Evidence map›Paper›PMID 33727309›Full record

ArticleCancer discovery2021

Leukocyte Heterogeneity in Pancreatic Ductal Adenocarcinoma: Phenotypic and Spatial Features Associated with Clinical Outcome.

Shannon M Liudahl, Courtney B Betts, Shamilene Sivagnanam, Vicente Morales-Oyarvide, Annacarolina da Silva, Chen Yuan, Samuel Hwang, Alison Grossblatt-Wait, Kenna R Leis, William Larson and 20 more

Abstract read
In one paragraph

Article in Cancer discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

121 citing papers in PubMed.

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  20. Investigation of aBMC cancer · 2026
    Article

61 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors.

Shannon M Liudahl *Department of Cell, Developmental & Cancer Biology, Oregon Health & Science University, Portland, Oregon.ORCID 0000-0002-8587-8204
Courtney B Betts *Department of Cell, Developmental & Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Shamilene Sivagnanam *Department of Cell, Developmental & Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Vicente Morales-OyarvideDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Annacarolina da SilvaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-0067-0288
Chen YuanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-0708-9648
Samuel HwangDepartment of Pathology, Oregon Health & Science University, Portland, Oregon.
Alison Grossblatt-WaitKnight Cancer Institute, Oregon Health & Science University, Portland, OR.
Kenna R LeisDepartment of Cell, Developmental & Cancer Biology, Oregon Health & Science University, Portland, Oregon.
William LarsonDepartment of Cell, Developmental & Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Meghan B LavoieDepartment of Cell, Developmental & Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Padraic RobinsonDepartment of Cell, Developmental & Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Andressa Dias CostaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Sara A VäyrynenDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Thomas E ClancyDepartment of Surgery, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Douglas A RubinsonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-5337-5231
Jason LinkBrenden-Colson Center for Pancreatic Care, Oregon Health & Science University, Portland, Oregon.
Dove KeithBrenden-Colson Center for Pancreatic Care, Oregon Health & Science University, Portland, Oregon.ORCID 0000-0001-6104-3264
Wesley HortonDepartment of Cell, Developmental & Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Margaret A TemperoHelen Diller Family Comprehensive Cancer Center and Department of Medicine, University of California, San Francisco, California.ORCID 0000-0002-2777-9208
Robert H VonderheideAbramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-7252-954X
Elizabeth M JaffeeSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland.ORCID 0000-0003-3841-6549
Brett SheppardBrenden-Colson Center for Pancreatic Care, Oregon Health & Science University, Portland, Oregon.
Jeremy GoecksComputational Biology Program, Oregon Health & Science University, Portland, Oregon.
Rosalie C SearsKnight Cancer Institute, Oregon Health & Science University, Portland, OR.
Byung S ParkKnight Cancer Institute, Oregon Health & Science University, Portland, OR.ORCID 0000-0003-3516-7516
Motomi MoriKnight Cancer Institute, Oregon Health & Science University, Portland, OR.
Jonathan A Nowak *Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Brian M Wolpin *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Lisa M Coussens *Department of Cell, Developmental & Cancer Biology, Oregon Health & Science University, Portland, Oregon. coussenl@ohsu.edu.ORCID 0000-0003-2389-1865

Funding

Oregon Clinical and Translational Research Institute - The National COVID Cohort Collaborative (N3C)UL1TR002369 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Cynthia D Morris, Christopher G. Slatore · 2017 to 2026
$78.4M
Tissue and Pathology ResourcesP50CA127003 · NCI · DANA-FARBER CANCER INST · PI EL-BARDEESY, NABEEL, SELLERS, WILLIAM R · 2007 to 2023
$33.2M
Transforming Human Pancreatic Cancer Into An Immunologic DiseaseP01CA247886 · NCI · JOHNS HOPKINS UNIVERSITY · PI JAFFEE, ELIZABETH M. · 2021 to 2025
$12.7M
Understanding the Impact of Microscale and Nanoscale Heterogeneity and ResistanceU54CA209988 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI GRAY, JOE W. · 2017 to 2021
$10.3M
Omic and Multidimensional Spatial Atlas of Metastatic Breast CancerU2CCA233280 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI DEMIR, EMEK, MILLS, GORDON B. · 2018 to 2023
$9.7M
Circulating Biomarker Consortium for Pancreatic Cancer Early DetectionU01CA210171 · NCI · DANA-FARBER CANCER INST · PI Michael H. Rosenthal, Brian Matthew Wolpin · 2016 to 2026
$8.7M
Targeting the Immunosuppressive Tumor Microenvironment of Pancreatic Cancer with a Neoadjuvant Platform Clinical TrialR01CA197296 · NCI · JOHNS HOPKINS UNIVERSITY · PI William Reece Burns, Eric Christenson · 2015 to 2026
$5.7M
Hydroxylation regulation of c-MycR01CA186241 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Mu-Shui Dai, ROSALIE C SEARS · 2015 to 2026
$4.2M
Therapeutic Targeting of Macrophage PI3Kgamma in HNSCCR01CA226909 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Kathryn Ann Gold, Judith A VARNER · 2018 to 2026
$3.9M
A Federated Galaxy for user-friendly large-scale cancer genomics researchU24CA231877 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI GOECKS, JEREMY · 2018 to 2022
$3.9M
Comparative analysis between patient-derived models of pancreatic ductal adenocarcinomas and matched tumor specimensU01CA224012 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI BRODY, JONATHAN, COUSSENS, LISA M. · 2019 to 2023
$2.9M
The Role of post-translational activation of Myc in pancreatic cancerR01CA196228 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI SEARS, ROSALIE C · 2015 to 2019
$2.0M
NCATS NIH HHS UL1 TR002369NCI NIH HHS P01 CA247886NCI NIH HHS P50 CA127003NCI NIH HHS R01 CA186241NCI NIH HHS R01 CA196228NCI NIH HHS R01 CA197296NCI NIH HHS R01 CA223150NCI NIH HHS R01 CA226909NCI NIH HHS U01 CA210171NCI NIH HHS U01 CA224012NCI NIH HHS U24 CA231877NCI NIH HHS U2C CA233280NCI NIH HHS U54 CA209988NICHD NIH HHS R21 HD099367
6 · The paper itself

Abstract

Immunotherapies targeting aspects of T cell functionality are efficacious in many solid tumors, but pancreatic ductal adenocarcinoma (PDAC) remains refractory to these treatments. Deeper understanding of the PDAC immune ecosystem is needed to identify additional therapeutic targets and predictive biomarkers for therapeutic response and resistance monitoring. To address these needs, we quantitatively evaluated leukocyte contexture in 135 human PDACs at single-cell resolution by profiling density and spatial distribution of myeloid and lymphoid cells within histopathologically defined regions of surgical resections from treatment-naive and presurgically (neoadjuvant)-treated patients and biopsy specimens from metastatic PDAC. Resultant data establish an immune atlas of PDAC heterogeneity, identify leukocyte features correlating with clinical outcomes, and, through an

Indexed as

Tumor MicroenvironmentCarcinoma, Pancreatic DuctalHumansImmunotherapyLeukocytesPancreatic Neoplasms

Identifiers

PMID33727309
PMCPMC8338775

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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.