ArticleCancer medicine2026
An Open Source Automated Tumor Infiltrating Lymphocytes Algorithm for Prognosis in Primary Small Bowel Adenocarcinoma Using Routine Hematoxylin and Eosin Stained Sections.
Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
13 authors.
Funding
Abstract
objectiveWhile tumor-infiltrating lymphocytes (TILs) are prognostic in various cancers, their role in small bowel adenocarcinoma (SBA) is unexplored. This study evaluates the prognostic significance of digitally quantified TILs in SBA.
methodsUsing digital pathology (QuPath) on hematoxylin and eosin (H&E)-stained slides from 62 SBA cases, we quantified tumor cells, TILs (lymphocytes & plasma cells), and stromal components. Derived variables (eTILs, etTILs, esTILs, eaTILs, sTILs, iTILs, easTILs, and tumor-stroma ratio [TSR]) were correlated with clinicopathological features and survival. To account for multiple comparisons across all statistical tests, false discovery rate (FDR) correction was applied.
resultsSeveral TIL-related parameters showed suggestive associations with clinicopathological features (p < 0.05), though none remained significant after FDR correction. In univariate survival analysis, M stage and TNM stage were strongly associated with disease-free survival (DFS) and remained highly significant after FDR correction (both q < 0.001). Regarding TIL-related parameters, higher eTILs (p = 0.028) and iTILs (p = 0.032) showed suggestive associations with prolonged overall survival (OS) in univariate analysis, and higher iTILs also showed a suggestive association with DFS (p = 0.045); however, none of these associations remained significant after FDR correction. In multivariate analysis, M stage and TNM stage were confirmed as independent prognostic factors for DFS, while eTILs (p = 0.099) and tumor deposit (p = 0.055) showed trends toward independent prognostic significance without reaching statistical significance.
conclusionThis study, for the first time, objectively quantifies TILs in SBA, a rare tumor, using digital pathology and explores the potential prognostic significance of TILs in SBA. TIL-related parameters demonstrate suggestive trends that warrant validation in larger, independent cohorts. These findings provide a foundation for future studies to clarify the role of TILs in SBA.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.