Abstract 294P
Background
With the development of anti-HER2 targeted antibody-drug conjugates, HER2 low has attracted a lot of attention in breast cancer (BC). It's significant to study the pathological response of HER2 zero, HER2 low and HER2 positive BC after neoadjuvant treatment and the HER2 status evolution.
Methods
A retrospective study was conducted at National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College. Data from patients who were diagnosed with BC between 2015 and 2021 at our center and who had received neoadjuvant treatment were collected. The pathological complete response (pCR) rate of HER2 zero, HER2 low, and HER2 positive was analyzed. And the analysis of HER2 status evolution were carried out.
Results
1173 patients with BC who had received neoadjuvant treatment were collected. 11.85% of the patients (n=193) achieved pCR, and 88.15% of the patients (n=1034) were non-pCR. Among 526 patients with available baseline biopsy reports and matched pathological reports after neoadjuvant treatment, HER2 low BC was related to the lowest rate of pCR, followed by HER2 zero and HER2 positive BC (13.79% vs. 20.00% vs. 40.20%, respectively, p=0.000). Of the 526 patients, 381 were hormone-receptor-positive BC, and 145 were triple-negative breast cancer (TNBC) on baseline biopsy. In 381 patients with hormone-receptor-positive BC, HER2 low BC was also related to the lowest rate of pCR, followed by HER2 zero and HER2 positive BC as well (9.14% vs. 12.28% vs. 36.22%, respectively, p=0.000). A similar trend was also observed in TNBC without a statistically significant difference. On the converting of HER2 zero, HER2 low and HER2 positive before and after neoadjuvant treatment, HER2 zero has the highest discordance rate and 58.21% of HER2 zero on baseline biopsy converted into the other two types after neoadjuvant treatment. The conversion rates of HER2 low and HER2 positive on baseline biopsy were 28.10% and 14.43%, respectively.
Conclusions
Compared with HER2 zero and HER2 positive, HER2 low has the lowest pCR rate after neoadjuvant treatment. Besides, HER2 zero had the highest incidence of conversion to other HER2 statuses after neoadjuvant treatment.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
292P - Unlocking the potential of circulating miRNAs in predicting response to neoadjuvant chemotherapy in breast cancer: A systematic review and meta-analysis
Presenter: Paola Tiberio
Session: Poster session 02
295P - ESR1, PGR, ERBB2, MKI67 single gene analysis in neoadjuvant-treated early breast cancer patients
Presenter: Rebekks Spiller
Session: Poster session 02
296P - Identification of metabolism-related therapeutic targets to improve response to neoadjuvant chemotherapy in early breast cancers
Presenter: Françoise Derouane
Session: Poster session 02
297P - Prognostic and predictive impact of NOTCH1 in early breast cancer
Presenter: Julia Engel
Session: Poster session 02
298P - Association of luminal-androgen receptor (LAR) subtype with low HER2 in triple-negative breast cancer
Presenter: Lee Min Ji
Session: Poster session 02
299P - Single-cell transcriptomic analysis reveals specific luminal and T cell subpopulations associated with response to neoadjuvant therapy in early-stage breast cancer
Presenter: Xiaoxiao Wang
Session: Poster session 02
300P - Correlation of PD-L1 protein and mRNA expression and their prognostic impact in triple-negative breast cancer
Presenter: Kathleen Schüler
Session: Poster session 02
301P - Epigenetic modifications of IL-17 gene in patients with early breast cancer and healthy controls
Presenter: Ljubica Radmilovic Varga
Session: Poster session 02
302P - Clinicopathological features and outcomes of pregnancy associated breast cancer: Case control study -single institution experience
Presenter: Nashwa Kordy
Session: Poster session 02
303P - Differential prognostic role of PDGFRA alterations in breast cancer subtypes
Presenter: Panagiotis Vlachostergios
Session: Poster session 02