Evidence map›Paper›PMID 32807727›Full record

Trial reportEuropean urology oncology2020

Patterns of Cancer Progression of Metastatic Hormone-sensitive Prostate Cancer in the ECOG3805 CHAARTED Trial.

Alan H Bryce, Yu Hui Chen, Glenn Liu, Michael A Carducci, David M Jarrard, Jorge A Garcia, Robert Dreicer, Maha Hussain, Mario Alfredo Eisenberger, Elizabeth R Plimack and 4 more

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in European urology oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 37 citations in OpenAlex.

  1. Radiographic Progression With and Without Prostate-Specific Antigen Rise in Patients With Advanced Prostate Cancer Treated With Enzalutamide.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
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  17. Liquid biopsy to personalize treatment for metastatic prostate cancer.American journal of translational research · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 10 institutions in 1 country.

Alan H BryceDivision of Hematology and Medical Oncology, Mayo Clinic, Phoenix, AZ, USA. Electronic address: Bryce.alan@mayo.edu.
Yu Hui ChenDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
Glenn LiuCarbone Cancer Center, University of Wisconsin, Madison, WI, USA.
Michael A CarducciDepartment of Oncology, Johns Hopkins University, Baltimore, MD, USA.
David M JarrardDepartment of Urology, University of Wisconsin, Madison, WI, USA.
Jorge A GarciaDepartment of Medicine, Case Comprehensive Cancer Center, Cleveland, OH, USA.
Robert DreicerNevada Cancer Research Foundation, Las Vegas, NV, USA.
Maha HussainDivision of Hematology Oncology, Northwestern University, Chicago, IL, USA.
Mario Alfredo EisenbergerDepartment of Urology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Elizabeth R PlimackDepartment of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA.
Nicholas J VogelzangNevada Cancer Research Foundation, Las Vegas, NV, USA.
Robert S DiPaolaCollege of Medicine, University of Kentucky, Lexington, KY, USA.
Lauren HarshmanDepartment of Medicine, Dana-Farber Cancer Institute, Boston, MA, USA.
Christopher J SweeneyDivision of Hematology/Oncology, University of Virginia Cancer Center, USA.
Dana-Farber Cancer Institute · USJohns Hopkins University · USNevada Cancer Research Foundation · USUniversity of Wisconsin–Madison · USCase Comprehensive Cancer CenterFox Chase Cancer Center · USMayo Clinic in Arizona · USNorthwestern University · USUniversity of Kentucky · USUniversity of Virginia Cancer Center

