absence or loss of ER, altered expression of receptor-interacting proteins, and “cross-talk” amongst ER and other growth-factor signalling pathways.^6,9,10

Some tumors spontaneously become hormone-independent despite the presence of ER; in others, tumors that are initially ER-positive become ER-negative over time.^11,12 At least two-thirds of the tumors that become resistant to tamoxifen continue to express ER, and many of these tumors regress when second-line hormonal therapy is initiated.

Aromatase inhibitors

The long-term success of tamoxifen therapy has led to the development of other endocrine approaches. Because the major source of estrogen in postmenopausal women is aromatase-mediated conversion of circulating androstenedione to estrone in peripheral tissues, an alternate approach to the management of postmenopausal breast cancer has been through the use of aromatase inhibitors.

There are two distinct mechanisms by which aromatase inhibitors block the action of aromatase and reduce local and peripheral estrogen production in postmenopausal women.¹³ Type 1 inhibitors (exemestane) have androgen-like structures that bind irreversibly to the substrate complex, permanently inactivating aromatase and leading to prolonged estrogen deprivation. Type 2 inhibitors (letrozole and anastrozole) are nonsteroidal compounds that reversibly bind to the heme component of the aromatase enzyme. The clinical significance of these differences, if any, remains to be determined.¹⁴ They almost completely suppress aromatase activity (by 97%–99%) in postmenopausal women.

Hormone-sensitive breast cancer treated with aromatase inhibitors can also acquire endocrine resistance. In theory, an inefficient inhibition of the aromatase, either due to reduced drug levels or mutations/overexpression of the enzyme, may be implicated. Site-directed mutation can indeed produce aromatase that is resistant to inhibition by some, but not all, aromatase inhibitors.^15,16 Nonetheless, clinical data show that changing the aromatase inhibitor class at disease progression (ie, from Type I to Type II, and vice versa) yields some clinical benefits, thus suggesting that inefficient inhibition of aromatase may drive some cases of disease progression. Exposure to long-term estrogen deprivation and subsequent development of acquired resistance may be accompanied by adaptive increases in ER gene expression and intercellular signalling, resulting in hypersensitivity to low estradiol levels.^17,18 Furthermore, there is evidence of increased cross-talk between the various growth factor-receptor signalling pathways and ER at the time of relapse, with ER becoming activated and supersensitized by several different intracellular kinases.¹⁶ It would seem that, following failure of aromatase inhibitors, the ER remains an integral part of the pathway sustaining tumor proliferation.

Further treatment with antiestrogen agents after development of acquired resistance to aromatase inhibitors is generally accepted. Because mechanisms of acquired resistance to tamoxifen are thought to be similar to those developing after exposure to aromatase inhibitors, tamoxifen does not appear to be an ideal candidate to treat tumors regrowing after aromatase inhibitor exposure. In such an environment tamoxifen may mainly act as an agonist.¹⁶ However, recent results of the BIG 1–98 trial do not support a significant detrimental clinical effect of prescribing tamoxifen after letrozole, as previously hypothesized.¹⁹

Fulvestrant

The search for an antiestrogen devoid of the agonist activity of tamoxifen and which can effectively block ER activity resulted in the discovery and clinical development of fulvestrant.^20,21

Fulvestrant is a pure ER antagonist, without known agonistic properties, that downregulates cellular levels of the ER in a dose-dependent manner.^22–24 It binds to the ER but, due to its steroidal structure and long side chain, induces a different conformational shape with the receptor to that achieved by the nonsteroidal antiestrogen, tamoxifen. As a result, fulvestrant prevents ER dimerization and leads to the rapid degradation of the fulvestrant-ER complex, producing the loss (down-regulation) of cellular ER.²⁵ Fulvestrant, unlike tamoxifen, inhibits ER-DNA binding and produces abrogation of estrogen-sensitive gene transcription.²⁶ In vitro, fulvestrant significantly inhibits the expression of genes such as c-myb and c-myc in cells resistant to long-term estrogen deprivation, and may therefore be an appropriate therapeutic option after progression on aromatase inhibitors.¹⁷ Unfortunately clinical development of fulvestrant has been hampered by poor oral bioavailability, with the intramuscular route of administration plagued by solubility and dosage problems, and confusing clinical results. Despite the encouraging preclinical data, clinical data showed only equivalence to aromatase inhibitors and tamoxifen.²⁷ It currently seems that the true potential of this hormonal agent may never be fully realized.

