Evidence map›Paper›PMID 32229068›Full record

ReviewNuclear medicine and biology2021

The quest for improving the management of breast cancer by functional imaging: The discovery and development of 16α-[

John A Katzenellenbogen

Open access · greenAbstract readReview
In one paragraph

Review in Nuclear medicine and biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 61 citations in OpenAlex.

  1. [Breast (Edinburgh, Scotland) · 2026
    Trial
  2. Trial
  3. Trial
  4. The Next Frontier in Quantitative Co-Clinical Imaging to Advance Functional Precision Oncology.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Hybrid [AJNR. American journal of neuroradiology · 2025
    Article
  10. Article
  11. The Role of [Cancers · 2025
    Review
  12. Article
  13. Review
  14. Characterization of an Estrogen Receptor α-SelectiveWorld journal of nuclear medicine · 2024
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Invited Commentary: A Recently Approved PET Imaging Agent to Guide Breast Cancer Therapy.Radiographics : a review publication of the Radiological Society of North America, Inc · 2023
    Article
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

1 author at 1 institution in 1 country.

John A KatzenellenbogenDepartment of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States of America. Electronic address: jkatzene@illinois.edu.
University of Illinois Urbana-Champaign · US

Funding

RATIONAL DESIGN OF BREAST TUMOR IMAGING AGENTSR01CA025836 · NCI · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI KATZENELLENBOGEN, JOHN A. · 1985 to 2017
$4.2M
RADIOPHARMACEUTICALS FOR BREAST TUMOR IMAGING &THERAPYR37CA025836 · NCI · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI KATZENELLENBOGEN, JOHN A. · 1999 to 2006
$2.6M
NCI NIH HHS R01 CA025836NCI NIH HHS R37 CA025836
6 · The paper itself

Abstract

introduction16α-[ METHODS AND

resultsThe development of methods for efficient production of fluorine-18, for conversion of [ ADVANCES IN KNOWLEDGE AND IMPLICATIONS FOR PATIENT CARE: Comparisons between ER levels measured by FES-PET imaging of breast tumors with tissue-specimen ER quantification by IHC and other methods show that imaging provided improved prediction of benefit from endocrine therapies. Serial imaging of ER by FES-PET, before and after dosing patients with antiestrogens, is used to determine the efficacious dose for established antiestrogens and to facilitate clinical development of new ER antagonists. Beyond FES imaging, PET-based hormone challenge tests, which evaluate the functional status of ER by monitoring rapid changes in tumor metabolic or transcriptional activity after a brief estrogen challenge, provide highly sensitive and selective predictions of whether or not there will be a favorable response to endocrine therapies. There is sufficient interest in the clinical applications of FES that FDA approval is being sought for its wider use in breast cancer.

conclusionsFES was the first PET probe for a receptor in cancer, and its development and clinical applications in breast cancer parallel the conceptual evolution of the whole field of receptor-binding radiotracers.

Indexed as

Breast NeoplasmsEstradiolPositron-Emission TomographyReceptors, EstrogenAnimalsFemaleHistory, 20th CenturyHistory, 21st CenturyHumansRadioactive Tracers16-fluoroestradiolEstradiolRadioactive TracersReceptors, EstrogenBreast cancerEndocrine therapyHormone-challenge testRadiopharmaceuticalsReceptor-targetingTamoxifen

Identifiers

PMID32229068
PMCPMC7442693
OpenAlexW3008038106

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.