Updates on Adjuvant Therapy for Early Stage Hormone Receptor-Positive Breast Cancer

Ludimila L. Cavalcante, MD, and Cesar A. Santa-Maria, MD


Optimization of adjuvant systemic therapy in women with early-stage hormone receptor-positive breast cancer includes the consideration of chemotherapy and ideal type and duration of anti-hormone therapy. The use of gene expression profiling as a predictive marker for determining benefit to chemotherapy has become an important consideration when recommend-
ing chemotherapy in patients with early stage hormone receptor-positive breast cancer. Recent results from
the TAILORx and MINDACT studies provide the first prospective data, designed to give more conclusive guidance on assays. Defining the optimal adjuvant anti-hormone therapy, administered after the consider-
ation of chemotherapy, is a constantly evolving field, in which factors such as menopausal status, drug type, and duration of therapy are carefully considered. New data from the MA17R study and the 2016 San Antonio Breast Cancer Symposium (SABCS) provide early evidence
that demonstrates the benefit of extending the duration of aromatase inhibitors builds on previous studies in- vestigating extended tamoxifen or sequential therapies between these 2 drug classes. Indeed, modern breast oncology care for patients with early stage hormone receptor-positive disease involves individualizing recom- mendations based on clinical presentation and genomic assays to provide optimal chemotherapy, and anti-hor- mone regimens. This manuscript will provide updates on approaches to gene expression analysis and extended aromatase inhibitors in early breast cancer, focusing on several recent presentations and publications.

AJHO. 2016;12(12):18-23

Adjuvant Chemotherapy in Hormone Receptor-Positive Disease: To Give or not to Give

Chemotherapy in Hormone Receptor-Positive Disease
Adjuvant chemotherapy for early-stage breast cancer was first described in the 1970s,1 with systemic cytotoxic chemotherapy demonstrating an improvement in survival in patients with early stage disease. Although adjuvant chemotherapy may benefit some patients, not all patients with breast cancer derive a benefit.2 Thus, the decision to prescribe adjuvant chemotherapy is a crucial one, and while certain pathologic markers can help assess the likely benefit from systemic cytotoxic therapy, genomic assays have been studied to help predict those patients most likely to benefit from treatment.3

Gene expression microarrays have been used to define specific subtypes of breast cancer.4 These include basal-like, HER2-positive, normal breast-like, and luminal epithelial categories.4 The luminal subtypes are generally associated with the estrogen receptor (ER) and progesterone receptor (PR); however, not all ER-positive tu- mors behave similarly.5 Molecular analysis of the luminal subtypes can categorize them as luminal A and B, which behave as distinct phenotypic entities, with luminal B tumors demonstrating higher histologic grade, Ki67, and an increased risk of relapse compared to luminal A tumors.4-6 Rapidly dividing cells, as compared with more indolently dividing cells, tend to be more sensitive to chemothera- py; thus, surrogate pathological markers of rapidly dividing tumors include higher histologic grade and Ki67.7 Understanding which tumors exhibit a more aggressive phenotype can help identify which are more likely to benefit from cytotoxic chemotherapy. Gene expression assays such as PAM50 can estimate these intrinsic subtypes of breast cancer and categorize them by cumulative risk of recurrence and death.f

