Gene signature for risk stratification and treatment of breast cancer: Incorporating tumor biology in clinical decision-making Drukker, Caroline

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1 UvA-DARE (Digital Academic Repository) Gene signature for risk stratification and treatment of breast cancer: Incorporating tumor biology in clinical decision-making Drukker, Caroline Link to publication Citation for published version (APA): Drukker, C. A. (2014). Gene signature for risk stratification and treatment of breast cancer: Incorporating tumor biology in clinical decision-making General rights It is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), other than for strictly personal, individual use, unless the work is under an open content license (like Creative Commons). Disclaimer/Complaints regulations If you believe that digital publication of certain material infringes any of your rights or (privacy) interests, please let the Library know, stating your reasons. In case of a legitimate complaint, the Library will make the material inaccessible and/or remove it from the website. Please Ask the Library: or a letter to: Library of the University of Amsterdam, Secretariat, Singel 425, 1012 WP Amsterdam, The Netherlands. You will be contacted as soon as possible. UvA-DARE is a service provided by the library of the University of Amsterdam ( Download date: 01 Feb 2019

2 Chapter 1

3 Introduction and outline

4 8 Chapter 1

5 Breast cancer Breast cancer is the most frequently diagnosed cancer among women worldwide. 1 Over the past two decades, the incidence rate in the Netherlands increased from 56 per women diagnosed with invasive breast cancer in 1991 to 83 per in This increasing incidence may (partly) be explained by the introduction of population-based screening programs in 1990, which resulted in an increase in the detection of early stage breast cancer after full coverage was achieved in Another important observation is a decrease in breast cancer mortality-rates, from 45 per women in 1991 to 38 per women in , which may be explained by early detection due to the implementation of screening programs as well as the improvement and more extensive use of adjuvant systemic treatment. 3,4 1 Adjuvant systemic therapy After primary treatment consisting of surgery with or without radiotherapy to achieve locoregional control most breast cancer patients are nowadays systemically treated in the adjuvant or neoadjuvant setting. Adjuvant systemic therapy (AST), including endocrine therapy, chemotherapy and/or trastuzumab, is used to control micrometastatic disease and improve long-term outcome. 5 Data from the Early Breast Cancer Trialists Collaborative Group (EBCTCG) confirmed the survival benefit of AST by showing a significant better disease-free and overall survival for patients treated with chemotherapy and/or endocrine therapy in different subgroups. 4 Guidelines in breast cancer treatment The selection of those patients at a high risk of recurrence who are most likely to benefit from AST has traditionally been based on clinicopathological factors such as age, tumor size, grade, estrogen-receptor status (ER), progesterone-receptor status (PR), Human Epidermal growth factor Receptor-2 (HER2) and the status of the axillairy lymph nodes. 6 There are multiple breast cancer guidelines and clinical tools that use these clinicopathological factors to estimate the risk of recurrence and provide a related recommendation for AST. 7-9 The components used in these guidelines are all very similar, but show slight differences in their definitions of high and low risk. Most guidelines only identify a small group of patients who are at a low risk of recurrence and for whom AST is of limited value. Consequently, a majority of patients are classified as high risk and therefore become eligible for AST. This will result in a substantial number of patients being treated with AST while they are unlikely to derive significant benefit from it. The differences in the definitions of low risk used by established guidelines create a non-overlapping group of patients at a low or high risk, indicating a suboptimal predictive accuracy for the individual patient. 7,10,11 For example, the online decision-making tool Adjuvant! Online uses age, tumor size, grade, ER and nodal status to estimate the 10-year survival probability of a given patient and the possible survival-benefit that can be derived from adjuvant endocrine therapy and chemotherapy, while the Nottingham Prognostic Index (NPI) only provides a high or low risk estimation based on a Introduction and outline 9

