Evidence map›Paper›PMID 30082477›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2018

A Visually Apparent and Quantifiable CT Imaging Feature Identifies Biophysical Subtypes of Pancreatic Ductal Adenocarcinoma.

Eugene J Koay, Yeonju Lee, Vittorio Cristini, John S Lowengrub, Ya'an Kang, F Anthony San Lucas, Brian P Hobbs, Rong Ye, Dalia Elganainy, Muayad Almahariq and 28 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 4% of its field
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

79 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. Pooled it
  2. Bounding box-based 3D AI model for user-guided volumetric segmentation of pancreatic ductal adenocarcinoma on standard-of-care CTs.Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] · 2023
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19 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

38 authors at 1 institution in 1 country.

Eugene J Koay *Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas. ekoay@mdanderson.org.
Yeonju Lee *Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Vittorio CristiniCenter for Precision Biomedicine, The University of Texas Health Science Center, Houston, Texas.
John S LowengrubDepartment of Mathematics, University of California, Irvine, California.
Ya'an KangDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
F Anthony San LucasSheikh Ahmed Center for Pancreatic Cancer Research, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Brian P HobbsDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Rong YeDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Dalia ElganainyDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Muayad AlmahariqDeparment of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, Texas.
Ahmed M AmerDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Deyali ChatterjeeDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Huaming YanDepartment of Mathematics, University of California, Irvine, California.
Peter C ParkDepartment of Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Mayrim V Rios PerezDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Dali LiSheikh Ahmed Center for Pancreatic Cancer Research, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Naveen GargDepartment of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Kim A ReissDepartment of Medical Oncology, The University of Pennsylvania Abramson Cancer Center, Philadelphia, Pennsylvania.
Shun YuDepartment of Internal Medicine, The University of Pennsylvania, Philadelphia, Pennsylvania.
Anil ChauhanDepartment of Radiology, The University of Pennsylvania, Philadelphia, Pennsylvania.
Mohamed ZaidDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Newsha NikzadDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Robert A WolffDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Milind JavleDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Gauri R VaradhacharyDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Rachna T ShroffDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Prajnan DasDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jeffrey E LeeDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Mauro FerrariDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, Texas.
Anirban MaitraSheikh Ahmed Center for Pancreatic Cancer Research, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cullen M TaniguchiDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Michael P KimDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Christopher H CraneDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
Matthew H KatzDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Huamin WangDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Priya BhosaleDepartment of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Eric P TammDepartment of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jason B FlemingDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
University of California, Irvine · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Christine Hui · 1994 to 2026
$57.9M
Uncover Strategies Used By Biological SystemsP50GM076516 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LANDER, ARTHUR D · 2007 to 2016
$25.1M
TRAINING OF ACADEMIC SURGICAL ONCOLOGISTST32CA009599 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Ashley M Holder, Jennifer A. Wargo · 1988 to 2026
$13.2M
Texas Center for Cancer NanomedicineU54CA151668 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2010 to 2014
$12.4M
Clinical Validation Center for Early Detection of Pancreatic CancerU01CA200468 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ANIRBAN MAITRA · 2016 to 2026
$11.0M
TRANS-NETWORK PROJECTSU54CA143837 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CURLEY, STEVEN ALAN · 2009 to 2014
$10.8M
Shared Resource Core: Single Cell AnalysisU54CA217378 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI VAN ETTEN, RICHARD A. · 2018 to 2022
$9.7M
Transport Oncophysics CoreU54CA210181 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHANG, JENNY C-N · 2016 to 2020
$9.3M
Imaging and Molecular Correlates of Progression in Cystic Neoplasms of the PancreasU01CA196403 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MAITRA, ANIRBAN · 2015 to 2020
$5.8M
A Targeted Nanomedicine Prototype Against Enzalutamide-resistant Prostate CancerR01CA226537 · NCI · RBHS -CANCER INSTITUTE OF NEW JERSEY · PI ARAP, WADIH, BRINKER, C JEFFREY · 2018 to 2022
$3.2M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA062203NCI NIH HHS R01 CA218004NCI NIH HHS R01 CA221971NCI NIH HHS R01 CA222007NCI NIH HHS R01 CA226537NCI NIH HHS T32 CA009599NCI NIH HHS U01 CA196403NCI NIH HHS U01 CA200468NCI NIH HHS U01 CA213759NCI NIH HHS U54 CA143837NCI NIH HHS U54 CA151668NCI NIH HHS U54 CA210181NCI NIH HHS U54 CA217378NIGMS NIH HHS P50 GM076516
6 · The paper itself

Abstract

purposePancreatic ductal adenocarcinoma (PDAC) is a heterogeneous disease with variable presentations and natural histories of disease. We hypothesized that different morphologic characteristics of PDAC tumors on diagnostic computed tomography (CT) scans would reflect their underlying biology. EXPERIMENTAL

designWe developed a quantitative method to categorize the PDAC morphology on pretherapy CT scans from multiple datasets of patients with resectable and metastatic disease and correlated these patterns with clinical/pathologic measurements. We modeled macroscopic lesion growth computationally to test the effects of stroma on morphologic patterns, hypothesizing that the balance of proliferation and local migration rates of the cancer cells would determine tumor morphology.

resultsIn localized and metastatic PDAC, quantifying the change in enhancement on CT scans at the interface between tumor and parenchyma (delta) demonstrated that patients with conspicuous (high-delta) tumors had significantly less stroma, higher likelihood of multiple common pathway mutations, more mesenchymal features, higher likelihood of early distant metastasis, and shorter survival times compared with those with inconspicuous (low-delta) tumors. Pathologic measurements of stromal and mesenchymal features of the tumors supported the mathematical model's underlying theory for PDAC growth.

conclusionsAt baseline diagnosis, a visually striking and quantifiable CT imaging feature reflects the molecular and pathological heterogeneity of PDAC, and may be used to stratify patients into distinct subtypes. Moreover, growth patterns of PDAC may be described using physical principles, enabling new insights into diagnosis and treatment of this deadly disease.

Indexed as

Tomography, X-Ray ComputedAdenocarcinomaAlgorithmsBiopsyCarcinoma, Pancreatic DuctalCell Line, TumorCombined Modality TherapyDNA Mutational AnalysisExome SequencingHumansImage Processing, Computer-AssistedImmunohistochemistryModels, TheoreticalNeoplasm GradingNeoplasm MetastasisNeoplasm Staging

Identifiers

PMID30082477
PMCPMC6279613
OpenAlexW2886778091

What OpenQuestion holds

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Registered trials

None linked

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.