Evidence map›Paper›PMID 37318243›Full record

ArticleJournal of visualized experiments : JoVE2023

Measurement of Tumor T2* Relaxation Times after Iron Oxide Nanoparticle Administration.

Shakthi Kumaran Ramasamy, Raheleh Roudi, Wipawee Morakote, Lisa C Adams, Laura J Pisani, Michael Moseley, Heike E Daldrup-Link

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Color Maps: Facilitating the Clinical Impact of Quantitative MRI.Journal of magnetic resonance imaging : JMRI · 2025
    Review
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

7 authors at 1 institution in 1 country.

Shakthi Kumaran RamasamyDepartment of Radiology, Molecular Imaging Program at Stanford, Stanford University, School of Medicine.
Raheleh RoudiDepartment of Radiology, Molecular Imaging Program at Stanford, Stanford University, School of Medicine.
Wipawee MorakoteDepartment of Radiology, Molecular Imaging Program at Stanford, Stanford University, School of Medicine.
Lisa C AdamsDepartment of Radiology, Molecular Imaging Program at Stanford, Stanford University, School of Medicine.
Laura J PisaniDepartment of Radiology, Molecular Imaging Program at Stanford, Stanford University, School of Medicine.
Michael MoseleyDepartment of Radiology, Radiological Sciences Laboratory (RSL) at Stanford, Stanford University, School of Medicine.
Heike E Daldrup-LinkDepartment of Radiology, Molecular Imaging Program at Stanford, Stanford University, School of Medicine; Department of Pediatrics, Division of Hematology/Oncology, Stanford University, School of Medicine; heiked@stanford.edu.
Stanford University · US

Funding

Co-Clinical Research Resource for Imaging Tumor Associated MacrophagesU24CA264298 · NCI · STANFORD UNIVERSITY · PI DALDRUP-LINK, HEIKE ELIZABETH, GATIDIS, SERGIOS · 2021 to 2025
$3.2M
NCI NIH HHS U24 CA264298
6 · The paper itself

Abstract

T2* relaxometry is one of the established methods to measure the effect of superparamagnetic iron oxide nanoparticles on tumor tissues with magnetic resonance imaging (MRI). Iron oxide nanoparticles shorten the T1, T2, and T2* relaxation times of tumors. While the T1 effect is variable based on the size and composition of the nanoparticles, the T2 and T2* effects are usually predominant, and T2* measurements are the most time-efficient in a clinical context. Here, we present our approach to measuring tumor T2* relaxation times, using multi-echo gradient echo sequences, external software, and a standardized protocol for creating a T2* map with scanner-independent software. This facilitates the comparison of imaging data from different clinical scanners, different vendors, and co-clinical research work (i.e., tumor T2* data obtained in mouse models and patients). Once the software is installed, the T2 Fit Map plugin needs to be installed from the plugin manager. This protocol provides step-by-step procedural details, from importing the multi-echo gradient echo sequences into the software, to creating color-coded T2* maps and measuring tumor T2* relaxation times. The protocol can be applied to solid tumors in any body part and has been validated based on preclinical imaging data and clinical data in patients. This could facilitate tumor T2* measurements for multi-center clinical trials and improve the standardization and reproducibility of tumor T2* measurements in co-clinical and multi-center data analyses.

Indexed as

Magnetic Resonance ImagingNeoplasmsAnimalsMagnetic Iron Oxide NanoparticlesMiceReproducibility of ResultsSoftware

Identifiers

PMID37318243
PMCPMC10619562
OpenAlexW4377087140

What OpenQuestion holds

Textmetadata
LicenceTDM
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.