Evidence map›Paper›PMID 26720308›Full record

Trial reportJAMA oncology2016

Adverse Health Events Following Intermittent and Continuous Androgen Deprivation in Patients With Metastatic Prostate Cancer.

Dawn L Hershman, Joseph M Unger, Jason D Wright, Scott Ramsey, Cathee Till, Catherine M Tangen, William E Barlow, Charles Blanke, Ian M Thompson, Maha Hussain

2 registry-linked trialsOpen access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 49 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 3 pooled it
9.3field-weighted citation impact, top 1% 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.

NCT00002651 phase3completednot on this map

Intermittent Androgen Deprivation in Patients With Stage D2 Prostate Cancer, Phase III

TypeinterventionalSponsorSWOG Cancer Research NetworkRan1995 to 2013Enrolled3,040ConditionsProstate CancerArmsbicalutamide, goserelin acetate, clinical observation
NCT02867020 phase2completednot on this mapstarted 2017, after this paper: background citation

Phase II Randomized Study of Abiraterone Acetate Plus ADT Versus APALUTAMIDE Versus Abiraterone and APALUTAMIDE in Patients With Advanced Prostate Cancer With Non-castrate Testosterone Levels

TypeinterventionalSponsorLatin American Cooperative Oncology GroupRan2017 to 2021Enrolled128ConditionsProstate CancerArmsApalutamide, Abiraterone, ADT, Prednisone
3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 3 syntheses or guidelines pooled it, 93 citations in OpenAlex.

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  15. Prostate cancer treatment and the relationship of androgen deprivation therapy to cognitive function.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Dawn L HershmanColumbia University Medical Center, New York, New York.
Joseph M UngerFred Hutchinson Cancer Research Center, Seattle, Washington.
Jason D WrightColumbia University Medical Center, New York, New York.
Scott RamseyFred Hutchinson Cancer Research Center, Seattle, Washington.
Cathee TillFred Hutchinson Cancer Research Center, Seattle, Washington.
Catherine M TangenFred Hutchinson Cancer Research Center, Seattle, Washington.
William E BarlowSWOG Statistical Center, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Charles BlankeKnight Cancer Institute, Oregon Health and Science University, Portland.
Ian M ThompsonCancer Therapy and Research Center, San Antonio, Texas.
Maha HussainUniversity of Michigan Comprehensive Cancer Center, Ann Arbor.
Fred Hutch Cancer Center · USColumbia University Irving Medical Center · USOregon Health & Science University · USUniversity of Michigan–Ann Arbor · US

Funding

SWOG Statistics & Data Management Center complex - extension supplement for GY06U10CA180819 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Catherine M. Tangen · 2014 to 2026
$115.2M
SWOG NCORP Research BaseUG1CA189974 · NCI · THE HOPE FOUNDATION · PI CHARLES D. BLANKE, DAWN HERSHMAN · 2014 to 2026
$80.6M
UM LAPs- U10 GrantU10CA180801 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZALUPSKI, MARK M · 2014 to 2018
$3.7M
The Influence of Hospital Variability on the Management of Cancer-Associated CompR01CA169121 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WRIGHT, JASON · 2013 to 2017
$1.8M
Using SWOG-Medicare database to evaluate long-term toxicities of cancer survivorsR01CA166084 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HERSHMAN, DAWN · 2013 to 2016
$1.3M
Determinants and risks of use and overuse of expensive oncology drugsR01CA134964 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HERSHMAN, DAWN · 2008 to 2011
$1.0M
NCI NIH HHS 1UG1CA189974-01NCI NIH HHS R01 CA134964NCI NIH HHS R01CA134964NCI NIH HHS R01 CA166084NCI NIH HHS R01 CA169121NCI NIH HHS R01CA169121-01A1NCI NIH HHS U10 CA180801NCI NIH HHS U10 CA180819NCI NIH HHS UG1 CA189974
6 · The paper itself

Abstract

importanceAlthough intermittent androgen-deprivation therapy (ADT) has not been associated with better overall survival in prostate cancer (PC), it has the potential for lower adverse effects. To our knowledge, the incidence of long-term adverse health events has not been reported.

objectiveTo examine long-term late events in elderly patients randomized to intermittent or continuous ADT to determine whether late cardiovascular and endocrine events would be lower in patients treated with intermittent ADT. DESIGN, SETTING, AND

participantsThis was a secondary analysis of a multicenter clinical trial using linkage between patient data from S9346, a randomized SWOG trial of intermittent vs continuous ADT in men with metastatic PC, and corresponding Medicare claims. EXPOSURE: Intermittent or continuous ADT. MAIN OUTCOMES AND MEASURES: The main outcome was to identify long-term adverse health events by treatment arm. Patients were classified as having an adverse health event if they had any hospital claim--or at least 2 physician or outpatient claims at least 30 days apart--for any of the following diagnoses: ischemic and thrombotic events, endocrine events, sexual dysfunction, dementia, and depression. To incorporate time from beginning of observation through evidence of an event, we determined the cumulative incidence of each event. Competing risks Cox regression was used, adjusting for covariates.

resultsIn total, 1134 eligible US-based male patients with metastatic PC were randomized to continuous vs intermittent ADT in the S9346 trial. A total of 636 of trial participants (56%) had at least 1 year of continuous Medicare parts A and B coverage and no health maintenance organization participation. The median age was 71.3 years. The most common long-term events were hypercholesterolemia (31%) and osteoporosis (19%). The 10-year cumulative incidence of ischemic and thrombotic events differed by arm; 24% for continuous and 33%for intermittent ADT (hazard ratio, 0.69; P = .02). There were no statistically significant differences by arm in any other adverse health events. CONCLUSIONS AND RELEVANCE: Contrary to our hypothesis that intermittent ADT would reduce long-term health-related events compared with continuous ADT, we found that older men assigned to intermittent ADT had no apparent reduction in bone, endocrine, or cognitive events and an increased incidence of ischemic and thrombotic events.

trial registrationclinicaltrials.gov Identifier: NCT00002651.

Indexed as

AgedAndrogen AntagonistsAntineoplastic Agents, HormonalHumansMaleMiddle AgedNeoplasm MetastasisProportional Hazards ModelsProstatic NeoplasmsAndrogen AntagonistsAntineoplastic Agents, Hormonal

Identifiers

PMID26720308
PMCPMC4852142
OpenAlexW2208340908

What OpenQuestion holds

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Registered trials

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.