Evidence map›Paper›PMID 39165295›Full record

ReviewBJR open2024

Deuterium MR spectroscopy: potential applications in oncology research.

Almir Galvão Vieira Bitencourt, Arka Bhowmik, Eduardo Flavio De Lacerda Marcal Filho, Roberto Lo Gullo, Yousef Mazaheri, Panagiotis Kapetas, Sarah Eskreis-Winkler, Robert Young, Katja Pinker, Sunitha B Thakur

Abstract readReview
In one paragraph

Review in BJR open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Advances inFrontiers in endocrinology · 2025
    Review
  5. 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

10 authors.

Almir Galvão Vieira BitencourtImaging Department, A. C. Camargo Cancer Center, São Paulo, 01525-001, Brazil.ORCID https://orcid.org/0000-0003-0192-9885
Arka BhowmikDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, United States.
Eduardo Flavio De Lacerda Marcal FilhoImaging Department, A. C. Camargo Cancer Center, São Paulo, 01525-001, Brazil.
Roberto Lo GulloDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, United States.
Yousef MazaheriDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, United States.
Panagiotis KapetasDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, United States.
Sarah Eskreis-WinklerDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, United States.
Robert YoungDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, United States.
Katja PinkerDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, United States.ORCID https://orcid.org/0000-0002-2722-7331
Sunitha B ThakurDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, United States.ORCID https://orcid.org/0000-0001-8090-3696

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Metabolic imaging in clinical practice has long relied on PET with fluorodeoxyglucose (FDG), a radioactive tracer. However, this conventional method presents inherent limitations such as exposure to ionizing radiation and potential diagnostic uncertainties, particularly in organs with heightened glucose uptake like the brain. This review underscores the transformative potential of traditional deuterium MR spectroscopy (MRS) when integrated with gradient techniques, culminating in an advanced metabolic imaging modality known as deuterium MRI (DMRI). While recent advancements in hyperpolarized MRS hold promise for metabolic analysis, their widespread clinical usage is hindered by cost constraints and the availability of hyperpolarizer devices or facilities. DMRI, also denoted as deuterium metabolic imaging (DMI), represents a pioneering, single-shot, and noninvasive paradigm that fuses conventional MRS with nonradioactive deuterium-labelled substrates. Extensively tested in animal models and patient cohorts, particularly in cases of brain tumours, DMI's standout feature lies in its seamless integration into standard clinical MRI scanners, necessitating only minor adjustments such as radiofrequency coil tuning to the deuterium frequency. DMRI emerges as a versatile tool for quantifying crucial metabolites in clinical oncology, including glucose, lactate, glutamate, glutamine, and characterizing IDH mutations. Its potential applications in this domain are broad, spanning diagnostic profiling, treatment response monitoring, and the identification of novel therapeutic targets across diverse cancer subtypes.

Indexed as

cancer diagnosiscancer metabolismdeuterium metabolic imagingdeuterium MRIdeuterium MR spectroscopyIDH mutationstreatment response

Identifiers

PMID39165295
PMCPMC11333568

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.