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1091 Decoding clinical and molecular determinants of tertiary lymphoid structure heterogeneity in pancreatic cancer by integrating multimodal spatial transcriptomics, proteomics, and histopathology imaging

2025· article· W4416075644 on OpenAlexaff
Michael J. Geuenich, Yuxi Zhu, Jennifer L. Gorman, Daniele Di Capua, Dorinda Mullen, Erica S. Tsang, Megan Hopkins, Melanie Spears, Steven Gallinger, Hartland W. Jackson, Klaudia Nowak, Kieran R. Campbell

Bibliographic record

VenueRegular and Young Investigator Award Abstracts · 2025
Typearticle
Language
FieldBiochemistry, Genetics and Molecular Biology
TopicSingle-cell and spatial transcriptomics
Canadian institutionsVector InstitutePrincess Margaret Cancer CentreLunenfeld-Tanenbaum Research InstituteOntario Institute for Cancer ResearchUniversity of Toronto
Fundersnot available
KeywordsHistopathologyPancreatic cancerDiseaseCancerPancreasMolecular imaging

Abstract

fetched live from OpenAlex

Background Pancreatic ductal adenocarcinoma (PDAC) is a malignant neoplasm of the pancreas characterized by late-stage detection, with few treatment options and prognostic biomarkers. Tertiary lymphoid structures (TLS) have been found to be predictive of survival in PDAC, however, their phenotypic heterogeneity, functional significance, and relationship to genomic and transcriptomic subtypes remain poorly understood.Methods Using TLS histopathology detection methods we identified TLS across a cohort of over 600 patients and linked their presence to matched genomics and clinical metadata. We generated GeoMx spatial transcriptomics data for 13 PDAC patients with over 200 regions of interest (ROIs) focused on TLS and tumour. We stained and digitized matched whole-slide hematoxylin and eosin (H&E) images and single-cell spatial proteomic data using Imaging Mass Cytometry (IMC) on serial sections of the same ROIs profiled with GeoMx. Using unsupervised clustering and differential expression analyses we characterized TLS into subgroups.Results We show that we can automate TLS detection in H&E from primary tumour resections and liver metastases biopsies. We quantified the percentage of PDAC samples with TLS, the number of TLS per patient and linked their presence to PDAC transcriptomic subtypes, genomic aberrations and patient metadata. We identified three distinct TLS subgroups based on whole-transcriptome TLS expression profiles, and find that TLS subgroup identity is determined by tumour proximity, and specific pathway activation within the adjacent tumour. Finally, we use IMC to deconvolve the single cell content of each subgroup.Conclusions TLS are a known prognostic factor in PDAC, however, they have never been thoroughly characterized or linked to genomic and transcriptomic PDAC subtypes. We find previously unappreciated heterogeneity in TLS phenotypes and link these to tumour phenotypes in what is the most comprehensive characterization of TLS to date.Ethics Approval Samples were taken from previous studies with patient informed consent and approval from Institutional Review or Research Ethics Boards (REB # 20-0170-E, Sinai Health).

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.010

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0020.001
Open science0.0000.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0030.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.009
GPT teacher head0.269
Teacher spread0.260 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2025
Admission routes1
Has abstractno

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