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
193P - Translational, PK, PD, and immunophenotyping analyses of tuvusertib + niraparib in a phase Ib open-label multicenter dose-escalation study in patients with advanced solid tumors (DDRiver Solid Tumors 301)
Presenter: Anthony Tolcher
Session: Poster session 08
194P - CD8-to-CD20 lymphocyte ratio is a predictive biomarker for lenvatinib and pembrolizumab efficacy and progression-free survival in advanced endometrial cancer: Updated data
Presenter: Liubov Tashireva
Session: Poster session 08
195P - Preclinical efficacy of the trastuzumab duocarmazine SYD985 as monotherapy or in combination with the PARP inhibitor niraparib in HER2-expressing endometrial cancer
Presenter: Eva Colas
Session: Poster session 08
196P - Randomized phase II study of trabectedin/olaparib compared to physician’s choice in subjects with previously treated advanced or recurrent solid tumors harboring DNA repair deficiencies
Presenter: Richard Schlenk
Session: Poster session 08
197P - PRIME-ROSE: Merging clinical outcome data from DRUP-like clinical trials
Presenter: Tina Kringelbach
Session: Poster session 08
198P - Inavolisib in cancers with activating PIK3CA mutations: Results from the CRAFT trial
Presenter: Christoph Heilig
Session: Poster session 08
199P - Association of homologous recombination deficiency status with outcomes for ovarian cancer patients treated with olaparib, and exploration of other biomarkers of relapse and survival
Presenter: qingsheng xie
Session: Poster session 08
200P - Outcomes of patients (pts) with unfavourable, non-squamous cancer of unknown primary (CUP) progressing after induction chemotherapy (CTX) in the global, open-label, phase II CUPISCO study
Presenter: Tilmann Bochtler
Session: Poster session 08
201P - Efficacy of antibody drug conjugate (ADC) by mRNA expression of targeted genes in advanced solid tumors: SCRUM-Japan MONSTAR-SCREEN-2
Presenter: Takao Fujisawa
Session: Poster session 08