Funding

Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Project-006U10CA180820 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer, MITCHELL D. SCHNALL · 2014 to 2026
$167.6M
SWOG Network Group Operations Center of the NCTNU10CA180888 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PRIMO N. LARA · 2014 to 2026
$152.1M
Statistics CoreU10CA180794 · NCI · DANA-FARBER CANCER INST · PI PAUL J CATALANO, CONSTANTINE A. GATSONIS · 2014 to 2026
$111.2M
Nevada Cancer Research Foundation-NCI Community Oncology Research ProgramUG1CA189829 · NCI · SOUTHERN NEVADA CANCER RESEARCH FDN · PI Khawaja Saad Jahangir, Joseph Louis Lasky · 2014 to 2026
$14.7M
Case Comprehensive Cancer Center NCTN Lead Academic Participating SiteUG1CA233234 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI Aaron Thomas Gerds, Daniel Eidelberg Spratt · 2019 to 2026
$11.1M
NCTN Lead Academic Participating Site at Dana-Farber/Partners Cancer CareUG1CA233180 · NCI · DANA-FARBER CANCER INST · PI Harold John Burstein · 2019 to 2026
$8.6M
NCI, National Clinical Trials Network Lead Academic Participating Site (LAPS) UG1 (funded extension)UG1CA232760 · NCI · MAYO CLINIC ROCHESTER · PI Judy Caroline Boughey, Aaron Scott Mansfield · 2019 to 2026
$8.5M
Washington University/ Siteman Cancer Center Lead Academic SiteU10CA180833 · NCI · WASHINGTON UNIVERSITY · PI BARTLETT, NANCY L, KOZOWER, BENJAMIN D · 2014 to 2018
$7.6M
Naional Cancer Institute, Naitonal Clinical Trials Network U10 Lead Academic SiteU10CA180790 · NCI · MAYO CLINIC ROCHESTER · PI ALBERTS, STEVEN R, BOUGHEY, JUDY CAROLINE · 2014 to 2018
$6.6M
CWRU Case Comprehensive Cancer Center NCTN Lead Academic Participating SiteU10CA180853 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI GERDS, AARON THOMAS, MACHTAY, MITCHELL · 2014 to 2018
$6.2M
NCTN Lead Academic Participating Site at Dana-Farber/Partners Cancer CareU10CA180867 · NCI · DANA-FARBER CANCER INST · PI BURSTEIN, HAROLD JOHN, KIBEL, ADAM S · 2014 to 2018
$6.2M
NCI NIH HHS U10 CA180790NCI NIH HHS U10 CA180794NCI NIH HHS U10 CA180795NCI NIH HHS U10 CA180799NCI NIH HHS U10 CA180801NCI NIH HHS U10 CA180802NCI NIH HHS U10 CA180820NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180833NCI NIH HHS U10 CA180853NCI NIH HHS U10 CA180867NCI NIH HHS U10 CA180888NCI NIH HHS UG1 CA189829NCI NIH HHS UG1 CA232760NCI NIH HHS UG1 CA233180NCI NIH HHS UG1 CA233196NCI NIH HHS UG1 CA233234NCI NIH HHS UG1 CA233277NCI NIH HHS UG1 CA233320
6 · The paper itself

Abstract

backgroundECOG3805 is a randomized trial of testosterone suppression with or without docetaxel for metastatic hormone-sensitive prostate cancer (mHSPC). Deeper prostate-specific antigen (PSA) suppression is prognostic for outcome. However, the concordance of PSA rise and radiographic progression has not been examined previously in mHSPC, whereas this has been reported in metastatic castration-resistant prostate cancer.

objectiveTo determine the patterns of progression by PSA and radiographic parameters in patients in ECOG3805. DESIGN, SETTING, AND

participantsWe conducted a retrospective analysis of all patients in ECOG3805. Patients were classified according to the PSA level at progression (whether PSA level was below 2.0 ng/mL or not) and the type of progression event in the study (either PSA progression as defined by the study with or without clinical progression, or clinical progression alone). Baseline demographics, clinical outcomes, and patterns of progression were compared between the groups. RESULTS AND LIMITATIONS: One in eight patients had clinical progression below a PSA level of 2 ng/mL, and approximately 25% developed clinical progression in the absence of confirmed PSA progression. Overall survival from randomization was shorter in patients with clinical progression without confirmed PSA progression than in patients with PSA progression alone as the first progression. Patient demographics at study entry were not predictive of the pattern of progression. Study limitations include its retrospective and post hoc nature.

conclusionsClinical progression prior to PSA rise or at low PSA levels is a relatively frequent phenomenon in mHSPC and is associated with poorer overall survival. Further biological and clinical studies of these patients are warranted. PATIENT SUMMARY: Reliance on prostate-specific antigen (PSA) alone is an inadequate strategy to monitor patients undergoing treatment for metastatic hormone-sensitive prostate cancer. Prostate cancer can get worse on scans even with low PSA and/or no or small changes in PSA. Imaging should be added to PSA testing to monitor patients with metastatic prostate cancer.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Agents, HormonalAntineoplastic Combined Chemotherapy ProtocolsDisease ProgressionDocetaxelGonadotropin-Releasing HormoneHumansKallikreinsMaleMiddle AgedNeoplasm GradingPrognosisProgression-Free SurvivalProspective StudiesAntineoplastic Agents, HormonalDocetaxelGonadotropin-Releasing HormoneKallikreinsKLK3 protein, humanProstate-Specific AntigenTestosteroneChemotherapyClinical trialHormone therapyProstate cancerProstate-specific antigen

Identifiers

PMID32807727
PMCPMC7738423
OpenAlexW3049620688

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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.