Adjuvant hormonal trials

In general, the studies that have included aromatase inhibitors in the treatment of postmenopausal women with early breast cancer have evaluated their use in three distinct ways, ie, as front-line adjuvant therapy for five years in substitution of tamoxifen (up-fronting approach), as sequential adjuvant therapy following 2–3 years of tamoxifen for 3–2 years up to a total duration of five years (switching approach), or as additional five years after completion of five years of tamoxifen (extending approach).^28,29

The ATAC trial compared five years of upfront anastrozole with five years of tamoxifen, or the combination of both.^29,30 The combination arm showed no added benefit over the tamoxifen arm, and it was closed. A peak in recurrence at two years was observed in patients receiving tamoxifen, but not in those receiving anastrozole. At a median 100-month follow-up, disease-free survival was significantly improved in patients treated with anastrozole. No significant difference in overall survival was observed (see Table 1).

Table 1 Summary of currently reported adjuvant hormonal therapy trials. Overall, compared with five years of tamoxifen alone, the incorporation of an aromatase inhibitor significantly improves disease-free survival

Study	Patients (N)	Last follow-up (months)	AI	Comparator	DFS HR	Pvalue	OS HR	Pvalue	REF
Up-front adjuvant
ATAC	5216	100	ANA	TAM	0.85	0.003	0.97	0.7	29
BIG 1–98 (MA)	4922	76	LET	TAM	0.88	0.03	0.81	0.08	31
TEAM	9766	33	EXE	TAM	0.83	0.02	NR	NR	33
Switch adjuvant
IES	4724	56	EXE	TAM	0.76	0.001	0.85	0.08	34
ABCSG 8/ITA/ARNO 95	2577	84	ANA	TAM	0.59	0.0001	0.71	0.04	35
Extended adjuvant
MA.17	5187	30	LET	Placebo	0.58	0.001	0.98	0.853	36

Abbreviation: MA, monotherapy arm.

The BIG 1–98 trial randomized patients to either five years of tamoxifen, five years of letrozole, two years of tamoxifen followed by three years of letrozole, or two years of letrozole followed by three years of tamoxifen. An initial analysis, at a median follow-up of 25.8 months, demonstrated a significantly improved disease-free survival in the frontline letrozole arm.³¹ These results have also been confirmed at a more recent analysis (76-month median follow-up). However, this study did not show that either tamoxifen or letrozole initial therapy had a significant effect on overall survival. An analysis of the two sequential treatment arms (with a median follow-up of 71 months) reported¹⁹ that none of the study outcomes was significantly improved using either sequential therapy compared with letrozole monotherapy. Trends support initial use of letrozole in patients at higher risk of relapse. Patients commenced on letrozole can be switched to tamoxifen if required. Updated results of the monotherapy comparison suggest a trend towards superior overall survival with letrozole compared with tamoxifen (see Table).

The TEAM (Tamoxifen Exemestane Adjuvant Multinational) trial compared upfront tamoxifen with upfront exemestane. An initial analysis at 2.75 years showed a nonsignificant trend in disease-free survival benefit, indicating an improved outcome with exemestane versus tamoxifen in the intent to treat population.³² Excluding patients who have never received a study drug, disease-free survival significantly improved with exemestane. At a median follow-up of 5.1 years, exemestane monotherapy and sequential therapy achieved similar disease-free survival and overall survival (see Table).³³

The IES study compared a switch to exemestane or continued tamoxifen after an initial 2–3 years of tamoxifen therapy, for a total of five years. An eight-year follow-up showed the switch significantly improved both disease-free survival and overall survival (see Table).³⁴

A meta-analysis of three trials (ABCGS-8, ITA, ARNO) comparing five years of tamoxifen with tamoxifen followed by anastrozole showed a significantly improved disease-free survival and overall survival in patients in the switching arms.³⁵

The MA.17 study randomized patients who had completed 4.5–6.0 years of tamoxifen to either five years of subsequent letrozole therapy or placebo.^36,37 At a median follow-up of 2.5 years, patients who continued adjuvant treatment with letrozole experienced significantly improved disease-free survival, but no change in overall survival (see Table). However, a retrospective subgroup analysis revealed a significant benefit in overall survival among patients with node-positive disease.

