Evidence map›Paper›PMID 31337429›Full record

ArticleJournal of experimental & clinical cancer research : CR2019

Anti-PSMA

B Frigerio, S Morlino, E Luison, E Seregni, A Lorenzoni, A Satta, R Valdagni, A Bogni, C Chiesa, M Mira and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. QuantitativeBioconjugate chemistry · 2020
    Article
  12. 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

13 authors at 2 institutions in 1 country.

B FrigerioBiomarkers Unit, Department of Applied Research and Technical Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
S MorlinoRadiation Oncology 1, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
E LuisonBiomarkers Unit, Department of Applied Research and Technical Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
E SeregniNuclear Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
A LorenzoniNuclear Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
A SattaBiomarkers Unit, Department of Applied Research and Technical Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
R ValdagniRadiation Oncology 1, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
A BogniNuclear Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
C ChiesaNuclear Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
M MiraNuclear Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
S CanevariFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
A AlessiNuclear Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
M FiginiBiomarkers Unit, Department of Applied Research and Technical Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy. mariangela.figini@istitutotumori.mi.it.ORCID http://orcid.org/0000-0001-9001-8754
Fondazione IRCCS Istituto Nazionale dei Tumori · ITOspedale Papa Giovanni XXIII · IT

Funding

Fondazione Antonio Carlo Monzino N/AH2020 European Research Council 678109Ministero della Salute RF-2016-02363661
6 · The paper itself

Abstract

backgroundProstate cancer (PCa) is the second leading cause of cancer-related death in the Western population. The use in oncology of positron emission tomography/computed tomography (PET/CT) with emerging radiopharmaceuticals promises accurate staging of primary disease, restaging of recurrent disease and detection of metastatic lesions. Prostate-specific membrane antigen (PSMA) expression, directly related to androgen-independence, metastasis and progression, renders this tumour associate antigen a good target for the development of new radiopharmaceuticals for PET. Aim of this study was to demonstrate in a preclinical in vivo model (PSMA-positive versus PSMA-negative tumours) the targeting specificity and sensitivity of the anti-PSMA single-chain variable fragment (scFv) labelled with

methodsThe

resultsThe uptake fraction of

conclusionsPreclinical in vivo results of our immuno-PET reagent are highly promising. The target to background ratio is improved notably using PET compared to SPECT previously performed. These data suggest that, upon clinical confirmation of sensitivity and specificity, our anti-PSMA

Indexed as

AnimalsAntigens, SurfaceCell Line, TumorGlutamate Carboxypeptidase IIHumansImmunoconjugatesIodine RadioisotopesMaleMiceNeoplasm MetastasisPositron Emission Tomography Computed TomographyProstatic NeoplasmsRadiopharmaceuticalsSingle-Chain AntibodiesTissue DistributionAntigens, SurfaceFOLH1 protein, humanGlutamate Carboxypeptidase IIImmunoconjugatesIodine-124Iodine RadioisotopesRadiopharmaceuticalsSingle-Chain Antibodies124IAntibody fragmentPCaPETscFv

Identifiers

PMID31337429
PMCPMC6651934
OpenAlexW2963310108

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.