Although PAM50 subtypes have prognostic value in breast cancer, this molecular profiling technique has not been validated as a predictive marker of response to therapy. Although there exists various gene expression assays that may hold prognostic and/ or predictive value, the two assays that have been most rigorously validated and most commonly used in practice are the Oncotype Dx and Mammaprint assays. This review will focus on recent updates of the Oncotype Dx and Mammaprint assays from recent publications, and their implications for practical use when deciding adjuvant chemotherapy for early-stage hormone receptor-positive breast cancer.
Oncotype Dx
The Oncotype Dx recurrence score (RS) is based on a 21-gene assay, which includes numerous genes involved in breast oncogenesis and proliferation. Initial retrospective studies using tissue data from NSABP B-14, which randomized ER-positive node-negative patients to 5 years of tamoxifen or no therapy, validated the RS could predict distant recurrence.9 Results from NSABP B-20, which randomized ER-positive node-negative patients to cyclo- phosphamide, methotrexate, and 5-fluorouricil, has been used to retrospectively validate the ability of Oncotype Dx to predict the magnitude of benefit from adjuvant chemotherapy using cut offs for low, intermediate, and high scores (< 18, 18-30, ≥ 31; respec- tively).3 In the clinical setting, patients with low scores typically would not be recommended chemotherapy, whereas patients  with high scores would; the challenge has been in deciding on   the benefit of chemotherapy in patient with intermediate scores. In order to address how to approach intermediate scores and prospectively validate the Oncotype Dx assay, the Trial Assigning IndividuaLized Options for Treatment (TAILORx) study was designed in node-negative patients, and the Treatment for Posi- tive Node, Endocrine Responsive Breast Cancer  (RxPONDER) study was designed in node-positive patients. The TAILORx study determined the RS in patients with node-negative ER-positive breast cancer, if they have a low score (defined as 0 to 10) patients proceed with endocrine therapy and omit chemotherapy. If they have a high score (greater than 25) patients proceed with che- motherapy followed by endocrine therapy; however, if they have  an intermediate score (11 to 25) they are randomized to receive chemotherapy or not. Results thus far have been published for patients with a low RS, and as anticipated, these patients have favorable outcomes with disease-free survival (DFS) of 93.8%  at 5 years (95% Cl, 92.4-94.9).10 The study has not yet reported out- comes on the subgroup of patients with intermediate scores. In addition, results from the RxPONDER study will provide much needed data for chemotherapy decisions regarding the node-posi- tive group. The study is designed to randomize patients with node positive ER-positive breast cancer with an RS of 25 or less to  receive chemotherapy and hormone therapy versus hormone ther- apy alone.11 While Oncotype Dx is not considered a standard of care in node-positive patients, retrospective analysis from SWOG 8814, which tested the addition of anthracycline-based chemo- therapy to tamoxifen in postmenopausal ER-positive node-posi-  tive women, found significant survival benefit of chemotherapy in tumors with a high Oncotype Dx score (> 31), but no significant benefit in those with low scores, <18.12

While the Oncotype Dx RS can provide a perspective on dis-  ease biology and chemosensitivity, studies have demonstrated that  a simple validated model based on routine pathologic markers  (ER, PR, grade, Ki67) correlates very closely with the Oncotype score.13 Indeed, other assays, such as the IHC4 have used algo- rithms based on routine pathological markers, and can strongly predict recurrence rates and may also be helpful in determining benefit from chemotherapy.14

Mammaprint is a 70-gene gene-expression assay correlated with six hallmarks of oncogenesis: evading apoptosis, self-sufficiency in
growth signals, insensitivity to anti-growth signals, limitless replica- tion, tissue invasion and metastasis, and angiogenesis.15 Mamma- print provides a raw score which classifies tumors into low- and high-risk based on distant recurrence risk at 5 and 10 years, and has been validated as prognostic.16

The MINDACT trial was a phase 3 study in patients with early breast cancer where the primary endpoint was to assess if patients with high risk based on clinical assessment (using a modified ver- sion of Adjuvant! Online) and low genomic risk (using MammaP- rint), benefited from adjuvant chemotherapy after randomization.17 Chemotherapy regimens patients received included anthracy-
cline-based chemotherapy or docetaxel with capecitabine; anthra- cycline regimens including taxanes were not used. Among the total of 6693 patients enrolled, 23% (n = 1550) had high clinical risk and low genomic risk. These patients underwent randomization to chemotherapy (n = 1497) versus no chemotherapy, of which 82% (n = 1228) were evaluable per protocol. The rate of DFS at 5 years for those who did not receive chemotherapy was 94.7% (95% CI, 92.5-96.2) and 95.9% (95% CI, 94-97.2) in those who did receive chemotherapy; a statistically non-significant 1.5 percentage point difference (HR, 0.78; 95% CI, 0.50-1.21; P = .27). Since the study met its primary endpoint, these results suggest that patients with high clinical risk and low genomic risk do not benefit from che- motherapy. Subset analysis also found this to be the case whether patients were node-negative or node-positive. Results for the low clinical risk and high genomic risk group showed a 5-year rate of survival without distant metastasis of 95.8% (95% CI, 92.9-97.6) among those who received chemotherapy, as compared with 95% (95% CI, 91.8-97) who did not receive chemotherapy (HR, 1.17; 95% CI, 0.29-2.28; P = .66). While this was not the primary objec- tive of the study, this infers that patients with low clinical risk may not require additional testing as even those with a high score did not experience a differential benefit to adjuvant chemotherapy.