6 score which is calculated using only tumor size, grade and nodal status. Detailed information on prognostic factors used by established clinicopathological guidelines is summarized in Table 1. Even when using extensively validated clinicopathological factors, predicting the risk of recurrence for the individual patient remains challenging. Already for a long time, pathologists, clinicians and researchers are aware that breast cancer is a heterogeneous disease. Morphology, receptor expression and molecular subtypes all contribute to the clinical course of breast cancer in the individual patient. Variations in clinical behaviour and outcome have been described for several decades. 12 Guidelines and clinical tools have improved over the past years and are now including clinicopathological factors such as HER2 status and Ki67. 13,14 Nevertheless, HER2 and Ki67 only account for a small part of this heterogeneity and still most guidelines do not adjust for the heterogeneity entirely. Therefore, clinicopathological guidelines have only limited ability to predict individual patient outcomes. 15 Insight in the biology of breast cancer: introducing gene signatures Over the past decades, researchers identified many single genes involved in the proliferation and metastatic capacity of breast cancer. Breast cancer progression is a result however of multiple genetic aberrations, and thus one gene will never be responsible for the entire cancer process. 16,17 Therefore, researchers were looking for methods to evaluate the relationships among and within different cellular pathways. The introduction of micro-array analyses provided a way to evaluate multiple genes in multiple pathways at once in a more robust manner. Micro-array technology is used to develop gene signatures that are related to the metastatic potential of an individual breast cancer. These signatures can refine risk estimations based on standard clinicopathological guidelines. 18 One of these signatures is the 70-gene signature (MammaPrint ), which was developed by van t Veer and colleagues at the Netherlands Cancer Institute (NKI) in Amsterdam, the Netherlands. The 70-gene signature measures the level of expression of a set of genes by semi-quantitatively determining the level of messenger RNA (mrna) transcripts. 19 The intensity of the nucleic acids that hybridize to the individual gene probes are commonly shown in a two-color array. 19 Green reflects low expression and red reflects high expression of that gene in the tumor (Figure 1). After hybridization the slides are scanned with a dual laser scanner (Agilent Technologies) and the data is processed using a specific algorithm providing an index-score which originally ranges from 0 to The 70-gene signature was developed using frozen tumor samples from 78 patients who were diagnosed at the NKI with lymph node-negative breast cancer and who were up to 55 years of age at the time of diagnosis. 44 of these 78 patients remained free of distant metastases for at least 5 years. These patients were defined as good prognosis or low risk. 10 Chapter 1

7 Table 1. Clinicopathological factors used by breast cancer guidelines to estimate the risk of recurrence Guideline Age Size Grade Hist. type ER/PR HER2 Ki67 Nodal status Other factors Low risk is defined as Not specified. ER - - Yes Co-morbidities, CT regimen AOL Yes Yes Yes Ductal, in case of other hist. type, information is available online Luminal A; ER/PR +, HER2 -, low Ki67 Biological subtype - Yes - ER/PR Yes Yes Yes, more than 3+ nodes is high risk Pre- or post menopausal St. Gallen expert panel 2011 NPI - Yes Yes Yes - [0.2 x Size] + Number of nodes + Grade; low risk = score < 3.4 <35 or 35 Yes Yes - - Yes - Yes - 10-years survival probability 85%. N0, <35, grade I tumor 1 cm OR 35 yrs, grade I tumor 2 cm. NABON 2012 Not specified. Suggested: <3% survival benefit in 10-years no chemotherapy; 3-5% chemotherapy discussed as possible option Yes Yes Yes - ER Yes Yes Yes Method of detection, CT regimen PREDICT plus AOL = Adjuvant! Online; NPI=Nottingham Prognostic Index; NABON=Nationaal Borstkanker Overleg Nederland; ER=estrogen receptor; PR=progesterone receptor; HER2=Human Epidermal Growth factor Receptor 2; CT=chemotherapy. 1 Introduction and outline 11

