Abstract 6852: Measure of three cell population co-localization for spatial protein imaging data analysis.
Abstract Background: Spatial protein imaging technologies enable detailed study of the tumor microenvironment (TME) to characterize cell abundance and spatial architecture. Pairwise colocalization metrics (e.g., Ripley’s K) miss higher-order patterns, while enumerating all triangles for three cell populations is computationally infeasible on whole-slide images. Metrics using a triangle’s longest edge poorly distinguish compact triples from elongated or dispersed arrangements. Thus, we propose a new trivariate colocalization measure using triangle area. Methods: We developed a Horvitz-Thompson Monte Carlo estimator and benchmarked the unweighted and isoperimetrically weighted area variants against a longest-edge analogue on simulated data. These metrics were applied to a study of primary high-grade serous carcinoma (n=101) to quantify colocalization among T cells (CD3+), cytotoxic T cells (CD3+CD8+), B cells (CD19+), and macrophages (CD68+). Cox PH models evaluated associations between normalized clustering metrics and overall survival at radii of 15 and 25 μm - adjusted for diagnosis age, stage, and debulking. Results: Simulations showed unbiased, consistent colocalization estimates with lower small-radius variance for area-based measures. Monte Carlo sampling achieved a >105-fold runtime reduction versus full enumeration. In the ovarian study, lower three-cell colocalization levels of lymphocytes with macrophages corresponded to small improvements in overall survival, though not significant (Table 1). Narrower confidence intervals were also observed for area-based estimators, with weighted and unweighted area variants performing similarly. Discussion: Our framework enables scalable quantification of higher-order spatial organization in the TME. Despite comparable associations across estimators in the ovarian study, the greater stability of area-based measures supports their use as surrogates of complex cellular architecture in future spatial studies. Citation Format: Kirill Sabitov, Alex Soupir, Lauren C. Peres, Brooke L. Fridley. Measure of three cell population co-localization for spatial protein imaging data analysis [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6852.
Authors
- Brooke L. Fridley (ORCID: https://orcid.org/0000-0001-7739-7956)
- Alex C. Soupir (ORCID: https://orcid.org/0000-0003-1251-9179)
- Lauren Cole Peres (ORCID: https://orcid.org/0000-0002-6620-8600)
- Kirill Sabitov (ORCID: https://orcid.org/0009-0004-9457-7587)
Institutions
- Moffitt Cancer Center (US)
- Mercy Research (US)
Publication Details
- Journal
- Cancer Research
- Published
- 2026-04-03
- DOI
- https://doi.org/10.1158/1538-7445.am2026-6852
- Primary Topic
- Single-cell and spatial transcriptomics
- Type
- article
- Field-Weighted Citation Impact
- 0.00