Breast cancer research and a changing treatment pathway

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Breast cancer research and a changing treatment pathway Stuart McIntosh Clinical Senior Lecturer in Surgical Oncology, QUB Consultant Breast Surgeon, BCH

What is the breast surgeon s role in 2016? Surgery is a medieval treatment in a molecular era Breast cancer outcomes are determined by disease biology, tumour burden and response to therapy, not extent of surgery More is better Radical surgery only treatment one size fits all The surgeon s role is to maximise breast and axillary conservation Minimum required for effective disease control - personalised surgery The breast surgeon underpins much clinical breast cancer research

A changing treatment strategy: From the traditional... Surgery Chemotherapy Radiotherapy Endocrine therapy Targeted therapy Surgery is no longer the de facto primary treatment for breast cancer remains key to successful treatment

to the contemporary Surgery as adjuvant treatment Chemotherapy Endocrine therapy Targeted therapy Surgery Radiotherapy Endocrine therapy Shift driven by clinical, scientific and translational research

Benefits of pre-surgical treatment Patient benefits Downstaging of surgery More breast conserving surgery, less mastectomy response-adapted surgery Treatment modification is it working? If not change it! Research benefits evaluation of new treatments and strategies Easy to monitor response Serial biopsies and blood samples Study disease in situ Monitor effects of treatment

Neoadjuvant and window of opportunity studies in breast cancer Multiple cycles or prolonged course of treatment, 18 24 weeks Diagnosis Chemotherapy Chemotherapy Chemotherapy Chemotherapy Chemotherapy Chemotherapy Surgery Biopsy Biopsy Biopsy Diagnosis Short course of treatment Surgery Biopsy Short duration (2 4 weeks) treatment before surgery Biopsy

Neoadjuvant studies a Belfast example The Neo-DDRD study DDRD assay Developed by Almac Diagnostics Uses tumour tissue Predicts response to certain chemotherapy types Both before and after surgery Neo-DDRD study Feasibility study Assess the possibility of using the assay in routine practice Strong translational science component Sample collection during treatment Research to understand pathways underlying the signature

NeoDDRD study a neoadjuvant feasibility study Integrated into standard neoadjuvant treatment Two additional research breast biopsies at diagnosis Blood samples at diagnosis Standard neoadjuvant treatment Serial tissue and blood samples during treatment and at surgery

Neo-DDRD study Open since May 2014 in BCH Recently opened in UHD 25 patients recruited Excellent rates of sample donation Trial extended to 50 patients Example of successful collaborative working Scientific studies on samples will be used to support phase II studies Neoadjuvant and window studies

CIBRAC Chemoprevention In BRCA Carriers BRCA1 80% lifetime risk of breast cancer Majority of cancers oestrogen receptor negative But oestrogen appears key Tumours in breast and ovary Removal of ovaries reduces breast cancer risk Pregnancy may increase breast cancer risk By-products of oestrogen metabolism in cells may cause DNA damage Role of BRCA1 is to respond to DNA damage

CIBRAC Does reducing circulating oestrogen levels reduce DNA damage in breast tissue? Confirm link between oestrogen exposure and DNA damage Better understand how oestrogen and metabolites initiate tumour development Provide evidence to support a larger clinical study looking at chemoprevention in BRCA1 mutation carriers

Planned pilot clinical window study Group 1 6 premenopausal BRCA1 carriers core biopsy, plasma & urine samples Goserelin + anastrazole 3 months Core biopsy, plasma & urine samples Tamoxifen 3 months Core biopsy, plasma & urine samples Group 2 6 premenopausal BRCA1 carriers core biopsy, plasma & urine samples Tamoxifen 3 months Core biopsy, plasma & urine samples Goserelin + anastrazole 3 months Core biopsy, plasma & urine samples DNA damage (comet assays and Immunofluorescence) Plasma and urine metabolite & DNA adduct levels