8 Figure 1. Micro-array technology used for the 70-gene signature The remaining 34 patients developed distant metastases within 5 years after diagnosis and were defined as poor prognosis or high risk. 12 Tumors with an index-score >0.4 are classified as 70- gene signature low risk and tumors with an index-score <0.4 as 70-gene signature high risk. The signature was validated by van de Vijver et al. in a consecutive series of 151 lymph node-negative and 144 lymph node-positive breast cancer patients, diagnosed at the NKI, aged up to 53 years at the time of diagnosis. 21 Buyse et al. performed an independent validation in 302 lymph nodenegative patients from 5 European hospitals, aged up to 60 years at the time of diagnosis. 22 The prognostic value of the 70-gene signature has also been retrospectively confirmed in several patient subgroups, such as postmenopausal patients, patients with positive axillary lymph nodes and in case of HER2-positive disease Aside from the 70-gene signature, a few other gene signatures have found their way to the clinic. The characteristics of these tests, including PAM 50, Oncotype Dx, EndoPredict, Breast Cancer Index and MapQuant Dx, are described in Table 2. The analyses presented in this thesis focus on the 70-gene signature. Using the 70-gene signature in the daily clinical practice To prospectively evaluate the feasibility of implementation of the 70-gene signature in the community-based setting, the MicroarRAy PrognoSTics in Breast CancER (RASTER) study was conducted. 29 Between 2004 and eligible patients were included in 16 hospitals in the Netherlands. Implementation of the 70-gene signature appeared feasible, even though the test could only be performed on fresh frozen tumor samples at the time. Recently, also formalin fixed paraffin embedded (FFPE) tumor samples can be used to perform the 70-gene signature Chapter 1

9 Table 2. Characteristics of gene signatures currently available MammaPrint Pam50 Oncotype Dx EndoPredict Breast Cancer Index MapQuant Dx 97-gene (micro-array) or 8-gene (qrt-pcr) signature 11-gene signature 2-gene ratio HOXB13 and IL17R and molecular grade index (MGI) Assay 70-gene signature 55-gene signature 21-gene recurrence score Technique Micro-array qrt-pcr qrt-pcr qrt-pcr qrt-pcr Micro-array/ qrt-pcr Ipsogen (Marseille, FR) Biotheranostics (San Diego, USA) Sividon Diagnostics (Keulen, DU) Genomic Health (Redwood City, USA) ARUP Laboratories (Salt Lake City, USA) Provided by Agendia (Amsterdam, NL) Tissue sample Frozen or FFPE Frozen or FFPE Frozen or FFPE FFPE FFPE Frozen or FFPE 64 pt, ER+ 964 pt, ER+, HER2-588 pt, ER+, N0, treated with tamoxifen for 2-gene ratio. 410 pt ER+, N0 for MGI 447 pt, ER+ from NSABP B-20 study (tamoxifen-treated arm) 189 pt, ER+/-, HER2 +/-, T1-2N0-1 Training set 78 pt, T1-2N0, <55 yrs ER +/- 597 pt, ER+ 265 pt, ER+, N0, treated with tamoxifen 1702 pt, ER+, HER2-, treated with tamoxifen (2 series) 668 pt, ER+ from NSABP B-14 study (treated with tamoxifen) 761 pt for prognosis 133 pt for prediction ER+/-, HER2 +/-, T1-2N0-1 Validation set 295 pt, T1-2N0-1, <53 yrs, ER +/- Low grade GGI or high grade GGI Continuous variable divided in 3 groups; High, Intermediate, Low risk Continuous variable divided in 2 groups; High and Low risk (EP score) Output High and Low risk Continuous variable Continuous variable divided in 3 groups; High, Intermediate, Low risk Molecular grading of ER+, grade 2 tumors Prognosis prediction of ER+, N0 pt treated with tamoxifen Prognosis prediction of ER+, HER2- pt treated with tamoxifen EP clin score by combining EP score with clinicopathological factors Prognosis prediction of ER+, N0 pt treated with tamoxifen Prognosis prediction of N0 pt, ER+, treated with endocrine therapy Prognosis prediction of T1-2N0 pt, ER+/-,<61 yrs Initially developed for xx xx xx mrna levels ER, PR and HER2 mrna levels ER, PR and HER2 (TargetPrint), intrinsic subtypes (BluePrint) Additional information ER+ pt, treated with aromatase-inhibitors Possibly also prognostic for late recurrences ER+ tumor in postmenopausal women xx ER+ and patients with up to 3 pos. axillary lymph nodes Postmenopausal ER+ pt, treated with aromatase-inhibitors Patients with up to 3 pos. axillary lymph nodes, patients who are yrs, and for HER2+ disease Prognostic value in other subgroups FFPE=formalin fixed parafin embedded; pt=patient; ER=estrogen receptor; HER2=Human Epidermal Growth Factor receptor 2 1 Introduction and outline 13

