Evidence map›Paper›PMID 19638458›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2009

Starving the addiction: new opportunities for durable suppression of AR signaling in prostate cancer.

Karen E Knudsen, Howard I Scher

2 registry-linked trialsOpen access · bronzeAbstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 193 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
193citing papers in PubMed, 1 pooled it
18.9field-weighted citation impact, top 1% 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.

NCT01848067 phase1 / phase2completednot on this mapstarted 2013, after this paper: background citation

A Phase I/II Study of Alisertib in Combination With Abiraterone and Prednisone for Patients With Castration-Resistant Prostate Cancer After Progression on Abiraterone

TypeinterventionalSponsorSidney Kimmel Comprehensive Cancer Center at Thomas Jefferson UniversityRan2013 to 2016Enrolled9ConditionsAdenocarcinoma of the Prostate, Hormone-resistant Prostate Cancer, Recurrent Prostate Cancer, Stage IV Prostate CancerArmsAlisertib, Abiraterone acetate, Prednisone
NCT03829930 phase1terminatednot on this mapstarted 2019, after this paper: background citation

A Phase I Study of Entinostat in Combination With Enzalutamide for Treatment of Patients With Castration-Resistant Prostate Cancer

TypeinterventionalSponsorGeorge Washington UniversityRan2019 to 2020Enrolled6ConditionsProstate AdenocarcinomaArmsEntinostat, Enzalutamide
3 · Its place in the literature

Who cites it

193 citing papers in PubMed, 1 synthesis or guideline pooled it, 305 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  6. Enzalutamide in metastatic prostate cancer before chemotherapy.The New England journal of medicine · 2014
    Trial
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  8. Review
  9. Review
  10. Article
  11. Review
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  13. Article
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  17. Impact of cell plasticity on prostate tumor heterogeneity and therapeutic response.American journal of clinical and experimental urology · 2024
    Review
  18. Article
  19. Article
  20. [Diagnostics (Basel, Switzerland) · 2023
    Review

133 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 1 country.

Karen E KnudsenDepartments of Cancer Biology, Urology, and Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA. karen.knudsen@kimmelcancercenter.org
Howard I Scher
Memorial Sloan Kettering Cancer Center · USSidney Kimmel Cancer Center · US

Funding

Cyclin D1: repercussions of AR control and alternative splicing in prostate canceR01CA099996 · NCI · UNIVERSITY OF CINCINNATI · PI KNUDSEN, KAREN E · 2003 to 2013
$2.6M
Endocrine disruptors: AR regulation and prostate cancerR01ES016675 · NIEHS · UNIVERSITY OF CINCINNATI · PI KNUDSEN, KAREN E · 2007 to 2011
$1.9M
Role of BAF57 in AR control and prostate cancer growthR01CA116777 · NCI · UNIVERSITY OF CINCINNATI · PI KNUDSEN, KAREN E · 2006 to 2010
$1.3M
NCI NIH HHS R01 CA099996NCI NIH HHS R01 CA116777NIEHS NIH HHS R01 ES016675
6 · The paper itself

Abstract

Clinical data and models of human disease indicate that androgen receptor (AR) activity is essential for prostate cancer development, growth, and progression. The dependence of prostatic adenocarcinoma on AR signaling at all stages of disease has thereby been exploited in the treatment of disseminated tumors, for which ablation of AR function is the goal of first-line therapy. Although these strategies are initially effective, recurrent tumors arise with restored AR activity, and no durable treatment has yet been identified to combat this stage of disease. New insights into AR regulation and the mechanisms underlying resurgent AR activity have provided fertile ground for the development of novel strategies to more effectively inhibit receptor activity and prolong the transition to therapeutic failure.

Indexed as

Androgen AntagonistsAndrogen Receptor AntagonistsAndrogensAnilidesFlutamideHumansMaleNitrilesProstatic NeoplasmsProtein Structure, TertiaryReceptors, AndrogenSignal TransductionTosyl CompoundsAndrogen AntagonistsAndrogen Receptor AntagonistsAndrogensAnilidesAR protein, humanbicalutamideFlutamideNitrilesReceptors, AndrogenTosyl Compounds

Identifiers

PMID19638458
PMCPMC2842118
OpenAlexW2165823301

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.