Genomic contribution to definition of tamoxifen-sensitive breast cancer

Current guidelines recommend the inclusion of adjuvant endocrine therapy in almost all patients whose tumors show evidence of endocrine responsiveness.³⁸ However, the heterogeneity of breast cancer, clinical behavior, and response to endocrine treatment has long been apparent to clinicians, despite positive expression of ER and its related genes, and in the adjuvant setting up to 30% of patients with ER-positive breast cancer relapse despite the treatment due to either intrinsic or acquired resistance.⁵

Given the heterogeneity and complexity of breast cancer disease, it is probably unlikely that one predictive biomarker can capture and explain the differences in clinical outcome for all ER-positive tumors. For this reason, in recent years, whole genome microarray and other high-throughput technologies able to provide simultaneous characterization of thousands of genes have been extensively used in an attempt to define more accurate prognostic and predictive markers for breast cancer, and to obtain a mechanistic insight into the reasons underlying sensitivity and resistance to tamoxifen treatment.

Molecular classification of breast cancer and prognostic implications

Unsupervised hierarchic clustering analysis has identified multiple molecular subgroups within breast cancer. The most commonly cited microarray classification divides breast cancers into four main groups: the “basal-like” subtype, which is predominantly ER-negative, PR-negative, and HER2-negative; the HER2-like subtype, characterized by increased expression of genes located in the HER2 amplicon; and at least two “luminal-like” subtypes, predominately ER-positive, named luminal A and B.^39–42 Interestingly, these molecular phenotypes were associated with distinct clinical outcomes. When originally described, the luminal A subgroup had the highest expression of ER and ER-regulated genes and a better clinical outcome compared with the luminal B subgroup, suggesting an underlying molecular basis of the heterogeneity of clinical outcome in breast cancer. Relevant to this review article, a group of ER-positive cancers that had an unfavorable outcome even when treated with adjuvant endocrine treatment could be observed.⁴⁰ These data heralded much early excitement and reinforced to clinicians and scientists alike that breast cancer subtypes were likely to need different therapeutics and that the biology of disease progression was probably unique for each subgroup. Unfortunately, despite these seminal publications, clinically implemented stratification of luminal A and B subtypes is currently rare.

Several predictive gene sets and assays have been developed over recent times to aid clinicians identify those ER-positive breast cancers that have a poor clinical outcome despite tamoxifen treatment in the hope of determining which patients may be suitable for tamoxifen, either alone or sequentially, and those with a poor prognosis who may require chemotherapy, aromatase inhibitors, or other targeted strategies.^43–47 One of the most successful assays was developed by Genomic Health using quantitative real-time polymerase chain reaction and was derived by analyzing the results from three preliminary studies involving 447 samples from a heterogeneously treated population (chemotherapy and tamoxifen) and 250 candidate genes selected after a literature search of the most important microarray experiments relating to breast cancer prognosis.⁴³ Of these, 21 genes were chosen, five of which were control genes; the derived multigene predictor assigned a “recurrence score” to predict low-, intermediate-, and high-risk of distant recurrence for women receiving five years of adjuvant tamoxifen (± chemotherapy).

The predictor was subsequently validated prospectively in archival patients who had received tamoxifen only in the NSABP B-14 trial. The recurrence score accurately predicted patients at high-risk versus low-risk of recurrence on tamoxifen, identifying those who do poorly with tamoxifen treatment. The recurrence score is currently the subject of a global Phase III randomized trial evaluating its ability to select ER-positive breast cancer patients for either adjuvant hormonal treatment alone or with standard chemotherapy.

