Evidence map›Paper›PMID 29124881›Full record

ArticleBJU international2018

The implications of baseline bone-health assessment at initiation of androgen-deprivation therapy for prostate cancer.

Peter S Kirk, Tudor Borza, Vahakn B Shahinian, Megan E V Caram, Danil V Makarov, Jeremy B Shelton, John T Leppert, Ryan M Blake, Jennifer A Davis, Brent K Hollenbeck and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in BJU international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Prostate Cancer Surveillance After Radiation Therapy in a National Delivery System.Federal practitioner : for the health care professionals of the VA, DoD, and PHS · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Peter S KirkDow Division of Health Services Research, Department of Urology, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID 0000-0001-7638-8089
Tudor BorzaDow Division of Health Services Research, Department of Urology, University of Michigan Medical School, Ann Arbor, MI, USA.
Vahakn B ShahinianDivision of Nephrology, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
Megan E V CaramDivision of Hematology and Oncology, Department of Internal Medicine, University of Michigan Health System, University of Michigan Medical School, Ann Arbor, MI, USA.
Danil V MakarovDepartments of Urology and Population Health, NYU Langone Medical Center, New York City, NY, USA.
Jeremy B SheltonVA Greater Los Angeles Healthcare System, Los Angeles City, LA, USA.
John T LeppertDepartment of Urology, Stanford University School of Medicine, Stanford, CA, USA.
Ryan M BlakeDow Division of Health Services Research, Department of Urology, University of Michigan Medical School, Ann Arbor, MI, USA.
Jennifer A DavisVeterans Affairs (VA) Health Services Research and Development, Center for Clinical Management Research, VA Ann Arbor Healthcare System, University of Michigan Medical School, Ann Arbor, MI, USA.
Brent K HollenbeckDow Division of Health Services Research, Department of Urology, University of Michigan Medical School, Ann Arbor, MI, USA.
Anne SalesVeterans Affairs (VA) Health Services Research and Development, Center for Clinical Management Research, VA Ann Arbor Healthcare System, University of Michigan Medical School, Ann Arbor, MI, USA.
Ted A SkolarusDow Division of Health Services Research, Department of Urology, University of Michigan Medical School, Ann Arbor, MI, USA.
University of Michigan · USNYU Langone Health · USVA Greater Los Angeles Healthcare System · USVA Palo Alto Health Care System · US

Funding

Advanced Training in Urologic OncologyT32CA180984 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Ganesh S Palapattu, VAHAKN B SHAHINIAN · 2014 to 2026
$3.4M
Major surgery in patients with Alzheimer's disease and related dementias: effects of technology and policyR01AG048071 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOLLENBECK, BRENT K. · 2015 to 2019
$3.0M
Michigan Institute for Clinical and Health Research (MCHR)TL1TR000435 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$1.8M
Impact of urologist practice organization and health policy on prostate cancer treatment, overtreatment and spendingR01HS025707 · AHRQ · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOLLENBECK, BRENT K., SHAHINIAN, VAHAKN B · 2017 to 2021
$1.7M
Improving the prostate cancer survivorship care of veteransIK2HX001162 · VA · VETERANS HEALTH ADMINISTRATION · PI SKOLARUS, TED ALBERT · 2015 to 2018
–
AHRQ HHS R01 HS025707HSRD VA IK2 HX001162NCATS NIH HHS TL1 TR000435NCI NIH HHS T32 CA180984NIA NIH HHS R01 AG048071
6 · The paper itself

Abstract

objectivesTo assess bone-density testing (BDT) use amongst prostate cancer survivors receiving androgen-deprivation therapy (ADT), and downstream implications for osteoporosis and fracture diagnoses, as well as pharmacological osteoporosis treatment in a national integrated delivery system. PATIENTS AND

methodsWe identified 17 017 men with prostate cancer who received any ADT between 2005 and 2014 using the Veterans Health Administration cancer registry and administrative data. We identified claims for BDT within a 3-year period of ADT initiation. We then used multivariable regression to examine the association between BDT use and incident osteoporosis, fracture, and use of pharmacological treatment.

resultsWe found that a minority of patients received BDT (n = 2 502, 15%); however, the rate of testing increased to >20% by the end of the study period. Men receiving BDT were older at diagnosis and had higher-risk prostate cancer (both P < 0.001). Osteoporosis and fracture diagnoses, use of vitamin D ± calcium, and bisphosphonates were all more common in men who received BDT. After adjustment, BDT, and to a lesser degree ≥2 years of ADT, were both independently associated with incident osteoporosis, fracture, and osteoporosis treatment.

conclusionsBDT is rare amongst patients with prostate cancer treated with ADT in this integrated delivery system. However, BDT was associated with substantially increased treatment of osteoporosis indicating an underappreciated burden of osteoporosis amongst prostate cancer survivors initiating ADT. Optimising BDT use and osteoporosis management in this at-risk population appears warranted.

Indexed as

Androgen AntagonistsFractures, BoneOsteoporosisProstatic NeoplasmsAgedBone DensityHumansMaleMiddle AgedRetrospective StudiesAndrogen Antagonistsanti-androgen effectbonebone densityfracturesosteoporosis#PCSM#ProstateCancerprostatic neoplasms

Identifiers

PMID29124881
PMCPMC5878705
OpenAlexW2768058331

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.