Evidence map›Paper›PMID 35701722›Full record

ArticleMolecular imaging and biology2022

Pilot Study: PARP1 Imaging in Advanced Prostate Cancer.

Farrokh Dehdashti, Melissa A Reimers, Kooresh I Shoghi, Delphine L Chen, Jingqin Luo, Buck Rogers, Russell K Pachynski, Sreeja Sreekumar, Cody Weimholt, Dong Zhou

Open access · hybridAbstract read
In one paragraph

Article in Molecular imaging and biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. [Communications medicine · 2025
    Article
  6. Article
  7. [Journal of clinical medicine · 2024
    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 at 3 institutions in 1 country.

Farrokh DehdashtiEdward Mallinckrodt Institute of Radiology, Washington University School of Medicine, 510 South Kingshighway Blvd, St. Louis, MO, 63110, USA. dehdashtif@wustl.edu.ORCID 0000-0002-6019-3997
Melissa A ReimersDepartment of Internal Medicine, Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Kooresh I ShoghiEdward Mallinckrodt Institute of Radiology, Washington University School of Medicine, 510 South Kingshighway Blvd, St. Louis, MO, 63110, USA.
Delphine L ChenDepartment of Radiology, University of Washington, Seattle, USA.
Jingqin LuoDepartment of Surgery, Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Buck RogersDepartment of Radiation Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Russell K PachynskiDepartment of Internal Medicine, Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Sreeja SreekumarDepartment of Radiation Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Cody WeimholtDepartment of Pathology and Immunology, Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Dong ZhouEdward Mallinckrodt Institute of Radiology, Washington University School of Medicine, 510 South Kingshighway Blvd, St. Louis, MO, 63110, USA.
Washington University in St. Louis · USMallinckrodt (United States) · USSeattle Cancer Care Alliance · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
NCI NIH HHS P30 CA091842
6 · The paper itself

Abstract

purposePARP inhibitor (PARPi) therapy is approved for patients with metastatic castration-resistant prostate cancer (mCRPC) and homologous recombination repair (HRR) genomic aberrations. However, only a fraction of patients with BRCA1/2 mutations respond to PARPi therapy. In this pilot study, we assess PARP-1 expression in prostate cancer patients with and without HRR genomic alternations using a novel PARP-based imaging agent. PROCEDURES: Nine advanced prostate cancer patients were studied with PET/CT and [

resultsWe found great variability in FTT uptake (SUV

conclusionsFTT-PET/CT may serve as an alternate biomarker for PARP1 expression and a potential method for PARPi treatment selection.

Indexed as

Antineoplastic AgentsProstatic NeoplasmsHumansMalePilot ProjectsPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) Polymerase InhibitorsPositron Emission Tomography Computed TomographyAntineoplastic AgentsPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) Polymerase InhibitorsCancerFTTPARPPARP inhibitor (PARPi) therapyPETPositron emission tomography

Identifiers

PMID35701722
PMCPMC9681698
OpenAlexW4282824643

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.