The gene expression grade index (GGI) score is based on 97 genes found to be consistently differentially expressed between low (Grade 1) and high (Grade 3) histologic grade breast cancer.⁴⁹ Not surprisingly, these genes are mainly involved in cell cycle regulation, proliferation, apoptosis evasion, and differentiation. Of note, the GGI was shown to be able to define two distinct molecular subgroups within ER-positive breast cancer that were highly comparable with the previously defined luminal A and B classification. The samples previously classified as luminal A or B were associated with significantly different GGI values, with luminal A subtypes being associated with low GGI values and the luminal B tumors having significantly higher GGI values. Of note, these two subtypes were associated with statistically distinct outcomes in both systematically untreated and tamoxifen-treated populations.^47,49 These studies were important because they reinforced the hypothesis that the proliferative phenotype is associated with a poor prognosis in ER-positive breast cancer, thus highlighting a group not suitable for tamoxifen monotherapy and a group with a critical need for further research. The molecular “drivers” of the luminal B or highly proliferative ER-positive phenotype, and what may be its best therapeutic strategy remain to be determined. It is probable that a few molecular targets will emerge, such as PIK3CA and FGFR1 amplification. As such, it is currently far from clear if aromatase inhibitors, fulvestrant, or chemotherapy can change the natural disease history of this subgroup. Future integrative genomic and deep sequencing studies may shed further biologic light for these breast cancer patients in the future. However, it is imperative that clinical trials prospectively stratify for luminal prognostic subtypes using some measure of tumor proliferation activity. Markers such as Ki67 immunohistochemistry, histologic grade, GGI, or recurrence score may be useful in this regard.

Gene expression predictors of response to endocrine treatment

While molecular profiling of breast cancer has shown the existence of different prognostic tumor phenotypes within the ER-positive population, determining if any of these gene signatures could act as a predictive biomarker of benefit from endocrine agents rather that just prognosis (ie, independent of treatment) has been more difficult. Many of the aforementioned studies involved tumors that had been treated with tamoxifen, but a poor prognosis may be related to inherent tumor aggressiveness as well as tamoxifen resistance.

The recurrence score has been reported to be predictive of tamoxifen response. In particular, a low recurrence score is considered predictive of tamoxifen benefit in ER-positive, node-negative cases, while a high recurrence score is predictive of chemotherapy benefit over hormonal therapy in ER-positive patients, regardless of lymph node status.^48,50,51

In the recent past, several other gene expression signatures have been developed in an attempt to predict sensitivity or resistance to both tamoxifen and aromatase inhibitors.^52–55 In a recent study, Symmans et al⁵² hypothesizing that measurement of gene expression related to ER within a breast cancer sample represents intrinsic tumor sensitivity to adjuvant endocrine therapy, were able to define a genomic index for sensitivity to endocrine therapy (SET index) from genes coexpressed with the ESR1 gene in 437 microarray profiles from newly diagnosed breast cancer, unrelated to treatment or outcome. The association of the SET index and ESR1 levels with distant relapse risk was evaluated from microarrays of ER-positive breast cancer in two cohorts who received five years of tamoxifen alone as adjuvant endocrine therapy, a cohort who received neoadjuvant chemotherapy followed by tamoxifen and/or aromatase inhibitor, and two cohorts who received no adjuvant systemic therapy. The SET index (165 genes) was significantly associated with distant relapse or death risk in both tamoxifen-treated cohorts and in the chemoendocrine-treated cohort independent of the pathologic response to chemotherapy, but was not prognostic in two untreated cohorts. No distant relapse or death was observed after tamoxifen alone if node-negative and high SET, or after chemoendocrine therapy if intermediate or high SET. The SET index was found to be useful in estimating distant relapse-free survival if patients were to receive adjuvant endocrine therapy alone and in conjunction with other clinicopathologic information to determine whether or not additional treatment might be indicated to improve the likelihood of cure further.⁵²

Kok et al^45,56 evaluated if their 78-gene signature that was developed from a dataset of metastatic breast cancer patients who did and did not respond to tamoxifen treatment was truly predictive of tamoxifen response. They found that their signature seemed to be more predictive than prognostic compared with the recurrence score in an independent set of tamoxifen-treated ER-positive metastatic breast cancer patients. Whilst the metastatic setting may be the most logical way to investigate the true predictive ability of a biomarker, it remains plausible that metastatic breast cancer patients have different disease biology compared with those having early-stage disease.

