Abstract 110P
Background
The human epidermal growth factor receptor 2 (HER2/neu), a member of epidermal growth factor receptor protein family, play a role as predictive and prognostic biomarkers in various tumor types, particularly biliary tract cancers (BTCs), a heterogeneous group of poor-prognosis solid tumors with limited treatment options. Accurate evaluating of HER2 overexpression is essential for selection and determination of eligible patients for HER2-directed therapy. Herein, we report the results of an immunohistochemistry (IHC) concordance study comparing the AmoyDx® HER-2(29D8) assay and the well-established Ventana PATHWAY anti-HER-2/neu (4B5) assay using a BTC cohort of 432 samples.
Methods
Performance of the AmoyDx® HER-2 (29D8) assay was compared against the Ventana PATHWAY anti-HER-2/neu (4B5) assay using 432 pre-selected BTC samples. Further ISH testing was successfully performed in 134 of the samples to identify HER2-positive and HER2-negative samples according to standard criteria.
Results
There was a high concordance between results from the AmoyDx 29D8 and PATHWAY 4B5 assays for HER2-negative (IHC 0, 1 +) and HER2-positive (IHC 2 + , 3 +) BTCs (98.38%, 425/432). When combined with the ISH results, the aggrement was even increased to 99.29% (422/425) (Table). In addition, the low concordance (34.63%, 9/26) between the two assays for IHC 1+ samples, indicating that the detecton criteria for HER2 IHC 0 and 1+ still need further clarification, which reminds researchers to carefully select appropriate assays if they focus on BTC with HER2-low expression types. Table: 110P
Comparison of HER2 scorings derived from the indicated assays
Ventana PATHWAY anti-HER-2/neu (4B5) | ||||
+ | - | Total | ||
AmoyDx® HER-2 (29D8) | + | 19 | 2 | 21 |
- | 1 | 403 | 404 | |
Total | 20 | 405 | 425 | |
Positive percent agreement | 95.00% (95%CI: 75.13%, 99.87%) | |||
Negative percent agreement | 99.51% (95%CI: 98.23%, 99.94%) | |||
Overall percent agreement | 99.29% (95%CI: 97.95%, 99.85%) |
Conclusions
Our data demonstrate that AmoyDx 29D8 exhibited high concordance with PATHWAY 4B5, and could provide critical information for the selection of HER2-targeted therapy for BTC patients.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
W. Su, H. Lu, Z. Liu, Z. Tang, Z. Huang: Financial Interests, Personal, Full or part-time Employment: Amoy Diagnostics. L. Ruan, C. Zhu: Financial Interests, Personal, Advisory Board: Amoy Diagnostics. All other authors have declared no conflicts of interest.
Resources from the same session
690P - Ifinatamab deruxtecan (I-DXd; DS-7300) in patients with advanced solid tumors: Updated clinical and biomarker results from a phase I/II study
Presenter: Manish R Patel
Session: Poster session 17
691P - Efficacy of ABBV-400 monotherapy in patients with MET gene amplified advanced solid tumors
Presenter: John Strickler
Session: Poster session 17
692P - First-in-human study of ELU001, a targeted nanoparticle drug conjugate, in subjects with folate receptor α (FRα) overexpressing solid tumors
Presenter: Wen wee Ma
Session: Poster session 17
693P - Preclinical activity of HLX43, a PD-L1-targeting ADC, in multiple PD-1/PD-L1 refractory/resistant models
Presenter: Yongqiang Shan
Session: Poster session 17
694P - Full efficacy analysis of phase I/II trial investigating bexmarilimab, a novel macrophage-guided immunotherapy in refractory solid tumors
Presenter: Petri Bono
Session: Poster session 17
695P - A phase I/Ib study evaluating the safety and tolerability of NIZ985 alone and in combination with spartalizumab (anti–PD-1) in patients (pts) with solid tumors or lymphoma
Presenter: Elena Garralda
Session: Poster session 17
696P - SIM1811-03 (SIM0235), an anti-tumor necrosis factor receptor-2 (TNFR2) monoclonal antibody, in patients with advanced solid tumor and/or cutaneous T cell lymphomas (CTCL): Preliminary results from an on-going first-in-human phase I trial in China
Presenter: Furong Liu
Session: Poster session 17
699P - Immunogenicity and reactogenicity of BNT162b2 COVID-19 mRNA vaccine in long-survivor (LS) patients with metastatic lung cancer (mLC) after primary immunization (PV) and booster (BD): COVALENCE study
Presenter: Emanuele Vita
Session: Poster session 17