10 Shortly after confirmation of its feasibility in the RASTER study, the 70-gene signature was subjected to an international, multicenter, randomized-controlled trial called Microarray in Node-negative and 1-3 lymph node positive Disease may Avoid Chemotherapy (MINDACT). Patients enrolled in the MINDACT trial had their risk of recurrence assessed by the known online decision making tool Adjuvant! Online and the 70-gene signature. In case of a concordant low risk estimation patients would only receive endocrine therapy, while in case of a concordant high risk estimation patients would receive adjuvant chemotherapy with or without endocrine therapy. If the clinicopathological risk estimation was discordant with the 70-gene signature risk estimation patients were randomized between treatment according to the risk estimation by the 70-gene signature or treatment according to the clinicopathological risk estimation. On July 1 st 2011, the required 6673 patients were successfully enrolled in the trial. The MINDACT trial will evaluate whether adjuvant chemotherapy can safely be omitted in patients with a tumor that is low risk according to the 70-gene signature, while clinical guidelines (in this case Adjuvant! Online) assessed this tumor as high risk. Meanwhile, better prognostication is desired in routine clinical practice and for this reason the 70-gene signature is increasingly applied when there is uncertainty regarding the indication of AST. Several studies from the Netherlands Cancer Institute have shown the impact of the introduction of the 70-gene signature on the quality of life of patients and the cost-effectiveness of genomic testing was confirmed multiple times On the other hand, the effect on clinical decision-making had not systematically been studied. Rationale and outline of this thesis The aim of this thesis is to evaluate outcome prediction and clinical relevance of the 70-gene signature for locoregional and distant recurrence, its influence on risk assessment and AST recommendations, and its additional value to established clinical guidelines used in breast cancer treatment. In addition, we used the 70-gene signature to gain better insight in the biological background of tumors detected in a population-based screening program. The first part of this thesis focuses on the current applicability of the 70-gene signature in daily clinical practice and the impact of the 70-gene signature on clinical decision-making. Chapter 2 of this thesis provides a current overview of the prognostic value of the 70-gene signature in different subgroups of patients as described in recently published, retrospective studies. Chapter 3 provides the first prospective evidence of the prognostic value of the 70-gene signature. The 5-year follow-up data of the RASTER study shows the outcome of patients for whom the 70- gene signature was used to decide whether or not an individual patient should receive adjuvant systemic treatment. In this chapter the 70-gene signature is compared to Adjuvant! Online. Because Adjuvant! Online is the most commonly used, but not the only guideline in breast cancer, we also compared the additional value of the 70-gene signature to other established guidelines in chapter 4. As described earlier, clinicopathological guidelines vary in their risk estimations. At 14 Chapter 1

