Evidence map›Paper›PMID 39191549›Full record

ArticleUrologic oncology2024

Treatment Intensification in Metastatic Hormone-Sensitive Prostate Cancer: An Analysis of Real-World Practice Patterns from the CancerLinQ Database.

Corbin J Eule, Elizabeth Molina Kuna, Tyler P Robin, Boris Gershman, Thomas W Flaig, Simon P Kim

Abstract read
In one paragraph

Article in Urologic oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Patient selection for triplet therapy with darolutamide in metastatic castration-sensitive prostate cancer and patterns of administration: a Spanish multicenter study.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

6 authors.

Corbin J EuleUniversity of Colorado Cancer Center, Division of Medical Oncology, Department of Medicine.
Elizabeth Molina KunaUniversity of Colorado Cancer Center, Population Health Shared Resource.
Tyler P RobinUniversity of Colorado Cancer Center, Department of Radiation Oncology.
Boris GershmanBeth Israel Deaconess Medical Center, Division of Urologic Surgery.
Thomas W FlaigUniversity of Colorado Cancer Center, Division of Medical Oncology, Department of Medicine.
Simon P KimUniversity of Colorado Cancer Center, Department of Surgery, Division of Urology. Electronic address: simon.kim@cuanschutz.edu.

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
NCI NIH HHS P30 CA046934
6 · The paper itself

Abstract

backgroundIn metastatic hormone-sensitive prostate cancer (mHSPC), androgen deprivation therapy and standard of care treatment intensification with docetaxel and/or an androgen receptor signaling inhibitor (ARSI) are associated with improved survival outcomes for appropriate patients.

methodsThis retrospective study selected patients with de novo mHSPC diagnosed between 2014 and 2023 from CancerLinQ Discovery®, a United States (US)-based, de-identified clinical database. Patient-level data, including clinical characteristics, treatments, and demographics, were collected from CancerLinQ. Treatment intensification was defined as the use of docetaxel, abiraterone, apalutamide, enzalutamide, or docetaxel plus abiraterone or darolutamide. Patient characteristics and treatment intensification data were analyzed descriptively and using multivariable logistic regression.

resultsOf the 3,684 patients with mHSPC, the overall rate of treatment intensification was 58.4% but increased from 32.5% in 2014 to 67.5% in 2023. A relative decline in docetaxel use was accompanied by an increase in ARSI use. Black patients with mHSPC were less likely to receive treatment identification (OR 0.78, 95% CI 0.64-0.95, P = 0.013). Treatment intensification was also less likely for patients of older age and increased ECOG performance status. Despite increasing treatment intensification for Black patients with mHSPC over time, rates of docetaxel use are disproportionately declining relative to White patients.

conclusionsTreatment intensification rates are increasing to include the majority of patients with mHSPC. However, treatment disparities exist for Black patients, who are less likely to receive intensification. These findings illustrate the importance of promoting treatment intensification in appropriate patients and addressing racial treatment disparities.

Indexed as

DocetaxelPractice Patterns, Physicians'Prostatic NeoplasmsAgedAged, 80 and overAndrogen AntagonistsAndrogen Receptor AntagonistsAndrostenesAntineoplastic Combined Chemotherapy ProtocolsBenzamidesDatabases, FactualHumansMaleMiddle AgedNitrilesPhenylthiohydantoinabirateroneAndrogen AntagonistsAndrogen Receptor AntagonistsAndrostenesapalutamideBenzamidesdarolutamideDocetaxelenzalutamideNitrilesPhenylthiohydantoinPyrazolesThiohydantoinsandrogen deprivation therapyandrogen receptor signaling inhibitorsdocetaxelracial disparities

Identifiers

PMID39191549
PMCPMC11573622

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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.