Miller et al⁵⁴ used the neoadjuvant or preoperative setting to uncover gene profiles for which baseline expression and relative change with 14 days of treatment differed between breast cancers that were clinically responsive or resistant to letrozole therapy. The advantage of the neoadjuvant setting is that it allows multiple ways of assessment of response to therapy, eg, monitoring of changes in tumor size during the first months of treatment and sequential tumor biopsies before and after neoadjuvant treatment with letrozole. Gene expression profiles were then related to clinical responses as assessed from tumor volume measurements after three months of treatment. Bioinformatic analysis identified 205 probe sets (69 baseline expression, 45 day 14 expression, and 91 changes in expression with treatment) which differentiated between clinical responders and nonresponders. Of note, the high proportion of change and day 14 variables among the total emphasizes the need to monitor the effects of therapy on gene expression as well as baseline parameters when identifying predictive markers of response to treatment.⁵⁴ This study underscores the potential of the neoadjuvant setting for high-level correlative science, but also supports the need for biologically driven hypotheses and stratification of luminal subtypes, and also highlights the difficulties of serial analyses using high-dimensional data.

Important genetic aberrations in ER-positive patients

Some key genetic aberrations have been identified in recent years that can impact ER signaling and response to endocrine therapy. These aberrations may occur at the ER and other related surface receptor level (HER1, HER2, IGFR-1, FGFR-1), signaling pathway (PI3K, MAPK) level, and transcription factor level (myc, cyclin D1). It is important to note, that luminal A and B remains terminology for a phenotype, and that understanding the molecular aberration/s that drive the phenotype is likely to be critical for better outcomes. Following are some recent findings on the molecular alterations of key genes related to the ER pathway, their luminal phenotype and their potential clinical implications.

HER2

When ER binds to tamoxifen, it undergoes a conformational change that favors the recruitment of corepressors that inhibit transcriptional activity.⁵⁷ The subset of ER-positive patients who are also HER2-positive are known to have a relatively poor response to tamoxifen. Patients whose tumors express high levels of both HER2 and the ER coactivator AIB1 (amplified in breast cancer 1) often develop tamoxifen resistance.⁵⁸ Shou et al showed that addition of tamoxifen to the MCF-7/HER2-18 cell lines which overexpress both AIB1 and HER2 in fact resulted in growth stimulation.⁵⁷

Ellis et al have reported that when neoadjuvant tamoxifen was administered, there was a significantly lower clinical response rate among patients with HER2 amplified tumors (33%) as compared with the HER2 negative ones (49%).⁵⁹ They also reported that HER2 positivity was associated with a lower suppression of Ki67, a marker of cell proliferation, in response to tamoxifen. Hence, HER2+ is one driver of the luminal-B phenotype. Given its clinical and therapeutic implications, it should always be distinguished from other ER-positive cancers, including other luminal-B type cancers.

PIK3CA

PIK3CA mutations are seen in about 26% of breast cancers, especially in ER-positive and HER2-overexpressing subtypes (www.sanger.ac.uk/perl/genetics/CGP/cosmic). These mutations are frequently located in hotspots on exons 9 (helical domain) and 20 (kinase domain).⁶⁰ The prognostic implications of this aberration are unclear, but recent data suggest it is likely that this mutation is associated with a relatively good prognosis for ER-positive, HER2-negative breast cancer.^60–63 Although the exact mechanism for this is unclear, using gene expression and protein data from around 1800 breast tumor samples, we have reported that in ER-positive and HER2-negative tumors, PIK3CA mutations were associated with relatively low mTORC1 signaling despite the presence of constitutive pathway activation, and with a good clinical outcome from single-agent tamoxifen. Increased sensitivity to tamoxifen has been also observed in PI3K mutant cell lines compared with wild-type, so this aberration may have important clinical implications.

