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 session 17

110P - Detection of HER2 overexpression in biliary tract cancers: Comparison of AmoyDx® HER-2 (29D8) assay with ventana PATHWAY anti-HER-2/neu (4B5) assay

Date

21 Oct 2023

Session

Poster session 17

Topics

Pathology/Molecular Biology

Tumour Site

Hepatobiliary Cancers

Presenters

Hui Dong

Citation

Annals of Oncology (2023) 34 (suppl_2): S215-S232. 10.1016/S0923-7534(23)01929-4

Authors

H. Dong1, W. Su2, H. Lu3, Z. Liu3, Z. Tang3, Z. Huang2, L. Ruan3, C. Zhu2

Author affiliations

  • 1 Department Of Pathology, Shanghai Eastern Hepatobiliary Surgery Hospital, 200438 - Shanghai/CN
  • 2 Department Of Translational Medicine, Amoy Diagnostics Co., Ltd., 361027 - Xiamen/CN
  • 3 Department Of Research And Development, Amoy Diagnostics Co., Ltd., 361027 - Xiamen/CN

Resources

Login to get immediate access to this content.

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

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.

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.