Evidence map›Paper›PMID 38117803›Full record

ArticlePloS one2023

Image-localized biopsy mapping of brain tumor heterogeneity: A single-center study protocol.

Javier C Urcuyo, Lee Curtin, Jazlynn M Langworthy, Gustavo De Leon, Barrett Anderies, Kyle W Singleton, Andrea Hawkins-Daarud, Pamela R Jackson, Kamila M Bond, Sara Ranjbar and 27 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
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

37 authors at 2 institutions in 1 country.

Javier C UrcuyoMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.ORCID 0000-0003-4017-7284
Lee CurtinMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.ORCID 0000-0002-4083-3803
Jazlynn M LangworthyMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.ORCID 0000-0002-6002-662X
Gustavo De LeonMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.
Barrett AnderiesMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.
Kyle W SingletonMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.
Andrea Hawkins-DaarudMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.
Pamela R JacksonMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.
Kamila M BondMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.
Sara RanjbarMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.
Yvette Lassiter-MorrisMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.
Kamala R Clark-SwansonMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.
Lisa E PaulsonMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.
Chris SeredukDepartment of Cancer Biology, Mayo Clinic, Phoenix, Arizona, United States of America.
Maciej M MrugalaDepartment of Neurology, Mayo Clinic, Phoenix, Arizona, United States of America.
Alyx B PorterDepartment of Neurology, Mayo Clinic, Phoenix, Arizona, United States of America.
Leslie BaxterDepartment of Neurophysiology, Mayo Clinic, Phoenix, Arizona, United States of America.
Marcela SalomaoDepartment of Pathology, Mayo Clinic, Phoenix, Arizona, United States of America.
Kliment DonevDepartment of Pathology, Mayo Clinic, Phoenix, Arizona, United States of America.
Miles HudsonDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Jenna MeyerDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Qazi ZeeshanDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Mithun SatturDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Devi P PatraDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Breck A JonesDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Rudy J RahmeDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Matthew T NealDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Naresh PatelDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Pelagia KouloumberisDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Ali H TurkmaniDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Mark LyonsDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Chandan KrishnaDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Richard S ZimmermanDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Bernard R BendokDepartment of Neurosurgery, Mayo Clinic, Phoenix, Arizona, United States of America.
Nhan L TranDepartment of Cancer Biology, Mayo Clinic, Phoenix, Arizona, United States of America.
Leland S HuDepartment of Radiology, Mayo Clinic, Phoenix, Arizona, United States of America.
Kristin R SwansonMathematical NeuroOncology Lab, Mayo Clinic, Phoenix, Arizona, United States of America.ORCID 0000-0002-2464-6119
Mayo Clinic Hospital · USWinnMed · US

Funding

"Research Supplement to Promote Diversity in Health-Related Research", as part of Moffitt PS-OC, "Cancer as a Complex adaptive System"U54CA193489 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI ANDERSON, ALEXANDER ROBERTSON ALLAN, GATENBY, ROBERT A · 2015 to 2020
$12.5M
The Physi(ologi)cal Microenvironment and its Role in Tumor Invasion and MetastaseU54CA143970 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI GATENBY, ROBERT A · 2009 to 2014
$9.3M
Outreach CoreU54CA274504 · NCI · MAYO CLINIC ARIZONA · PI Pamela Rose Jackson · 2023 to 2026
$8.6M
Quantifying Multiscale Competitive Landscapes of Clonal Diversity in GlioblastomaU01CA220378 · NCI · MAYO CLINIC ARIZONA · PI HU, LELAND, SWANSON, KRISTIN R · 2017 to 2021
$4.3M
Langworthy Diversity Supplement: Image-based models of tumor-immune dynamics in glioblastomaU01CA250481 · NCI · MAYO CLINIC ARIZONA · PI CANOLL, PETER, HU, LELAND · 2021 to 2025
$3.8M
NCI NIH HHS U01 CA220378NCI NIH HHS U01 CA250481NCI NIH HHS U54 CA143970NCI NIH HHS U54 CA193489NCI NIH HHS U54 CA274504
6 · The paper itself

Abstract

Brain cancers pose a novel set of difficulties due to the limited accessibility of human brain tumor tissue. For this reason, clinical decision-making relies heavily on MR imaging interpretation, yet the mapping between MRI features and underlying biology remains ambiguous. Standard (clinical) tissue sampling fails to capture the full heterogeneity of the disease. Biopsies are required to obtain a pathological diagnosis and are predominantly taken from the tumor core, which often has different traits to the surrounding invasive tumor that typically leads to recurrent disease. One approach to solving this issue is to characterize the spatial heterogeneity of molecular, genetic, and cellular features of glioma through the intraoperative collection of multiple image-localized biopsy samples paired with multi-parametric MRIs. We have adopted this approach and are currently actively enrolling patients for our 'Image-Based Mapping of Brain Tumors' study. Patients are eligible for this research study (IRB #16-002424) if they are 18 years or older and undergoing surgical intervention for a brain lesion. Once identified, candidate patients receive dynamic susceptibility contrast (DSC) perfusion MRI and diffusion tensor imaging (DTI), in addition to standard sequences (T1, T1Gd, T2, T2-FLAIR) at their presurgical scan. During surgery, sample anatomical locations are tracked using neuronavigation. The collected specimens from this research study are used to capture the intra-tumoral heterogeneity across brain tumors including quantification of genetic aberrations through whole-exome and RNA sequencing as well as other tissue analysis techniques. To date, these data (made available through a public portal) have been used to generate, test, and validate predictive regional maps of the spatial distribution of tumor cell density and/or treatment-related key genetic marker status to identify biopsy and/or treatment targets based on insight from the entire tumor makeup. This type of methodology, when delivered within clinically feasible time frames, has the potential to further inform medical decision-making by improving surgical intervention, radiation, and targeted drug therapy for patients with glioma.

Indexed as

Brain NeoplasmsGliomaBiopsyBrainBrain MappingDiffusion Tensor ImagingHumansMagnetic Resonance Imaging

Identifiers

PMID38117803
PMCPMC10732423
OpenAlexW4390032849

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.