A reference-calibrated spatial-statistical framework for quantifying stroma-tumor cell spatial associations from histology and its geometric limits
- 1H. Lee Moffitt Cancer Center
Abstract
Quantifying interactions in biological tissues requires determining whether an interaction exists, the distance over which it operates, and its strength. Existing spatial-statistical approaches can characterize spatial organization but often require interaction range or interaction models to be specified a priori, making them less suited to settings where these quantities are themselves unknown. Here, we present a practical framework that recovers the presence, range, and association strength of spatial bias toward a tissue structure directly from segmented histology. The framework combines four complementary statistics, the resource selection function, nearest-structure distance distributions, the cross J-function, and the radial distribution function, with specimen-specific reference states that preserve tissue stromal architecture while spanning a continuum of known spatial biases. Across controlled in silico tissues, we show that tissue stromal architecture imposes geometric limits on the range of recoverable interactions and that event fraction independently constrains statistical sensitivity. These spatial associations establish fundamental bounds on inference and demonstrate that spatial statistics must be interpreted relative to tissue-specific reference states rather than absolute scales. We apply the framework to proliferating tumor cells relative to CAF-rich stroma during tyrosine kinase inhibitor therapy in an ALK+ NSCLC model and identify a strong stroma-associated proliferation bias extending approximately 30-60 micrometers. The framework broadly applies to any histological setting where events and reference structures can be defined, providing a practical approach to quantify localized interactions directly from tissue stromal architecture.
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BibTeX
@misc{miti2026referencecalibrated,
title = {{A reference-calibrated spatial-statistical framework for quantifying stroma-tumor cell spatial associations from histology and its geometric limits}},
author = {T. Miti and D. Miroshnychenko and B. Desai and A. Marusyk and D. Basanta},
howpublished = {bioRxiv},
year = {2026},
month = oct,
doi = {10.64898/2026.10.09.758046},
url = {https://www.biorxiv.org/content/10.64898/2026.10.09.758046v1},
note = {CC BY-NC-ND},
}
RIS
TY - UNPB
TI - A reference-calibrated spatial-statistical framework for quantifying stroma-tumor cell spatial associations from histology and its geometric limits
AU - T. Miti
AU - D. Miroshnychenko
AU - B. Desai
AU - A. Marusyk
AU - D. Basanta
PY - 2026
DA - 2026/10/09
PB - bioRxiv
DO - 10.64898/2026.10.09.758046
UR - https://www.biorxiv.org/content/10.64898/2026.10.09.758046v1
AB - Quantifying interactions in biological tissues requires determining whether an interaction exists, the distance over which it operates, and its strength. Existing spatial-statistical approaches can characterize spatial organization but often require interaction range or interaction models to be specified a priori, making them less suited to settings where these quantities are themselves unknown. Here, we present a practical framework that recovers the presence, range, and association strength of spatial bias toward a tissue structure directly from segmented histology. The framework combines four complementary statistics, the resource selection function, nearest-structure distance distributions, the cross J-function, and the radial distribution function, with specimen-specific reference states that preserve tissue stromal architecture while spanning a continuum of known spatial biases. Across controlled in silico tissues, we show that tissue stromal architecture imposes geometric limits on the range of recoverable interactions and that event fraction independently constrains statistical sensitivity. These spatial associations establish fundamental bounds on inference and demonstrate that spatial statistics must be interpreted relative to tissue-specific reference states rather than absolute scales. We apply the framework to proliferating tumor cells relative to CAF-rich stroma during tyrosine kinase inhibitor therapy in an ALK+ NSCLC model and identify a strong stroma-associated proliferation bias extending approximately 30-60 micrometers. The framework broadly applies to any histological setting where events and reference structures can be defined, providing a practical approach to quantify localized interactions directly from tissue stromal architecture.
ER -