Evidence map›Paper›PMID 23236019›Full record

ArticleJournal of nuclear medicine : official publication, Society of Nuclear Medicine2013

Imaging tumor burden in the brain with 89Zr-transferrin.

Michael J Evans, Jason P Holland, Samuel L Rice, Michael G Doran, Sarah M Cheal, Carl Campos, Sean D Carlin, Ingo K Mellinghoff, Charles L Sawyers, Jason S Lewis

Open access · bronzeAbstract read
In one paragraph

Article in Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  3. Evaluation of differentScientific reports · 2022
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  6. A PET Imaging Strategy for Interrogating Target Engagement and Oncogene Status in Pancreatic Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
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  7. Translational molecular imaging in exocrine pancreatic cancer.European journal of nuclear medicine and molecular imaging · 2018
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  9. NoninvasiveJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2018
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  11. Noninvasive Measurement of mTORC1 Signaling withClinical cancer research : an official journal of the American Association for Cancer Research · 2017
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  12. Investigation of the complexation ofDalton transactions (Cambridge, England : 2003) · 2017
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  13. Siderophores for molecular imaging applications.Clinical and translational imaging · 2017
    Review
  14. Article
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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 at 2 institutions in 1 country.

Michael J EvansHuman Oncology and Pathogenesis Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10065, USA.
Jason P Holland
Samuel L Rice
Michael G Doran
Sarah M Cheal
Carl Campos
Sean D Carlin
Ingo K Mellinghoff
Charles L Sawyers
Jason S Lewis
Memorial Sloan Kettering Cancer Center · USHoward Hughes Medical Institute · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
SPORE In Prostate CancerP50CA092629 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Yu Chen, MICHAEL J MORRIS · 2001 to 2026
$63.0M
Molecular Imaging: Training for OncologyR25CA096945 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI HRICAK, HEDVIG · 2002 to 2013
$5.2M
Memorial Sloan Kettering Small Animal Imaging ResearchR24CA083084 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI KOUTCHER, JASON ARTHUR · 1999 to 2006
$4.4M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA008748NCI NIH HHS P30-CA08748NCI NIH HHS P50 CA092629NCI NIH HHS P50-CA92629NCI NIH HHS R24 CA083084NCI NIH HHS R24-CA83084NCI NIH HHS R25 CA096945NCI NIH HHS R25-CA096945
6 · The paper itself

Abstract

unlabelledA noninvasive technology that indiscriminately detects tumor tissue in the brain could substantially enhance the management of primary or metastatic brain tumors. Although the documented molecular heterogeneity of diseases that initiate or eventually deposit in the brain may preclude identifying a single smoking-gun molecular biomarker, many classes of brain tumors are generally avid for transferrin. Therefore, we reasoned that applying a radiolabeled derivative of transferrin ((89)Zr-labeled transferrin) may be an effective strategy to more thoroughly identify tumor tissue in the brain, regardless of the tumor's genetic background.

methodsTransferrin was radiolabeled with (89)Zr, and its properties with respect to human models of glioblastoma multiforme were studied in vivo.

resultsIn this report, we show proof of concept that (89)Zr-labeled transferrin ((89)Zr-transferrin) localizes to genetically diverse models of glioblastoma multiforme in vivo. Moreover, we demonstrate that (89)Zr-transferrin can detect an orthotopic lesion with exceptional contrast. Finally, the tumor-to-brain contrast conferred by (89)Zr-transferrin vastly exceeded that observed with (18)F-FDG, currently the most widely used radiotracer to assess tumor burden in the brain.

conclusionThe results from this study suggest that (89)Zr-transferrin could be a broadly applicable tool for identifying and monitoring tumors in the brain, with realistic potential for near-term clinical translation.

Indexed as

RadioisotopesTransferrinTumor BurdenZirconiumAnimalsBrain NeoplasmsCell Line, TumorDiagnostic ImagingFluorodeoxyglucose F18GlioblastomaHumansMaleMiceMice, Inbred ICRFluorodeoxyglucose F18RadioisotopesTransferrinZirconium

Identifiers

PMID23236019
PMCPMC3747823
OpenAlexW2115587180

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.