Evidence map›Paper›PMID 30906574›Full record

ArticleJournal of translational science2019

First-in-human phase 0 study of

K A Kurdziel, E Mena, Y McKinney, K Wong, S Adler, T Sissung, J Lee, S Lipkowitz, L Lindenberg, B Turkbey and 8 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of translational science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  8. PET and SPECT Imaging of the EGFR Family (RTK Class I) in Oncology.International journal of molecular sciences · 2021
    Review
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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

18 authors at 4 institutions in 1 country.

K A KurdzielMolecular Imaging Program (MIP), Center for Cancer Research (CCR)/National Cancer Institute (NCI), National Institutes of Health (NIH), USA.
E MenaMolecular Imaging Program (MIP), Center for Cancer Research (CCR)/National Cancer Institute (NCI), National Institutes of Health (NIH), USA.
Y McKinneyMolecular Imaging Program (MIP), Center for Cancer Research (CCR)/National Cancer Institute (NCI), National Institutes of Health (NIH), USA.
K WongMolecular Imaging Program (MIP), Center for Cancer Research (CCR)/National Cancer Institute (NCI), National Institutes of Health (NIH), USA.
S AdlerClinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, USA.
T SissungGenitourinary Malignancies Branch, CCR/NCI, NIH, USA.
J LeeDivision of Nuclear Medicine, Radiology and Imaging Sciences, Clinical Center(CC), NIH, USA.
S LipkowitzWomen's Malignancies Branch, CCR/NCI, NIH, USA.
L LindenbergMolecular Imaging Program (MIP), Center for Cancer Research (CCR)/National Cancer Institute (NCI), National Institutes of Health (NIH), USA.
B TurkbeyMolecular Imaging Program (MIP), Center for Cancer Research (CCR)/National Cancer Institute (NCI), National Institutes of Health (NIH), USA.
S KummarWomen's Malignancies Branch, CCR/NCI, NIH, USA.
D E MilenicRadiation Oncology Branch, CCR/NCI, NIH, USA.
J H DoroshowDivision of Cancer Treatment and Diagnosis and CCR/NCI, NIH, USA.
W D FiggGenitourinary Malignancies Branch, CCR/NCI, NIH, USA.
M J MerinoLaboratory of Pathology, CCR/NCI, NIH, USA.
C H PaikDivision of Nuclear Medicine, Radiology and Imaging Sciences, Clinical Center(CC), NIH, USA.
M W BrechbielRadiation Oncology Branch, CCR/NCI, NIH, USA.
P L ChoykeMolecular Imaging Program (MIP), Center for Cancer Research (CCR)/National Cancer Institute (NCI), National Institutes of Health (NIH), USA.
National Institutes of Health · USCenter for Cancer Research · USNational Institutes of Health Clinical Center · USLeidos (United States) · US

Funding

Instrumentation for microSPECT and microPET imagingZIABC010668 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CHOYKE, PETER L · 2009 to 2025
$11.0M
Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

introductionTumors over-expressing the human epithelial receptor 2 (HER2) or exhibiting amplification or mutation of its proto-oncogene have a poorer prognosis. Using trastuzumab and/or other HER2 targeted therapies can increase overall survival in patients with HER2(+) tumors making it critical to accurately identify patients who may benefit. We report on a Phase 0 study of the imaging agent,

methods

resultsNo safety issues were identified. Visual and semi-quantitative imaging data were concordant with tissue HER2 expression profiling in all but 1 patient. The biodistribution showed intense peak liver activity at the initial imaging timepoint (3.3h) and a single-phase clearance fit of the average time-activity curve (TAC) estimated t

conclusion

Indexed as

CHX-A”-DTPAHER2herceptimolecular imagingoncologytrastuzumab

Identifiers

PMID30906574
PMCPMC6425962
OpenAlexW2898768999

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.