There are important limitations to consider in this study which may restrict its generalizability. For instance, the study enrolled a heterogeneous population, which included 9.5% patients with HER2-positive breast cancer, and 9.6% with triple-negative breast cancer. The ER-negative cohort was too small, comprising only 11.6% of all patients, and these results cannot be extrapolated to these patients. Moreover, because the original sample size calcu- lations were based on the total number of patients, the inclusion of ER-negative patients reduces the sample size of the ER-positive cohort, which could reduce the power to interpret results. Further- more, 21% of patients had node-positive disease, limiting conclu- sions related to this subset. Therefore, these data provide evidence primarily for patients with ER-positive, node-negative disease. Clinical risk was assigned using Adjuvant! Online which does not factor in all pathological variables that contribute to risk such as PR and Ki67; indeed, it is currently offline because it is undergo- ing updates. Finally, while the main analysis found a statistically non-significant benefit of 1.5% favoring the chemotherapy arm it is important to consider that patients were administered second generation chemotherapy regimens (either anthracycline-based or docetaxel and capecitabine). The benefit of adding a taxane to
anthracycline-based regimens has been demonstrated in numerous studies, and it is unknown if third-generation regimens in patients with Mammaprint low scores with high clinical risk would have a similar rate in DFS.18
Practical Guidance of Gene Expression Platforms
Both Oncotype DX and Mammaprint are FDA approved ge- nomic assays which can be used to guide adjuvant chemotherapy treatment decisions, each with its own limitations. The design of MINDACT couches the interpretation of Mammaprint in clinical risk, and lends itself to practical application in the setting of high clinical risk. Studies investigating Oncotype DX on the other hand
are not couched in clinical risk; rather the decision to give adjuvant chemotherapy or not depends solely on the molecular platform.
The initial results of the TAILORx study, however, demonstrate that patients who have a low RS do exceedingly well and chemo- therapy can be omitted with confidence. These different setting in which the assays have been studied and developed may help guide selection of which assay to order in clinic. However, they should be ordered when their results may affect clinical decision making,
and it is important to factor in patient and tumor characteristics, as well as patient preference, on an individual level.

Adjuvant Chemotherapy in Hormone Receptor-Positive Disease: To Give or not to Give

