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Multiple Instance Learning (MIL) approaches can attend to subdomains in tumor regions that harbor features of metastatic cancer progression. However MIL models treat tissue patches as unordered bags, discarding the spatial layout that defines the metastatic potential. We propose that metastatic risk is inherently dictated by the geometric arrangement of the tumor microenvironment at the interface with tumor cells. Our model is designed to explicitly capture the spatial relationships between tumor cells, tumor associated fibroblasts and infiltrating lymphocytes. For this purpose, we propose Distance aware Tissue Modeling for Multiple Instance Learning(DTMf-MIL), a novel method that reinforces visual features with explicit spatial priors. 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Our model is designed to explicitly capture the spatial relationships between tumor cells, tumor associated fibroblasts and infiltrating lymphocytes. For this purpose, we propose Distance aware Tissue Modeling for Multiple Instance Learning(DTMf-MIL), a novel method that reinforces visual features with explicit spatial priors. 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