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.
Resources from the same session
497P - Sintilimab in combination with anlotinib in advanced NSCLC treated with first-line PD-1 antibodies: An open, single-arm, phase II trial
Presenter: Ying Jin
Session: Poster Display
Resources:
Abstract
498P - Frailty-adjusted life expectancy and survival in older lung cancer patients: A large-scale electronic health-record based study
Presenter: Thao Tu
Session: Poster Display
Resources:
Abstract
499P - Long-term survival and treatment (tx) patterns after first-line (1L) osimertinib in patients (pts) with epidermal growth factor receptor (EGFR) mutation-positive (m) advanced non-small cell lung cancer (NSCLC): Japanese cohort of a global real-world (rw) observational study
Presenter: Daichi Fujimoto
Session: Poster Display
Resources:
Abstract
500P - The effectiveness and safety of durvalumab after chemoradiotherapy for locoregional recurrence of completely resected non-small cell lung cancer: Real-world, multicenter, observational study (NEJ056)
Presenter: Hidehito Horinouchi
Session: Poster Display
Resources:
Abstract
501P - One-year survival outcomes of unresectable stage III non-small cell lung cancer patients who underwent PD-1 inhibitor plus chemo as induction therapy
Presenter: Xin Wang
Session: Poster Display
Resources:
Abstract
502P - Impact of sarcopenia on the outcome of patients with locally advanced non-small cell lung cancer treated with chemoradiotherapy followed by durvalumab
Presenter: Kentaro Tamura
Session: Poster Display
Resources:
Abstract
503P - Clinical outcomes by infusion timing of immune checkpoint inhibitors in patients with locally advanced NSCLC
Presenter: TSUYOSHI HIRATA
Session: Poster Display
Resources:
Abstract
504P - Real-world outcomes with induction systemic therapy for stage III in eligible for upfront local therapy: Pre vs post immunotherapy era in a tertiary referral centre
Presenter: Praveen Kumar Marimuthu
Session: Poster Display
Resources:
Abstract
505P - Neoadjuvant PD-1 inhibitor (tislelizumab) plus platinum–etoposide in patients with limited-stage small cell lung cancer: A phase II trial
Presenter: Junjie Hu
Session: Poster Display
Resources:
Abstract
506P - Intrathoracic progression is still the most dominant failure pattern after first-line chemo-immunotherapy in extensive-stage small-cell lung cancer: Implications for thoracic radiotherapy
Presenter: Byoung Hyuck Kim
Session: Poster Display
Resources:
Abstract