Experience with Anti-Hormone Therapy in Early Breast Cancer
Anti-hormone drugs were the first targeted therapy in oncology and have become a cornerstone of treatment in hormone recep- tor-positive breast cancer.19 Tamoxifen, a selective ER modulator (SERM), was the first anti-hormone therapy approved for the adjuvant treatment of breast cancer.20,21 When compared to no endocrine therapy in the adjuvant setting, the use of tamoxifen for 5 years significantly reduces the risk of breast cancer recurrence.22 Following this significant breakthrough, a more potent class of anti-hormones, the aromatase inhibitors (AI), were found to be superior to tamoxifen in postmenopausal women, with improve- ments in recurrence rates.23 The natural history of hormone recep- tor-positive breast cancer demonstrates that these types of breast cancers can recur years or even decades after initial diagnosis, suggesting that extended regimens may be helpful.24 Because of the superiority of AIs and the risk of late recurrences, several adjuvant studies have also looked at sequential administration of tamoxifen and AIs in postmenopausal patients, evaluating varying sequences and duration of therapy (Table 1). Furthermore, data investigating extended regimens of tamoxifen have found an improvement in DFS and OS, leaving the question if extended AIs would have similar benefits.25,26 This review will focus on the recent publica- tion of the MA-17R and presentations of the DATA, IDEAL, and NSABP B-42 studies at the San Antonio Breast Cancer Symposium (SABCS), which investigate various approaches to extended AI therapy.27
In the MA-17R studied patients who had finished 5 years of letro- zole after having received tamoxifen (median duration of 5 years, with 68.5% of patients receiving tamoxifen for 4.5 to 5.5 years) who were randomized to receive another 5 years of letrozole versus placebo.27 This study achieved its primary endpoint as it found that extending letrozole for an additional 5 years increased the
5-year DFS rate from 91% to 95%, (HR, 0.66, 95% CI, 0.48-0.91;
P = .01).27 The majority of the benefit observed was in preventing ipsilateral loco-regional or contralateral breast cancer recurrence with the extension of letrozole versus placebo (3.3% versus 6.4%, respectively); however the incidence of distant recurrence was simi- lar between both arms (4.4% versus 5.5%, respectively).
Authors noted that the extension of treatment with letrozole lead to a statistically significant worsening of bone density. This was in the context of a greater rate of clinical fractures observed in those taking extended letrozole (14% versus 9%; P = .001, respec- tively). Furthermore, although overall quality-of-life assessments were not significantly different between study arms, there were significant in between-group differences over time for bodily pain and the role-emotional subscales (P = .03 and P = .03, respectively). In interpreting these data, it is important to consider that this trial selected a population of patients that were already very familiar with, and likely tolerant of, the side effects of anti-hormone therapy. Additionally, extended courses of anti-hormone therapy are typically associated with suboptimal adherence, indeed MA-17R found adherence rates of 62.5% among those receiving letrozole and 62.3% for placebo.
SABCS 2016: First Results of DATA, IDEAL, and NSABP B-42  More recently at the 2016 SABCS, several studies have reported on extended durations of AI therapy (Table 1). The DATA study randomized 1912  postmenopausal women who had received 2   to 3 years of tamoxifen versus 6 years of anastrozole. The study did not meet its primary endpoint as 5-year DFS was 83.1% in  the 6-year group, and 79.4% in the 3-year group (HR, 0.79; 95% CI, 0.62-1.02, P = 0.07).28 There was some benefit in higher risk groups of patients including those with larger tumors and  those
which were node-positive. Given the biology of ER-positive breast cancer, these are early data and longer follow up is  required. The IDEAL study randomized patients who had completed 5 years of endocrine therapy (either 5 years of tamoxifen or AI,   or tamoxifen followed by AI) to an additional 2.5 versus 5 years of letrozole.29 There was no significant difference in 5-year  DFS (88.4% versus 87.9%; HR, 0.88; 95% CI, 0.64-1.21, P = .43), however, these are relatively early data as well and longer follow up is required. The NSABP B-42 study investigated postmenopausal women who had completed 5 years of endocrine therapy  (either 5 years of AI or tamoxifen followed by AI) to 5 years of letrozole versus placebo.30 Again in this study there was no statistically  sig- nificant difference in DFS (81.3% versus 84.7%; HR, 0.85; 95%  CI, 0.73-0.999; P = .048 where significance level at .0418), again, longer follow up is needed. While these studies did not meet their primary endpoints, these data need to mature, as benefit with extended adjuvant endocrine therapy is typically observed beyond  9 years.25,26

Practical Guidance of Gene Expression Platforms and Future Directions
Studies investigating extended AI therapies are showing modest to no benefit thus far, therefore, decisions to extend AI therapy beyond 5 years should be done on an individual basis, considering patient and tumor characteristics and toxicity. Since the majority of benefit is in chemoprevention, the patient’s desire and eligibility for chemoprevention should be discussed. Patients with bilateral mastectomies for instance, would be less likely to benefit from chemoprevention. In addition, AIs are not benign medications, and these studies have demonstrated the significant effect on bones and certain quality-of-life measures, therefore, considering bone health as well as other side effects patients may be experiencing should weigh in on the decision. Subgroup analysis from the DATA trial suggest that there may be greater benefit in patients who are at high risk as deemed by tumor size of presence of lymph node metastasis, and this may be the group that is most likely to benefit. However, while the concept that higher risk groups may benefit from longer therapy is reasonable, the fact that the benefit may be modest sug- gests there are other mechanisms at play. Indeed, mutations of ESR1 and the PI3K pathway have been implicated in resistance in a subset of hormone receptor-positive breast cancers.31,32 Ultimately targeting resistance mechanisms in defined subsets of hormone receptor-pos- itive breast cancer may be more important than longer duration of endocrine therapies.


