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
122P - Practice patterns and treatment outcomes of molecular tumour board (MTB)-based personalized cancer therapies: A single-center experience
Presenter: Florian Moik
Session: Poster session 08
123P - Pan-cancer homologous recombination deficiency (HRD) evaluation in patients enrolled in a routine molecular screening program
Presenter: Paula Romero-Lozano
Session: Poster session 08
124P - Incidence of activating frameshift and nonsense mutations in clinically actionable oncogenes
Presenter: Sjors Kas
Session: Poster session 08
125P - Comparison of microarray and next-generation sequencing-based approaches for detection of homologous recombination deficiency
Presenter: Caleb Kidwell
Session: Poster session 08
126P - Genomic landscape and prognostic impact of HER2 low-expressing tumors
Presenter: Aditya Shreenivas
Session: Poster session 08
127P - Clinical utility of circulating tumor DNA (ctDNA) next generation sequencing (NGS) to inform treatment decisions for patients (pts) with advanced solid tumors
Presenter: Diego Gomez Puerto
Session: Poster session 08
128P - Whole blood transcriptomics identifies transcriptional patterns linked to outcomes in patients receiving immune checkpoint inhibitors
Presenter: Sara Hone Lopez
Session: Poster session 08
129P - Integrating large data to unveil vulnerabilities for patients with hot tumors resistant to checkpoint inhibition
Presenter: Anlin Li
Session: Poster session 08
130P - Ipilimumab plus nivolumab (Ipi+Nivo) in patients with tumors harboring high tumor mutational burden or load (TMB/TML-H): Results from the Drug Rediscovery Protocol (DRUP)
Presenter: Soemeya Haj Mohammad
Session: Poster session 08
131P - Systemic immune-inflammation index and overall survival with checkpoint inhibitors
Presenter: Oliver Kennedy
Session: Poster session 08