Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster Display

50P - A nationwide retrospective cohort study of the response to neoadjuvant chemotherapy between HER-2 low and HER-2 negative non-metastatic breast cancer in Qatar: A real-world analysis

Date

02 Dec 2023

Session

Poster Display

Presenters

Ahmed Kardousha

Citation

Annals of Oncology (2023) 34 (suppl_4): S1480-S1484. 10.1016/annonc/annonc1375

Authors

A. Kardousha1, W. Shehada2, A. Basha1, S. Nasser1, M.M. El Mistiri3, A. Hamad1, S.B. Bujassoum3, S. Elazzazy1

Author affiliations

  • 1 Pharmacy Department, Hamad Medical Corporation (HMC) - National Center for Cancer Care and Research (Al Amal Hospital), 00000 - Doha/QA
  • 2 Nursing And Inpatient Services Department, Hamad Medical Corporation (HMC) - National Center for Cancer Care and Research (Al Amal Hospital), 00000 - Doha/QA
  • 3 Medical Oncology Department, Hamad Medical Corporation (HMC), 00000 - Doha/QA

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 50P

Background

Breast Cancer is the most diagnosed cancer type worldwide and the second leading cause of cancer-related deaths among women. Anti-HER2 treatment has shifted the treatment paradigm of HER2-positive tumors. Historically, only breast cancer patients with HER2 IHC score of 3+ or with HER2 gene (FISH) amplification have benefited from anti-HER2 agents. However, emerging evidence suggests that even a minimal amplification of HER2 may significantly impact response to therapy and prognosis. This led to the introduction of the new concept of HER2-low breast cancers. Our retrospective analysis aims to unveil the impact of HER2 low expression on the response to neoadjuvant chemotherapy (NACT) in non-metastatic HER2-negative breast cancers.

Methods

All patients’ profiles with non-metastatic, HER2-negative breast cancers who received neo-adjuvant chemotherapy and underwent surgery between the 1st of January 2018 and the 30th of August 2022 were retrospectively reviewed. Patients were stratified into HER2-low and HER2-negative groups based on IHC score and FISH amplification. To compare the two study groups, patients’ response was clinically evaluated using surgical pathology reports. The primary endpoint was the response to NACT reported as the objective response rate (ORR) of HER2-low and HER2-negative tumors.

Results

Out of 262 patients, 236 patients had a response. Among the responders, 32 patients (14%) in the HER2-low group had a complete response compared to 4 patients (14%) in the HER2-negative group, OR 0.7 (95% CI:0.2 – 3), p-value= 0.6. While 132 patients (57%) and 17 patients (59%) had a partial response in the HER2-low and HER2-negative groups respectively, OR 0.7 (95% CI:0.2 – 2), p-value= 0.5. Across both groups, more patients with hormone-positive tumors had a response compared to hormone-negative tumors (p-value=0.01).

Conclusions

Preliminary results did not show any statistically significant impact of HER2 low expression on neoadjuvant chemotherapy response. Nonetheless, statistical significance was observed relative to hormone expression, in accordance with the published literature.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Medical Research Center, Hamad Medical Corporation.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.