Omitting Sentinel Lymph Node Biopsy after Neoadjuvant Systemic Therapy for Clinically Node Negative HER2 Positive and Triple Negative Breast Cancer: A Pooled Analysis

Author:

Alamoodi Munaser12,Wazir Umar23ORCID,Mokbel Kinan24,Patani Neill25,Varghese Jajini26ORCID,Mokbel Kefah2

Affiliation:

1. Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia

2. The London Breast Institute, Princess Grace Hospital, London W1U 5NY, UK

3. Department of Surgery, Khyber Teaching Hospital, Peshawar 25120, Pakistan

4. College of Medicine and Health, University of Exeter Medical School, Exeter EX1 2LU, UK

5. Department of General Surgery, University College London Hospital, Euston Road, London NW1 2BU, UK

6. Department of General Surgery, Royal Free Hospital, London NW3 2QG, UK

Abstract

Recent advances in systemic treatment for breast cancer have been underpinned by recognising and exploiting subtype-specific vulnerabilities to achieve higher rates of pathologic complete response (pCR) after neo-adjuvant systemic therapy (NAST). This down-staging of disease has permitted safe surgical de-escalation in patients who respond well. Triple-negative (TNBC) or HER2-positive breast cancer is most likely to achieve complete radiological response (rCR) and pCR after NAST. Hence, for selected patients, particularly those who are clinically node-negative (cN0) at diagnosis, the probability of disease in the sentinel node after NAST could be low enough to justify omitting axillary surgery. The aim of this pooled analysis was to determine the rate of sentinel node positivity (ypN+) in patients with TNBC or HER2-positive breast cancer who were initially cN0, achieving rCR and/or pCR in the breast after NAST. MedLine was searched using appropriate search terms. Five studies (N = 3834) were included in the pooled analysis, yielding a pooled ypN+ rate of 2.16% (95% CI: 1.70–2.63). This is significantly lower than the acceptable false negative rate of sentinel lymph node biopsy (SLNB) and supports consideration of omission of SLNB in this subset of patients.

Funder

Breast Cancer Hope Foundation

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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