A better understanding of disease biology has led to these state of the art approaches to adjuvant therapy. Both the Oncotype Dx and Mammaprint now have prospective data to support their use in clinical practice, albeit with their own set of limitations. They can nevertheless be helpful in patients with hormone receptor-positive and node-negative disease. These tests need to be considered in clin- ical context, and decisions to order and apply them evaluated on an individual basis. Studies such as the OPTIMA trial are comparing Mammaprint, Oncotype DX, PAM50, the IHC4 and various other assays, and will provide information as to how these assays perform against each other.33 In terms of optimizing anti-hormone therapy in postmenopausal women, evidence suggests that extended anti-hor- mone therapies may provide modest protection against breast cancer recurrence; however, this is not necessarily required for all patients, and decisions should be individualized. As we push the boundaries with state of the art molecular biomarkers and treatment strategies, we have continued to make incremental improvements to patients care; however, more research understanding breast cancer biology and molecular mechanisms of resistance are needed to further optimize care.
Author affiliations: Ludimila L. Cavalcante, MD, and Cesar A. Santa-Maria, MD, are with Northwestern University, Robert H. Lurie Comprehensive Cancer Center.
Address correspondence to: Cesar A. Santa-Maria, MD, 676 North St. Clair, Suite 850, Chicago, Illinois 60611; Phone: (312) 695-2379; e-mail: [email protected].
Disclosures: Ludimila L. Cavalcante, MD, and Cesar A. Santa-Ma- ria, MD, report no conflicts of interest.

Adjuvant Chemotherapy in Hormone Receptor-Positive Disease: To Give or not to Give