11 this point in time, there is no data on the agreement among oncologists using clinicopathological factors for risk estimations and the impact of the 70-gene signature on clinical decision-making. Therefore, agreement among oncologists before and after providing the 70-gene signature result was evaluated in chapter 5. Also, we aimed to evaluate long-term outcome of patients for whom a 70-gene signature result was available. Therefore we updated the original consecutive series as published by van de Vijver et al. in 2002 (chapter 6). 1 The second part of this thesis focuses on new areas where the 70-gene signature may improve the biological understanding of breast cancer. Method of detection has proven to be an independent prognostic factor in breast cancer. Patients with a screen-detected cancer have more favorable outcome, independent of known clinicopathological factors such as age, size and ER-status. To investigate whether this observation is supported by a more favorable tumor biology in screen-detected cancers, we described the proportions of high, low and ultralow risk according to the 70-gene signature among screen-detected and interval cancers in the Dutch MINDACT cohort in chapter 7. Since a transition from film-screen mammography (FSM) to full field digital mammography (FFDM) took place at the same time as the MINDACT trial was conducted in the Netherlands we were also able to evaluate the impact of this transition on the biological background of the tumors detected in the nation-wide screening program. The 70-gene signature was developed to predict the risk of distant recurrence in breast cancer. Because of the correlation between distant and locoregional recurrence, we hypothesized that the 70-gene signature would also be able to predict the risk of locoregional recurrence after both breast conserving surgery and mastectomy. The results of analyzing this hypothesis in a pooled dataset of all patients included in one of the 70-gene signature validation studies, who were diagnosed and treated at the Netherlands Cancer Institute, is described in chapter 8.* This thesis ends with a general discussion and future prospects in chapter 9 and a summary of all results is presented in chapter 10. *All studies described in this thesis are performed in accordance with the FEDERA codes of conduct. 34 Introduction and outline 15

12 References 1 Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008: GLOBOCAN Int J Cancer 2010; 127: Nederlandse Kankerregistratie beheerd door IKNL 3 Esserman LJ, Shieh Y, Rutgers EJ, Knauer M, Retel VP, Mook S et al. Impact of mammographic screening on the detection of good and poor prognosis breast cancers. Breast Cancer Res Treat 2011; 130: Early Breast Cancer Trialists Collaborative Group (EBCTCG). Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet 2005; 365: Sotiriou C, Piccart MJ. Taking gene-expression profiling to the clinic: when will molecular signatures become relevant to patient care? Nat Rev Cancer 2007; 7: Cleator S, Ashworth A. Molecular profiling of breast cancer: clinical implications. Br J Cancer 2004; 90: D Eredita G, Giardina C, Martellotta M, Natale T, Ferrarese F. Prognostic factors in breast cancer: the predictive value of the Nottingham Prognostic Index in patients with a long-term follow-up that were treated in a single institution. Eur J Cancer 2001; 37: Goldhirsch A, Glick JH, Gelber RD, Coates AS, Senn HJ. Meeting highlights: International Consensus Panel on the Treatment of Primary Breast Cancer. Seventh International Conference on Adjuvant Therapy of Primary Breast Cancer. J Clin Oncol 2001; 19: Ravdin PM, Siminoff LA, Davis GJ, Mercer MB, Hewlett J, Gerson N et al. Computer program to assist in making decisions about adjuvant therapy for women with early breast cancer. J Clin Oncol 2001; 19: Goldhirsch A, Wood WC, Gelber RD, Coates AS, Thurlimann B, Senn HJ. Meeting highlights: updated international expert consensus on the primary therapy of early breast cancer. J Clin Oncol 2003; 21: Olivotto IA, Bajdik CD, Ravdin PM, Speers CH, Coldman AJ, Norris BD et al. Population-based validation of the prognostic model ADJUVANT! for early breast cancer. J Clin Oncol 2005; 23: van t Veer LJ, Dai H, van de Vijver MJ, He YD, Hart AA, Mao M et al. Gene expression profiling predicts clinical outcome of breast cancer. Nature 2002; 415: Integraal Kankercentrum Nederland. NABON richtlijn mammacarcinoom Wishart GC, Bajdik CD, Dicks E, Provenzano E, Schmidt MK, Sherman M et al. PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2. Br J Cancer 2012; 107: Cardoso F. Microarray technology and its effect on breast cancer (re)classification and prediction of outcome. Breast Cancer Res 2003; 5: Hanahan D, Weinberg RA. The hallmarks of cancer. Cell 2000; 100: Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell 2011; 144: Ross JS, Hatzis C, Symmans WF, Pusztai L, Hortobagyi GN. Commercialized multigene predictors of clinical outcome for breast cancer. Oncologist 2008; 13: Harris JR, Lippman ME, Osborne CK, Morrow M. Diseases of the Breast. Fourth ed. Lippincott Williams & Wilkins, Glas AM, Floore A, Delahaye LJ, Witteveen AT, Pover RC, Bakx N et al. Converting a breast cancer microarray signature into a high-throughput diagnostic test. BMC Genomics 2006; 7: Chapter 1

