Evidence map›Paper›PMID 35123889›Full record

ArticleBrachytherapy

Assessing the role of external beam radiation therapy in combination with brachytherapy versus brachytherapy alone for unfavorable intermediate-risk prostate cancer.

Neal Andruska, Jeff M Michalski, Ruben Carmona, Temitope Agabalogun, Randall J Brenneman, Hiram A Gay, Benjamin W Fischer-Valuck, Brian C Baumann

Open access · greenAbstract read
In one paragraph

Article in Brachytherapy. 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
0.2field-weighted citation impact, top 55% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

8 authors at 4 institutions in 1 country.

Neal AndruskaDepartment of Radiation Oncology, Siteman Cancer Center, Washington University School of Medicine, Saint Louis, MO. Electronic address: andruska.neal@wustl.edu.
Jeff M MichalskiDepartment of Radiation Oncology, Siteman Cancer Center, Washington University School of Medicine, Saint Louis, MO.
Ruben CarmonaDepartment of Radiation Oncology, Sylvester Cancer Center, University of Miami, Miami, FL.
Temitope AgabalogunDepartment of Radiation Oncology, Siteman Cancer Center, Washington University School of Medicine, Saint Louis, MO.
Randall J BrennemanDepartment of Radiation Oncology, Siteman Cancer Center, Washington University School of Medicine, Saint Louis, MO.
Hiram A GayDepartment of Radiation Oncology, Siteman Cancer Center, Washington University School of Medicine, Saint Louis, MO.
Benjamin W Fischer-ValuckDepartment of Radiation Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA.
Brian C BaumannDepartment of Radiation Oncology, Siteman Cancer Center, Washington University School of Medicine, Saint Louis, MO; Department of Radiation Oncology, Abramson Cancer Center, University of Pennsylvania School of Medicine, Philadelphia, PA. Electronic address: brian.baumann@wustl.edu.
Washington University in St. Louis · USEmory University · USUniversity of Miami · USUniversity of Pennsylvania · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
NCI NIH HHS P30 CA091842
6 · The paper itself

Abstract

backgroundDefinitive treatment options for unfavorable intermediate-risk prostate cancer (UIR-PCa) include external beam radiotherapy (EBRT) ± brachytherapy boost ± androgen deprivation therapy (ADT). The role of brachytherapy ± ADT in the absence of EBRT is not well defined. We hypothesized that EBRT+BT±ADT is associated with improved overall survival (OS) relative to BT±ADT for UIR-PCa. METHODS AND MATERIALS: Men with UIR-PCa diagnosed between 2004 and 2015 were identified in the National Cancer Database (NCDB). Inverse propensity of treatment weighting was used to balance covariables that influenced treatment allocation and outcomes, and propensity-weighted multivariable analysis (MVA) using Cox regression modeling was used to compare OS hazard ratios.

resultsA total of 11,721 men were stratified into four treatment groups: (1) BT without ADT (n = 4,535), (2) BT+ADT (n = 1,303), (3) EBRT+BT (n = 3,446), or (4) EBRT+BT+ADT (n = 2,437). Relative to patients treated with BT alone, BT+ADT (Hazard Ratio (HR): 0.86 [95% Confidence Interval (CI): 0.76-0.99], p = 0.03), EBRT+BT (HR: 0.79 [0.70-0.88], p = 0.00002), and EBRT+BT+ADT (HR: 0.76 [0.67-0.85], p = 0.000003) were associated with improved OS on MVA. Relative to BT alone, EBRT+BT correlated with improved OS on weight-adjusted MVA (HR: 0.82 [0.75-0.89], p = 0.000005). 10-year OS for BT vs. EBRT+BT was 62.4% [60.1-64.7] vs. 69.3% [67.5-71.2], respectively (p < 0.0001).

conclusionsEBRT+BT correlated with improved OS relative to BT alone in men with UIR-PCa, reaffirming current NCCN recommendations recommending EBRT+BT over BT alone. While prior studies reported no benefit to adding EBRT to BT with optimal implant dosimetry, this study suggests men benefit from EBRT in a population of variable implant quality.

Indexed as

BrachytherapyProstatic NeoplasmsAndrogen AntagonistsHumansMaleProportional Hazards ModelsRetrospective StudiesAndrogen AntagonistsBrachytherapyIntermediate-riskProstate cancerRadiation treatmentRadiotherapyUnfavorable intermediate-risk

Identifiers

PMID35123889
PMCPMC9169575
OpenAlexW4210426956

What OpenQuestion holds

Textmetadata
LicenceTDM
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.