  1. Bonadonna G, Brusamolino E, Valagussa P, et al, Combination chemotherapy as an adjuvant treatment in operable breast cancer. N Engl J Med. 1976;294(8):405-410.
  2. Sonnenblick, A, M. Piccart, Adjuvant systemic therapy in breast cancer: quo vadis? Ann Oncol. 2015;26(8):1629-1634.
  3. Paik S, Tang G, Shak S, et al. Gene expression and benefit of che- motherapy in women with node-negative, estrogen receptor-positive breast cancer. J Clin Oncol. 2006;10;24(23):3726-3734.
  4. Voduc KD, Cheang MC, Tyldesley S, et al. Breast cancer subtypes and the risk of local and regional relapse. J Clin Oncol. 2010;28(10):1684-1691. doi: 10.1200/JCO.2009.24.9284.
  5. Dalmau E, Armengol-Alonso A, Muñoz M, Seguí-Palmer MÁ. Current status of hormone therapy in patients with hormone recep- tor positive (HR+) advanced breast cancer. Breast. 2014;23(6):710- 720. doi: 10.1016/j.breast.2014.09.006.
  6. Ades F, Zardavas D, Bozovic-Spasojevic I, et al. Luminal B breast cancer: molecular characterization, clinical management, and future perspectives. J Clin Oncol. 2014;32(25):2794-2803. doi: 10.1200/ JCO.2013.54.1870.
  7. Inwald EC1, Klinkhammer-Schalke M, Hofstädter F, et al. Ki-67 is a prognostic parameter in breast cancer patients: results of a large population-based cohort of a cancer registry. Breast Cancer Res Treat. 2013;139(2):539-552. doi: 10.1007/s10549-013-2560-8.
  8. Caan BJ, Sweeney C, Habel LA, et al. Intrinsic subtypes from the PAM50 gene expression assay in a population-based breast cancer survivor cohort: prognostication of short- and long-term outcomes. Cancer Epidemiol Biomarkers Prev. 2014;23(5):725-734. doi: 10.1158/1055-9965.EPI-13-1017.
  9. Paik S, Shak S, Tang G, et al. A multigene assay to predict recur- rence of tamoxifen-treated, node-negative breast cancer. N Engl J Med. 2004;351(27):2817-2826.
  10. Sparano JA, Gray RJ, Makower DF, et al. Prospective valida- tion of a 21-gene expression assay in breast cancer. N Engl J Med. 2015;373(21):2005-2014. doi: 10.1056/NEJMoa1510764.
  11. Ramsey SD, Barlow WE, Gonzalez-Angulo AM, et al. Integrat- ing comparative effectiveness design elements and endpoints into a phase III, randomized clinical trial (SWOG S1007) evaluating Oncotype Dx-guided management for women with breast cancer involving lymph nodes. Contemp Clin Trials. 2013;34(1):1-9. doi: 10.1016/j.cct.2012.09.003.
  12. Albain KS, Barlow WE, Shak S, et al. Prognostic and predictive value of the 21-gene recurrence score assay in postmenopausal wom- en with node-positive, oestrogen-receptor-positive breast cancer on chemotherapy: a retrospective analysis of a randomised trial. Lancet Oncol. 2010;11(1):55-65. doi: 10.1016/S1470-2045(09)70314-6.
  13. Gage MM, Rosman M, Mylander WC, et al. A validated model for identifying patients unlikely to benefit from the 21-gene recurrence score assay. Clin Breast Cancer. 2015;15(6):467-472. doi: 10.1016/j.clbc.2015.04.006.
  14. Dowsett M, Salter J, Zabaglo L, et al. Predictive algorithms for adjuvant therapy: TransATAC. Steroids. 2011;76(8):777-780. doi: 10.1016/j.steroids.2011.02.032.
  15. Tian S, Roepman P, Van’t Veer LJ, Bernards R, de Snoo F, Glas AM. Biological functions of the genes in the mammaprint breast cancer profile reflect the hallmarks of cancer. Biomark Insights. 2010;5:129-138. doi: 10.4137/BMI.S6184.
  16. Buyse M, Loi S, van’t Veer L, Viale G, et al. Validation and clini- cal utility of a 70-gene prognostic signature for women with node-neg- ative breast cancer. J Natl Cancer Inst. 2006;98(17):1183-1192.
  17. Cardoso F, van’t Veer LJ, Bogaerts J, et al. 70-gene signature as an aid to treatment decisions in early-stage breast cancer. N Engl J Med. 2016;375(8):717-729. doi: 10.1056/NEJMoa1602253.
  18. Early Breast Cancer Trialists’ Collaborative Group (EBCTCG), Peto R, Davies C, et al. Comparisons between different polychemo- therapy regimens for early breast cancer: meta-analyses of long-term outcome among 100,000 women in 123 randomised trials. Lancet. 2012;379(9814):432-444.  doi: 10.1016/S0140-6736(11)61625-5.
  19. Jordan VC. Tamoxifen (ICI46,474) as a targeted therapy to treat and prevent breast cancer. Br J Pharmacol. 2006;147 Suppl 1:S269-276.
  20. Burstein HJ, Temin S, Anderson H, et al. Adjuvant endocrine therapy for women with hormone receptor-positive breast cancer: american society of clinical oncology clinical practice guideline focused update. J Clin Oncol. 2014;32(21):2255-2269. doi: 10.1200/ JCO.2013.54.2258.
