Evidence mapPaperPMID 41214336Full record

ReviewNature reviews. Urology2026

20 years of taxane therapy in prostate cancer - the past, present and future.

Marc Carceles-Cordon, Veronica Rodriguez-Bravo, Daniel P Petrylak, Josep Domingo-Domenech

Abstract readReview
In one paragraph

Review in Nature reviews. Urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

4 authors.

Marc Carceles-CordonUrology Department, Mayo Clinic, Rochester, MN, USA.
Veronica Rodriguez-BravoUrology Department, Mayo Clinic, Rochester, MN, USA.
Daniel P PetrylakMedical Oncology Department, Yale School of Medicine, New Haven, CT, USA.
Josep Domingo-DomenechUrology Department, Mayo Clinic, Rochester, MN, USA. domingo-domenech.josep@mayo.edu.

Funding

Transgenic and Knockout Shared ResourceP30CA015083 · MAYO CLINIC ROCHESTER · 1985 to 2025
$27.9M
Role of Nuclear Pore-Regulated Mechanisms in Prostate Cancer AggressivenessR01CA237398 · NCI · THOMAS JEFFERSON UNIVERSITY · PI Veronica Rodriguez-Bravo · 2021 to 2024
$1.2M
Determine the Microphthalmia Transcription Factor (MITF)-regulated cell rewiring mechanisms in lethal prostate cancerR01CA261925 · NCI · MAYO CLINIC ROCHESTER · 2023 to 2025
$907k
Mechanisms and therapeutic targeting of lethal prostate cancer master regulator transcription factorsR01CA280999 · MAYO CLINIC ROCHESTER · 2025 to 2025
$533k
Mechanism and therapeutic targeting of castration resistance in SPOP-mutated prostate cancerR01CA285345 · MAYO CLINIC ROCHESTER · 2025 to 2025
$492k
Investigating the impact of chromosomal instability on prostate cancer aggressivenessR01CA294563 · MAYO CLINIC ROCHESTER · 2025 to 2025
$485k
Mechanism and therapeutic targeting of abnormal androgenesis in CHD1-deficient prostate cancerR01CA286864 · MAYO CLINIC ROCHESTER · 2025 to 2025
$452k
NCI NIH HHS P30 CA015083NCI NIH HHS R01 CA237398NCI NIH HHS R01 CA261925NCI NIH HHS R01 CA280999NCI NIH HHS R01 CA285345NCI NIH HHS R01 CA286864NCI NIH HHS R01 CA294563
6 · The paper itself

Abstract

2024 marked the twentieth anniversary of FDA approval for taxane therapy, namely docetaxel, in the treatment of advanced prostate cancer. Approval of this treatment modality signified a breakthrough in the field, as it demonstrated for the first time that a non-antiandrogen targeting agent could significantly improve survival of patients with prostate cancer. New evidence has further solidified the role of taxanes, demonstrating that it improves survival when used in combination with androgen-targeting therapy in early-stage metastatic hormone-sensitive prostate cancer. Consequently, taxane therapy is currently considered a gold standard and mainstay in the treatment of prostate cancer. In this Review, we present an up-to-date analysis of the pivotal role of taxanes in the treatment of prostate cancer, discuss reasons why taxanes are effective and discuss how the mechanisms that confer resistance to taxanes in prostate cancer might be exploited to develop more effective therapeutic strategies.

Indexed as

Antineoplastic AgentsProstatic NeoplasmsTaxoidsDrug Resistance, NeoplasmHumansMaleAntineoplastic AgentsTaxoids

Identifiers

PMID41214336
PMCPMC12784451

What Socratic holds

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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 Socratic graph.