Evidence map›Paper›PMID 40439959›Full record

ArticleAdvances in therapy2025

Overall Survival with Apalutamide Versus Enzalutamide in Metastatic Castration-Sensitive Prostate Cancer.

Mehmet A Bilen, Benjamin Lowentritt, Ibrahim Khilfeh, Carmine Rossi, Shawn Du, Frederic Kinkead, Lilian Diaz, Dominic Pilon, Lorie Ellis, Neal D Shore

Abstract readComparative Study
In one paragraph

Article in Advances in therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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

10 authors.

Mehmet A BilenWinship Cancer Institute of Emory University, Atlanta, GA, USA.
Benjamin LowentrittChesapeake Urology, Towson, MD, USA.
Ibrahim KhilfehJohnson & Johnson, Horsham, PA, USA.
Carmine RossiAnalysis Group, Inc., Montréal, QC, Canada.
Shawn DuJohnson & Johnson, Horsham, PA, USA.
Frederic KinkeadAnalysis Group, Inc., Montréal, QC, Canada.
Lilian DiazAnalysis Group, Inc., Montréal, QC, Canada.
Dominic PilonAnalysis Group, Inc., Montréal, QC, Canada.
Lorie EllisJohnson & Johnson, Horsham, PA, USA.
Neal D ShoreSTART Carolinas/Carolina Urologic Research Center, 823 82nd Parkway, Myrtle Beach, SC, 29572, USA. nshore@auclinics.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSurvival outcomes associated with different androgen receptor pathway inhibitors (ARPIs) prescribed for the treatment of metastatic castration (hormone)-sensitive prostate cancer (mCSPC) have not been directly compared. The objective of this study was to compare overall survival (OS) by 24 months among ARPI-naïve patients with mCSPC initiating apalutamide or enzalutamide.

methodsA retrospective, causal longitudinal inverse probability of treatment weighted analysis was conducted to compare OS between patients initiating apalutamide or enzalutamide between December 2019 and December 2023 using de-identified linked US clinical and insurance claims data. Patients were excluded if they had prior exposure to ARPIs, had evidence of castration resistance, had < 12 months of database activity prior to ARPI initiation, were diagnosed with other primary cancers, or were treated with other advanced prostate cancer (PC)-related treatment (except docetaxel). Using an intention-to-treat approach, weighted Cox proportional hazards models were used to compare OS by 24 months between patients treated with apalutamide or enzalutamide (primary analyses; exploratory analyses used all available follow-up).

resultsOverall, 1810 and 1909 ARPI-naïve patients who initiated apalutamide or enzalutamide, respectively, were included. Measured baseline characteristics between cohorts were well balanced after weighting (for both: mean age 73.0 years, ~ 60% white, ~ 23% black or African American, ~ 78% Medicare-insured, mean Quan-CCI 8.6, ~ 20% with visceral metastasis, 56.2% with de novo PC). At 24 months post index, there was a statistically significant 23% reduction in the risk of mortality among patients who initiated apalutamide compared with enzalutamide (hazard ratio [HR] 0.77; 95% confidence interval [CI] 0.62, 0.96; p = 0.019). Results remained consistent when using all available follow-up metrics (HR 0.77; 95% CI 0.64, 0.93; nominal p = 0.008).

conclusionIn this head-to-head causal analysis among ARPI-naïve patients with mCSPC, treatment with apalutamide resulted in better survival outcomes at 24 months compared with enzalutamide. Longer follow-up studies are required to fully determine the therapeutic comparator impact of these agents.

Indexed as

Androgen Receptor AntagonistsAntineoplastic AgentsBenzamidesNitrilesPhenylthiohydantoinProstatic Neoplasms, Castration-ResistantThiohydantoinsAgedAged, 80 and overHumansMaleMiddle AgedNeoplasm MetastasisRetrospective StudiesAndrogen Receptor AntagonistsAntineoplastic AgentsapalutamideBenzamidesenzalutamideNitrilesPhenylthiohydantoinThiohydantoinsAndrogen receptor pathway inhibitorsComparative effectivenessHormonal antineoplastic agentsHormone-sensitiveProstatic neoplasms

Identifiers

PMID40439959
PMCPMC12182483

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Registered trials

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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.