PIK3CA and PIK3CB amplifications have been found in a minority of breast cancers.⁶⁴ Amplification of this gene may have different functional effects compared with mutation for breast cancer. A more aggressive phenotype was reported with PIK3CA amplification compared with mutation in endometrial cancer.⁶⁵

AKT1

AKT1 mutations have been found in around 4% of breast cancers and have also been shown to be tumorigenic through activation of PI3K signaling.⁶⁶ Whilst the association with tamoxifen and outcome is not known, AKT1 mutations were reported to have a gene expression profiles similar to those of PIK3CA mutants, suggesting that AKT1 mutations may also be associated with a relatively good clinical outcome from tamoxifen therapy.⁶¹ These hypotheses remain to be validated further in the clinical setting, and are highly relevant given the current intense interest in the development of PI3K pathway inhibitors.

FGFR1

Amplification of FGFR1 occurs in around 10% of breast cancers,^67,68 and amplification of FGFR1 has been associated with a poor prognosis in ER-positive breast cancer.⁶⁹ Of note, HER2 and FGFR1 amplification rarely coexist, suggesting overlapping areas of pathway activation. FGFR1 amplification has been shown to be associated with the luminal B, ER-positive phenotype with high levels of proliferation, and hence may be a realistic potential therapeutic target for this poor prognostic group given that a number of drugs exist that inhibit this molecule.⁷⁰ Additionally, FGFR1-amplified cell lines were shown to be resistant to tamoxifen, and this resistance was reversed by siRNA silencing of FGFR1. FGFR1-amplified tumors are frequently PR-negative.

Myc and cyclin D1

Musgrove et al have suggested that estrogen regulates cell growth principally via c-Myc.⁷¹ Overexpression of c-Myc and cyclin D1 occurs in 38% (range 11%–70%) and 45% (range 28%–81%) of breast cancer patients and has been associated with tamoxifen resistance.⁷² Because these genes are involved with cell cycle regulation and proliferation activity, it is plausible that these aberrations also may be drivers of the luminal B phenotype.

Limitations of current genomic predictors

Despite their promise, none of aforementioned molecular aberrations, except for HER2, or gene signatures identified thus far has been approved for routine use in the clinical setting. There are a multitude of different reasons for this, from lack of appropriate clinical validation, unclear clinical implications, technical reasons involving standardization of the assay, tissue requirement (snap-frozen), and cost.

Although gene expression profiling has given us new insights into the biology of ER-positive breast cancer, a consistent definition of clinically relevant ER-positive subgroups is lacking. A widely accepted and standard definition could significantly help research in the field. Clinical trials could then be conducted in stratified populations because important therapy effects may be diluted or missed by analyzing an unselected ER-positive population. Whilst measurement of proliferation gene expression may provide a good starting point, the cutoff between luminal A and B groups is somewhat arbitrary due to the fact there is no clear biologic bimodality and that proliferation activity is a continuum. It will also be necessary in the future to include genetic aberrations as upfront stratification due to their differing influences on clinical outcome and response to therapy. Figure 1 demonstrates how our knowledge of the key genetic aberrations involved in the pathogenesis of the luminal subtypes has become a little clearer even in the last few years.

Figure 1 Kaplan–Meier graphs of different clinical outcomes of ER-positive breast cancer patients treated with adjuvant tamoxifen monotherapy. Patient series is described in reference ⁴⁷. Previously the gene expression grade index (GGI) was used as a measure of proliferation activity to divide ER-positive breast cancer into luminal A and B phenotypes A). Further limited knowledge of important DNA aberrations has identified PIK3CA and AKT1 mutant breast cancers with a similar survival as the luminal A subgroup and HER2 and FGFR1 amplified breast cancers as the luminal B group. Hence, FGFR1 represents a candidate molecular target for some luminal B tumors B). It is likely that both gene expression and molecular aberration may define a group of women suitable for tamoxifen monotherapy in the future.

