Does neoadjuvant chemotherapy reduce axillary lymph node dissection in postmenopausal ER+/HER2 <i>−</i> breast cancer?

U Ujjwal Soni (6University of Oklahoma Health Sciences Center, Oklahama, United States) C Cameron Anzel (University of Oklahoma Health Sciences Center, Oklahoma City, OK) J Joseph Spear (The University of Oklahoma College of Medicine, Oklahoma City, OK) B Braden Herman (The University of Oklahoma College of Medicine, Oklahoma City, OK) C Cameron Kirkendoll (Feist-Weiller Cancer Center at LSUHSC-Shreveport, Shreveport, LA) S Shamanth Manjunatha Reddy (University of Oklahoma Medical Center, Oklahoma City, OK) M Maxmillian Tjauw (University of Oklahoma College of Medicine, Oklahoma City, OK) O Olivia Bowles (OU College of Medicine, Oklahoma City, OK) A Alex Kim (The University of Oklahoma Health Sciences Center, Oklahoma City, OK) C Canon Cothran (University of Oklahoma Health Campus, Oklahoma City, OK) S Sreeja Ponnam (University of Missouri-Kansas City School of Medicine, Kansas City, MO) A Alisha Johar (OU College of Medicine, Oklahoma City, OK) M Michael Machiorlatti (2Hudson College of Public Health, Oklahoma City, United States) S Supriya Koya (OU Health Stephenson Cancer Center, Oklahoma City, OK)

Abstract

e12634 Background: The role of neoadjuvant chemotherapy (NAC) in postmenopausal estrogen receptor–positive/human epidermal growth factor receptor 2–negative (ER+/HER2−) breast cancer is debated. These tumors are typically less chemo-sensitive, with low rates of nodal pathologic complete response. Despite this, abnormal imaging findings may prompt escalation to NAC in patients with limited nodal disease. We evaluated whether NAC in this population meaningfully reduces the need for axillary lymph node dissection (ALND). Methods: We performed a retrospective analysis of postmenopausal ER+/HER2− breast cancer patients treated at a single institution between 2023 and 2025. Inclusion criteria included baseline cN1 disease defined by axillary ultrasound. The primary endpoint was the rate of ALND avoidance, defined as successful downstaging to SLNB alone, compared between patients treated with NAC versus upfront surgery. Statistical comparisons were performed using Fisher’s exact tests. All analyses were conducted using R version 4.5.3 (RStudio). Results: Of 292 eligible patients, 55 (19%) presented with ultrasound-defined cN1 disease. Among this cN1 cohort, 36 (65%) proceeded to upfront surgery without receiving NAC while 19 (35%) received NAC. Among patients who did not receive NAC, 25 (69%) underwent SLNB alone while 11 (31%) required ALND. Paradoxically, the NAC cohort had a higher rate of requiring ALND compared to the upfront surgery group (58% [11/19] vs. 31% [11/36]; p=0.08; Table 1). Successful surgical de-escalation (SLNB alone) was achieved in only 42% of the NAC group compared to 69% of the non-NAC group. Conclusions: In postmenopausal ER+/HER2− breast cancer with limited nodal disease, the use of NAC does not reliably translate into avoidance of ALND. These findings raise concern for imaging-driven escalation of neoadjuvant therapy without consistent surgical de-escalation and highlight the need for more selective use of NAC in this population. Surgical management of cN1 disease by NAC exposure. Cohort n SLNB Alone Required ALND P-value No NAC 36 25 (69%) 11 (31%) NAC 19 8 (42%) 11 (58%) 0.08

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (14)

U

Ujjwal Soni

6University of Oklahoma Health Sciences Center, Oklahama, United States

C

Cameron Anzel

University of Oklahoma Health Sciences Center, Oklahoma City, OK

J

Joseph Spear

The University of Oklahoma College of Medicine, Oklahoma City, OK

B

Braden Herman

The University of Oklahoma College of Medicine, Oklahoma City, OK

C

Cameron Kirkendoll

Feist-Weiller Cancer Center at LSUHSC-Shreveport, Shreveport, LA

S

Shamanth Manjunatha Reddy

University of Oklahoma Medical Center, Oklahoma City, OK

M

Maxmillian Tjauw

University of Oklahoma College of Medicine, Oklahoma City, OK

O

Olivia Bowles

OU College of Medicine, Oklahoma City, OK

A

Alex Kim

The University of Oklahoma Health Sciences Center, Oklahoma City, OK

C

Canon Cothran

University of Oklahoma Health Campus, Oklahoma City, OK

S

Sreeja Ponnam

University of Missouri-Kansas City School of Medicine, Kansas City, MO

A

Alisha Johar

OU College of Medicine, Oklahoma City, OK

M

Michael Machiorlatti

2Hudson College of Public Health, Oklahoma City, United States

S

Supriya Koya

OU Health Stephenson Cancer Center, Oklahoma City, OK