Abstract 175P
Background
Ki67 is an important BC marker, especially for adjuvant treatment in HR+, HER2- cases. Working groups have provided guidance for Ki67 immunohistochemistry (IHC) BC scoring to limit pathologist’s variability, but no scoring method has been universally accepted. Rapid and reliable image analysis solutions to support scoring have surfaced for the Ki67 assessment. We compared Ki67 scoring with Aiforia® Platform (AI deep learning image analysis), Halo® (image analysis supervised software) and 2 independent pathologists (patho) in a BC population.
Methods
We stained 114 BC tumors for Ki67 on the Dako Omnis. Three methodologies were used to quantify ki67+ tumor cells: 1) A deep learning approach model was trained for BC and the Ki67 clone by Aiforia; 2) Two pathos (Patho A and Patho B) were trained following the International Ki67 Working Group guidelines. Intra-analysis assessment was done for one patho; 3) The random forest classifier from Halo was used to separate the image into tumor, non-tumor and background with patho approval. After cell segmentation, Ki67 positivity was assessed by thresholding. The time needed to complete the analyses was recorded for each method.
Results
Intra-pathologist analysis showed a very high reproducibility (r2=0.95) while matched pair analysis between two patho was lower (r2=0.86) despite following guidelines. Our study shows a high consistency of Ki67 results between AI and the other methods (patho A-AI, r2=0.92; B-AI, r2=0.90; Halo-AI, r2=0.93). The correlation obtained between Halo scoring was not as good, but within an acceptable range (Halo-A, r2=0.79, Halo-B, r2=0.84). The deep learning AI approach was the quickest even including the model training (total time: 2.5 hrs). Pathos time ranged from 22 to 28 hrs without a major gain in analysis time in the second review. Halo took 28 hours including application development, pathologist verification, and analysis.
Conclusions
Overall, the ki67 tumor analysis approaches were quite comparable. AI-based image analysis tools offer valuable assistance in Ki67 scoring and could reduce inter-pathologist variability. These results demonstrate the time benefit of using an AI-driven method for Ki67 analysis in breast cancer.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
133P - Neoadjuvant pembrolizumab plus lenvatinib in resectable stage III melanoma patients (pts) (NeoPele): Analysis of the peripheral immune profile correlated to pathological response
Presenter: Ines Pires da Silva
Session: Poster session 08
134P - Unraveling functionally distinct metabolic programs to predict immunotherapy response in non-small cell lung cancer (NSCLC)
Presenter: Arutha Kulasinghe
Session: Poster session 08
135P - Soluble PD-L1 (sPD-L1) as a predictive biomarker in patients with non-small cell lung cancer (NSCLC) treated with immune checkpoint inhibitors (ICIs) in the first-line setting
Presenter: Adrien Costantini
Session: Poster session 08
136P - Circulating hPG80 (WNT pathway activation) as a potential new prognostic/predictive factor of immunotherapy (ICI) efficacy: ONCOPRO prospective study
Presenter: Benoit You
Session: Poster session 08
137P - Long circulating-free DNA fragments predict early-progression (EP) and progression-free survival (PFS) in advanced carcinoma treated with immune-checkpoint inhibition (ICI): A new biomarker
Presenter: Sebastien Salas
Session: Poster session 08
138P - Toward predicting immune checkpoint blockade response in oesophageal squamous cell carcinoma: Integrating tumour and blood characteristics
Presenter: Amelie Franken
Session: Poster session 08
139P - Multimodal prognosis modeling of advanced NSCLC treated with first-line immunochemotherapy: Integrating genomic and microenvironmental data
Presenter: Yi Hu
Session: Poster session 08
140P - Mining metastatic lymph nodes for response to immune checkpoint therapy in non-small cell lung cancer
Presenter: Elena Donders
Session: Poster session 08
141P - Circulating immune cells predict immunotherapy benefit in patients with triple negative breast cancer: Preliminary results from the IRIS study
Presenter: Benedetta Conte
Session: Poster session 08