Whilst prognostic gene signatures have been consistently shown to be helpful in ER-positive breast cancers, they seem only to identify early relapses (within five years) and hence much of the biology underlying late relapse which is common in ER-positive breast cancer, and therefore prediction of it is unknown. We are also not sure to what extent gene predictors provide better prognostication than currently widely available clinicopathologic factors. A recent study reported that a four-marker surrogate immunohistochemical panel (ER, PR, HER2, and Ki67) was able to define a luminal B phenotype. This group, together with luminal/HER2-positive tumors, was found to have worse relapse-free and breast cancer-specific survival compared with luminal A tumors, both in the presence and in the absence of adjuvant systemic treatment with either tamoxifen alone or combination chemotherapy and tamoxifen.⁷³ Notably for this study, all of these “standard” markers were performed in one central laboratory, emphasizing the poor reproducibility and quantification of local immunohistochemistry. The future may become clearer with the development of truly “predictive” biomarkers for tamoxifen response and resistance, and it is expected that a better understanding of the molecular drivers of ER-positive breast cancer using new deep and integrative genomic techniques will probably emerge. Furthermore, it has become apparent that it will be important to perform these correlative studies in the context of clinical trials to understand their clinical implications more accurately.

Can we identify patients who will do well with tamoxifen alone?

In general, the aforementioned studies that have evaluated the use of aromatase inhibitors versus tamoxifen have consistently shown that adding an aromatase inhibitor during adjuvant therapy improves disease-free survival and reduces the risk of breast cancer events compared with five years of tamoxifen monotherapy (see Table 1). However, if we look at absolute percentages, the reduction in risk of recurrence associated with aromatase inhibitors compared with tamoxifen could be considered disappointing. Upfront comparisons of tamoxifen and aromatase inhibitors are the same in terms of overall survival, supporting a main reduction from local and contralateral events (ie, not life-threatening) and even provocatively implying a worse outcome for aromatase inhibitor-treated patients after relapse and increased deaths from other causes (see Table 1). Two of the six trials of sequential treatment strategies yielded statistically significant improvements in overall survival compared with tamoxifen alone, although again the absolute difference in overall survival was small. Furthermore, aromatase inhibitors are not always well tolerated and are considerably more expensive than tamoxifen.

However, breast cancer events and early recurrence are important, and given that metastatic disease is incurable, the current standard is to include an aromatase inhibitor in the adjuvant treatment of postmenopausal women.⁷⁴ Only a minority of postmenopausal women who decline or have a contraindication to an aromatase inhibitor currently receive tamoxifen alone. Because aromatase inhibitors do not suppress ovarian estrogen synthesis fully, they cannot be used for the treatment of premenopausal women.⁷⁵

Recently, Viale et al developed a risk nomogram including tumor size, tumor grade, hormone receptor status, and HER2 status, to generate a risk model that could allow categorization of breast cancer patients into three groups, with low-, intermediate-, or high-risk outcomes.⁷⁶ Low-risk patients achieved excellent outcomes regardless of the treatment type. However, as the risk of relapse increased, differences between the aromatase inhibitor-based treatments began to emerge. Therefore, there may still be a role for using five years of tamoxifen therapy for these lower-risk women.

Research in the genomic field continues to advance our understanding of the biologic basis of relapse for ER-positive breast cancer, but clinical implementation of such findings remains slow. Currently it seems that the luminal A phenotype could do quite well with tamoxifen alone for five years. This subgroup could be identified in multiple ways, using either an immunohistochemical or gene expression assay that can quantify the expression of proliferation genes in a given breast cancer. Genetic aberrations, such as HER2 and FGFR1 amplification, could also define clearly for clinicians, without relying on arbitrary, nonbiologic cutoff for the luminal B phenotype, those ER-positive patients who will do poorly with tamoxifen treatment alone.

Conclusion

Tamoxifen treatment remains highly relevant for women diagnosed with ER-positive breast cancer. It is also clear that distinct luminal phenotypes exist and should be characterized by some proliferation marker in clinical trials, given that the treatment in the future is likely to be different for each. We feel that the most significant advances in the field of predictive biomarkers and biologic understanding will only occur in the context of innovative trials that incorporate prospectively planned translational research in their design. Hence, strong and respectful collaboration between basic researchers, clinicians, and pharmaceutical companies will be required in order to accomplish the challenging objective of a “personalized” treatment for ER-positive breast cancer patients.

Disclosure

The authors report no conflicts of interest in this work.