Evidence map›Paper›PMID 19336015›Full record

ReviewCurrent oncology reports2009

Novel hormonal approaches in prostate cancer.

Terence W Friedlander, Charles J Ryan

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current oncology reports, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

0 citing papers in PubMed, 6 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 1 country.

Terence W FriedlanderHelen Diller Family Comprehensive Cancer Center, University of California-San Francisco, 1600 Divisadero Street, San Francisco, CA 94115, USA.
Charles J Ryan
University of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is well recognized that the vast majority of prostate cancers rely on activation of the androgen receptor (AR) by circulating androgens for growth and survival. Three proven hormonal strategies to impair AR signaling are decreasing gonadal hormone production, inhibiting androgen-AR interaction, and impairing extragonadal androgen synthesis. In this review, we discuss the current strategies to slow initial and castration-resistant tumor growth through the use of hormonal agents such as the gonadotropin-releasing hormone analogues, antiandrogens, and adrenolytic agents, focusing on defining the optimal timing, combinations, and use of these agents, as well as on novel drug development.

Indexed as

Androgen Receptor AntagonistsAndrogen AntagonistsAndrogensGonadotropin-Releasing HormoneHumansMaleOligopeptidesOrchiectomyProstatic NeoplasmsReceptors, AndrogenSignal Transductionacetyl-2-naphthylalanyl-3-chlorophenylalanyl-1-oxohexadecyl-seryl-4-aminophenylalanyl(hydroorotyl)-4-aminophenylalanyl(carbamoyl)-leucyl-ILys-prolyl-alaninamideAndrogen AntagonistsAndrogen Receptor AntagonistsAndrogensGonadotropin-Releasing HormoneOligopeptidesReceptors, Androgen

Identifiers

PMID19336015
OpenAlexW1967667292

What OpenQuestion holds

Textmetadata
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.