  21. Dowsett M1, Cuzick J, Ingle J, et al. Meta-analysis of breast cancer outcomes in adjuvant trials of aromatase inhibitors  versus tamoxifen. J Clin Oncol. 2010;28(3):509-518. doi: 10.1200/ JCO.2009.23.1274.
  22. Early Breast Cancer Trialists’ Collaborative Group (EBCTCG), Davies C, Godwin J, et al. Relevance of breast cancer hormone receptors and other factors to the efficacy of adjuvant tamox- ifen: patient-level meta-analysis of randomised trials. Lancet. 2011;378(9793):771-784. doi: 10.1016/S0140-6736(11)60993-8.
  23. Early Breast Cancer Trialists’ Collaborative Group (EBCTCG), Dowsett M, Forbes JF, et al. Aromatase inhibitors versus tamoxifen in early breast cancer: patient-level meta-analysis of the randomised trials. Lancet. 2015;386(10001):1341-1352. doi: 10.1016/S0140- 6736(15)61074-1.
  24. Brewster AM1, Hortobagyi GN, Broglio KR, et al. Residual risk of breast cancer recurrence 5 years after adjuvant therapy. J Natl Cancer Inst. 2008;100(16):1179-1183. doi: 10.1093/jnci/djn233.
  25. Davies C, Pan H, Godwin J, et al. Long-term effects of continu- ing adjuvant tamoxifen to 10 years versus stopping at 5 years after diagnosis of oestrogen receptor-positive breast cancer: ATLAS, a randomised trial. Lancet. 2013;381(9869):805-816.
  26. Gray RG, et al., aTTom: Long-term effects of continuing adju- vant tamoxifen to 10 years versus stopping at 5 years in 6,953 wom- en with early breast cancer. J Clin Oncol 31, 2013 (suppl; abstr 5).
  27. Goss PE, Ingle JN, Pritchard KI, et al. Extending Aro- matase-Inhibitor Adjuvant Therapy to 10 Years. N Engl J Med. 2016;375(3):209-219. doi: 10.1056/NEJMoa1604700.
  28. Tjan-Heijnen VC, Van Hellemond IE, Peer PG, et al. First results from the multicenter phase III DATA study comparing 3 ver- sus 6 years of anastrozole after 2-3 years of tamoxifen in postmeno- pausal women with hormone receptor-positive early breast cancer. S1-03, P2-09-04, 2016 SABCS.
  29. Blok EJ, van de Velde CJH, Meershoek-Klein Kranenbarg EM, et al. Optimal duration of extended letrozole treatment after 5 years of adjuvant endocrine therapy; results of the randomized phase III IDEAL trial (BOOG 2006-05). S1-04, P2-09-01, 2016 SABCS.
  30. Mamounas EP, Bandos H, Lembersky BC, et al. A randomized, double-blinded, placebo-controlled clinical trial to evaluate extend- ed adjuvant endocrine therapy (5 years of letrozole) in postmeno- pausal women with hormone-receptor positive breast cancer who have completed previous adjuvant endocrine therapy: Initial results of NRG oncology/NSABP B-42. S1-05, 2016 SABCS.
  31. Fribbens C1, O’Leary B1, Kilburn L, et al. Plasma ESR1 mu- tations and the treatment of estrogen receptor-positive advanced breast cancer. J Clin Oncol. 2016;34(25):2961-2968. doi: 10.1200/ JCO.2016.67.3061.
  32. Guerrero-Zotano A, Mayer IA, Arteaga CL. PI3K/AKT/mTOR: role in breast cancer progression, drug resistance, and treatment. Cancer Metastasis Rev. 2016 Nov 28.
  33.  Bartlett JM, Bayani J, Marshall A. Comparing breast cancer multiparameter tests in the OPTIMA prelim trial: no test is more equal than the others. J Natl Cancer Inst. 2016;108(9). pii: djw050. doi: 10.1093/jnci/djw050.
  34. Breast International Group (BIG) 1-98 Collaborative Group1, Thürlimann B, Keshaviah A, et al. A comparison of letrozole and tamoxifen in postmenopausal women with early breast cancer. N Engl J Med. 2005;353(26):2747-2757.
  35. Baum M, Budzar AU, Cuzick J, et al. Anastrozole alone or in com- bination with tamoxifen versus tamoxifen alone for adjuvant treatment of postmenopausal women with early breast cancer: first results of the ATAC randomised trial. Lancet. 2002;359(9324):2131-2139.
  36. Coombes RC, Hall E, Gibson LJ, et al. A randomized trial of exemestane after two to three years of tamoxifen therapy in postmenopausal women with pri mary breast cancer. N Engl J Med. 2004;350(11):1081-1092.
  37. Boccardo F, Rubagotti A, Puntoni M, et al. Switching to anas- trozole versus continued tamoxifen treatment of early breast cancer: preliminary results of the Italian Tamoxifen Anastrozole Trial. J Clin Oncol. 2005;23(22):5138-5147.
  38. Goss PE, Ingle JN, Martino S, et al. A randomized trial of letro- zole in postmenopausal women after five years of tamoxifen therapy for early-stage breast cancer. N Engl J Med. 2003;349(19):1793-1802.

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