13 21 van de Vijver MJ, He YD, van t Veer LJ, Dai H, Hart AA, Voskuil DW et al. A gene-expression signature as a predictor of survival in breast cancer. N Engl J Med 2002; 347: Buyse M, Loi S, van t Veer L, Viale G, Delorenzi M, Glas AM et al. Validation and clinical utility of a 70-gene prognostic signature for women with node-negative breast cancer. J Natl Cancer Inst 2006; 98: Bueno-de-Mesquita JM, Linn SC, Keijzer R, Wesseling J, Nuyten DS, van Krimpen C et al. Validation of 70-gene prognosis signature in node-negative breast cancer. Breast Cancer Res Treat 2009; 117: Knauer M, Cardoso F, Wesseling J, Bedard PL, Linn SC, Rutgers EJ et al. Identification of a low-risk subgroup of HER-2-positive breast cancer by the 70-gene prognosis signature. Br J Cancer 2010; 103: Mook S, Schmidt MK, Viale G, Pruneri G, Eekhout I, Floore A et al. The 70-gene prognosis-signature predicts disease outcome in breast cancer patients with 1-3 positive lymph nodes in an independent validation study. Breast Cancer Res Treat 2009; 116: Mook S, Knauer M, Bueno-de-Mesquita JM, Retel VP, Wesseling J, Linn SC et al. Metastatic potential of T1 breast cancer can be predicted by the 70-gene MammaPrint signature. Ann Surg Oncol 2010; 17: Mook S, Schmidt MK, Weigelt B, Kreike B, Eekhout I, van de Vijver MJ et al. The 70-gene prognosis signature predicts early metastasis in breast cancer patients between 55 and 70 years of age. Ann Oncol 2010; 21: Wittner BS, Sgroi DC, Ryan PD, Bruinsma TJ, Glas AM, Male A et al. Analysis of the MammaPrint breast cancer assay in a predominantly postmenopausal cohort. Clin Cancer Res 2008; 14: Bueno-de-Mesquita JM, van Harten WH, Retel VP, van t Veer LJ, van Dam FS, Karsenberg K et al. Use of 70-gene signature to predict prognosis of patients with node-negative breast cancer: a prospective community-based feasibility study (RASTER). Lancet Oncol 2007; 8: Sapino A, Roepman P, Linn SC, Snel M.H.J., Delahaye LJ, van den Akker J. et al. MammaPrint molecular diagnostics on Formalin Fixed Paraffin Embedded tissue. J Mol Diagn. In press. 31 Retel VP, Joore MA, Knauer M, Linn SC, Hauptmann M, Harten WH. Cost-effectiveness of the 70- gene signature versus St. Gallen guidelines and Adjuvant Online for early breast cancer. Eur J Cancer 2010; 46: Retel VP, Joore MA, Drukker CA, Bueno-de-Mesquita JM, Knauer M, van Tinteren H et al. Prospective cost-effectiveness analysis of genomic profiling in breast cancer. Eur J Cancer Retel VP, Groothuis-Oudshoorn CG, Aaronson NK, Brewer NT, Rutgers EJ, van Harten WH. Association between genomic recurrence risk and well-being among breast cancer patients. BMC Cancer 2013; 13: Dutch federation of Biomedical Scientific Societies. Codes of Conduct. 1 Introduction and outline 17