Evidence map›Paper›PMID 31584456›Full record

ArticleAmerican journal of clinical oncology2019

Definitive Radiation Treatment Patterns and Outcomes for Low and Intermediate Risk Prostate Cancer Patients: A Cross-Continental Comparative Study.

Francis A Asamoah, Joel Yarney, Shivanshu Awasthi, Verna Vanderpuye, Mary A Dadzie, Angelina Fink, Arash O Naghavi, Afua Abrahams, James E Mensah, Evans Sasu and 4 more

Abstract readComparative Study
In one paragraph

Article in American journal of clinical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

14 authors.

Francis A AsamoahNational Center for Radiotherapy, Oncology and Nuclear Medicine (NCRONM).
Joel YarneyNational Center for Radiotherapy, Oncology and Nuclear Medicine (NCRONM).
Shivanshu AwasthiCancer Epidemiology.
Verna VanderpuyeNational Center for Radiotherapy, Oncology and Nuclear Medicine (NCRONM).
Mary A DadzieNational Center for Radiotherapy, Oncology and Nuclear Medicine (NCRONM).
Angelina FinkCancer Epidemiology.
Arash O NaghaviDepartments of Radiation Oncology.
Afua AbrahamsDepartment of Pathology.
James E MensahDepartment of Surgery, Korle Bu Teaching Hospital Accra, Ghana, West Africa.
Evans SasuNational Center for Radiotherapy, Oncology and Nuclear Medicine (NCRONM).
Samuel N TagoeNational Center for Radiotherapy, Oncology and Nuclear Medicine (NCRONM).
Jasreman DhillonPathology H. Lee Moffitt Cancer Center, Tampa, FL.
Peter A S JohnstoneDepartments of Radiation Oncology.
Kosj YamoahDepartments of Radiation Oncology.

Funding

Precision Interception of Aggressive Prostate Cancer in African American MenP20CA233255 · NCI · DANA-FARBER CANCER INST · PI REBBECK, TIMOTHY R · 2018 to 2020
$3.2M
NCI NIH HHS P20 CA233255
6 · The paper itself

Abstract

purposeTo evaluate early-stage prostate cancer (PCa) radiotherapy treatment patterns and outcomes among Ghanaian men (GM) compared with US men (USM). MATERIALS AND

methodsThis retrospective study consists of 987 National Comprehensive Cancer Network low risk, favorable intermediate risk, and unfavorable intermediate risk PCa patient subgroups; GM (173) and USM (814). Differences in baseline covariates and clinical characteristics between GM and USM were analyzed using χ and Mann-Whitney test while Cox Proportional Hazards model was used to assess freedom from biochemical failure differences between the study groups.

resultsMedian follow-up for this study was 40 months. GM were diagnosed at a younger median age (64 vs. 68 y, P<0.001) with heavier unfavorable intermediate risk disease burden (32.4% vs. 19.2%) compared with USM. Significant differences were identified in median external beam radiotherapy dose (72.4 vs. 78 Gy, P<0.001); brachytherapy utilization (49.7% vs. 80.6%, P<0.001) and androgen deprivation therapy for intermediate risk disease (48.4% vs. 21.0%, P<0.001) between GM and USM, respectively. GM with low risk and favorable intermediate risk PCa were at increased risk of biochemical recurrence compared with USM with adjusted hazard ratio: 5.15 (1.27 to 20.7), P=0.02 and 4.64 (1.20 to 17.92), P=0.02, respectively.

conclusionsCompared with USM, GM with low and favorable intermediate risk PCa may experience less durable disease control following standard treatment recommendations. Results suggest differences in radiation treatment and possible inherent differences between the 2 populations. This data will aid in developing research strategies to improve treatment outcomes in GM.

Indexed as

Cause of DeathAgedAge FactorsAndrogen AntagonistsBrachytherapyCohort StudiesDisease-Free SurvivalGhanaHospitals, TeachingHumansMaleMiddle AgedNeoplasm InvasivenessNeoplasm StagingProportional Hazards ModelsProstatic NeoplasmsAndrogen Antagonists

Identifiers

PMID31584456
PMCPMC6887629

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.