Axillary management in T1-3N1M0 breast cancer patients with needle biopsy proven nodal metastases at presentation after neoadjuvant chemotherapy (ATNEC).

Authors

Amit Goyal

Amit Goyal

Royal Derby Hospital, Derby, United Kingdom

Amit Goyal , Sophie Cramp , Duncan Wheatley , Andrea Marshall , Shama Puri , Natalie Hammonds , Tara Homer , Luke Vale , Romaana Mir , Janice Rose , Helen Teresa Edwards , Samreen Ahmed , Abeer Shaaban , Beatrix Elsberger , Julie Bruce , Sophie Gasson , Valerie Speirs , Jacqui Shaw , Helen Higgins , Janet Dunn

Organizations

Royal Derby Hospital, Derby, United Kingdom, University of Warwick, Coventry, United Kingdom, Royal Cornwall Hospitals NHS Trust, Truro, United Kingdom, Newcastle University, Newcastle University, United Kingdom, Newcastle University, Newcastle, United Kingdom, Mount Vernon Cancer Centre, Northwood, United Kingdom, NCRI Breast Clinical Studies Group, London, United Kingdom, Independent Cancer Patients' Voice, London, United Kingdom, University Hospitals Leicester NHS Trust, Leicester, United Kingdom, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom, Aberdeen Royal Infirmary, Aberdeen, United Kingdom, University of Aberdeen, Aberdeen, United Kingdom, University of Leicester, Leicester, United Kingdom

Research Funding

Other
UK National Institute for Health Research - Health Technology Assessment Programme (NIHR128311).

Background: Neoadjuvant chemotherapy (NACT) results in eradication of cancer in the axillary nodes in 40% to 70% of patients. This raises questions about the benefit of further axillary treatment in those patients with no evidence of residual nodal disease (ypN0) after NACT. Methods:Design: ATNEC is a phase 3, randomised (1:1), multi-centre trial, with embedded economic evaluation, comparing standard axillary treatment (axillary lymph node dissection [ALND] or axillary radiotherapy [ART]) with no further axillary treatment in T1-3N1M0 breast cancer patients with needle biopsy proven axillary nodal metastases, who after NACT have no residual nodal disease (ypN0) on dual tracer sentinel node biopsy (SNB) and removal of at least 3 nodes (sentinel nodes and marked involved node). Stratification: Institution, type of surgery (breast conserving surgery vs mastectomy), receptor status (triple negative vs HER2 positive vs ER positive and/or PR positive and HER2 negative). Inclusion criteria are: Age ≥ 18, Male or female, T1-3N1M0 breast cancer at diagnosis (pre-NACT), FNA or core biopsy confirmed axillary nodal metastases at presentation, ER and HER2 status evaluated on primary tumour, received standard NACT as per local guidelines, ultrasound of the axilla at completion of NACT, dual tracer SNB after NACT and at least 3 nodes removed (sentinel nodes and marked node), no evidence of nodal metastases post NACT (ypN0). Exclusion criteria are: bilateral invasive breast cancer, SNB prior to NACT, marked node not removed except where at least one node removed shows evidence of down-staging with complete pathological response e.g. fibrosis/scarring and at least 3 nodes removed, previous ipsilateral axillary surgery, previous cancer within last 5 years or concomitant malignancy except basal or squamous cell carcinoma of the skin, in situ carcinoma of the cervix, in situ or stage 1 melanoma, contra- or ipsilateral in situ breast cancer. Aims: To assess whether, omitting further axillary treatment (ALND and ART) for patients with early stage breast cancer and axillary nodal metastases on needle biopsy - who after NACT have no residual nodal disease on SNB (ypN0) - is non-inferior to axillary treatment in terms of disease free survival, and reduces the risk of lymphoedema at 5 years. Statistical methods: All analyses will be carried out on an intention-to-treat basis to preserve randomisation, avoid bias from exclusions and preserve statistical power. Radiotherapy quality assurance: Study has in-built radiotherapy QA programme that will be co-ordinated by National Radiotherapy Trials QA (RTTQA) group. Target accrual: 1900. Trial status: Recruiting. Number of sites: 100. Clinical trial information: NCT04109079

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Abstract Details

Meeting

2021 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Breast Cancer—Local/Regional/Adjuvant

Track

Breast Cancer

Sub Track

Local-Regional Therapy

Clinical Trial Registration Number

NCT04109079

Citation

J Clin Oncol 39, 2021 (suppl 15; abstr TPS600)

DOI

10.1200/JCO.2021.39.15_suppl.TPS600

Abstract #

TPS600

Poster Bd #

Online Only

Abstract Disclosures