Evidence map›Paper›PMID 29475737›Full record

SynthesisEuropean urology2018

Burden of Metastatic Castrate Naive Prostate Cancer Patients, to Identify Men More Likely to Benefit from Early Docetaxel: Further Analyses of CHAARTED and GETUG-AFU15 Studies.

Gwenaelle Gravis, Jean-Marie Boher, Yu-Hui Chen, Glenn Liu, Karim Fizazi, Michael A Carducci, Stephane Oudard, Florence Joly, David M Jarrard, Michel Soulie and 10 more

Open access · greenAbstract readMeta-Analysis
In one paragraph

Synthesis in European urology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 8 pooled it
21.8field-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.

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

101 citing papers in PubMed, 8 syntheses or guidelines pooled it, 246 citations in OpenAlex.

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  9. [Molecular imaging and biology · 2025
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  11. Orteronel for Metastatic Hormone-Sensitive Prostate Cancer: A Multicenter, Randomized, Open-Label Phase III Trial (SWOG-1216).Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
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41 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 16 institutions in 2 countries.

Gwenaelle GravisCentre de Recherche en Cancerologie de Marseille (CRCM), Institut Paoli-Calmettes, Aix-Marseille University, Marseille, France. Electronic address: gravisg@ipc.unicancer.fr.
Jean-Marie BoherBiostatistic, Institut Paoli-Calmettes, Aix-Marseille Universite, Marseille, France.
Yu-Hui ChenDana-Farber Cancer Institute, ECOG-ACRIN Biostatistics Center, Boston, MA, USA.
Glenn LiuUniversity of Wisconsin Carbone Cancer Center, Madison, WI, USA.
Karim FizaziGustave Roussy, University of Paris Sud, Villejuif, France.
Michael A CarducciJohns Hopkins University, Baltimore, MD, USA.
Stephane OudardDepartment of Medical Oncology, Hopital Europeen Georges Pompidou, Paris, France.
Florence JolyCentre Francois Baclesse, Caen, France.
David M JarrardUniversity of Wisconsin Carbone Cancer Center, Madison, WI, USA.
Michel SoulieCentre Hospitalier Universitaire Rangueil, Toulouse, France.
Mario J EisenbergerJohns Hopkins University, Baltimore, MD, USA.
Muriel HabibianUNICANCER, Paris, France.
Robert DreicerUniversity of Virginia, Charlottesville, VA, USA.
Jorge A GarciaCleveland Clinic Foundation, Cleveland, OH, USA.
Maha H M HussainUniversity of Michigan Comprehensive Cancer, Ann Arbor, MI, USA.
Manish KohliMayo Clinic, Rochester, MN, USA.
Nicholas J VogelzangNevada Cancer Research Foundation, Las Vegas, NV, USA.
Joel PicusWashington University School of Medicine, St. Louis, MO, USA.
Robert DiPaolaUniversity of Kentucky College of Medicine, Lexington, KY, USA.
Christopher SweeneyDana-Farber Cancer Institute, Boston, MA, USA.
Aix-Marseille Université · FRDana-Farber Cancer Institute · USJohns Hopkins University · USUniversity of Wisconsin Carbone Cancer Center · USCentre François Baclesse · FRCentre Hospitalier Universitaire de Toulouse · FRCleveland Clinic · USHôpital Européen Georges-Pompidou · FRMayo Clinic in Arizona · USNevada Cancer Research Foundation · USUniCancer Group · FRUniversité Paris-Sud · FRUniversity of Kentucky · USUniversity of Michigan–Ann Arbor · USUniversity of Virginia · USWashington University in St. Louis · US

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
CANCER AND LEUKEMIA GROUP B MINORITY SATELLITE SUPPLEMENU10CA031946 · NCI · UNIVERSITY OF CHICAGO · PI BERTAGNOLLI, MONICA M · 1985 to 2013
$158.4M
SWOG Network Group Operations Center of the NCTNU10CA180888 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PRIMO N. LARA · 2014 to 2026
$152.1M
SWOG - Foreign Accrual under UMiU10CA032102 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BLANKE, CHARLES D. · 1985 to 2013
$141.3M
ECOG OPERATIONS OFFICE (IBCSG)U10CA021115 · NCI · UNIVERSITY OF WISCONSIN MADISON · PI COMIS, ROBERT L · 1985 to 2013
$132.6M
Statistics CoreU10CA180794 · NCI · DANA-FARBER CANCER INST · PI PAUL J CATALANO, CONSTANTINE A. GATSONIS · 2014 to 2026
$111.2M
ECOG Statistical Office Data Management GrantU10CA066636 · NCI · FRONTIER SCI &TECHNOLOGY RSCH FDN, INC · PI GRAY, ROBERT J · 1994 to 2013
$39.5M
PROVIDE STATISTICAL SERVICESU10CA023318 · NCI · DANA-FARBER CANCER INSTITUTE · PI GRAY, ROBERT J · 1985 to 2013
$33.4M
Targeting FOXA1-downstream pathways: a novel therapeutic strategy for castration-resistant prostate cancerP50CA180995 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A., HUSSAIN, MAHA H · 2015 to 2025
$19.9M
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
SOUTHERN NEVADA CANCER RESEARCH FOUNDATION-CCOPU10CA035421 · NCI · SOUTHERN NEVADA CANCER RESEARCH FDN · PI ELLERTON, JOHN A · 1985 to 2014
$9.8M
NCI NIH HHS N01 CA004919NCI NIH HHS N01 CA032102NCI NIH HHS P50 CA180995NCI NIH HHS U10 CA004919NCI NIH HHS U10 CA013650NCI NIH HHS U10 CA014548NCI NIH HHS U10 CA016116NCI NIH HHS U10 CA021076NCI NIH HHS U10 CA021115NCI NIH HHS U10 CA023318NCI NIH HHS U10 CA027525NCI NIH HHS U10 CA031946NCI NIH HHS U10 CA032102NCI NIH HHS U10 CA035421NCI NIH HHS U10 CA049883NCI NIH HHS U10 CA066636NCI NIH HHS U10 CA107868NCI NIH HHS U10 CA180790NCI NIH HHS U10 CA180794NCI 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 CA180847NCI NIH HHS U10 CA180853NCI NIH HHS U10 CA180867NCI NIH HHS U10 CA180888NCI NIH HHS UG1 CA189829NCI NIH HHS UG1 CA232760NCI NIH HHS UG1 CA233196
6 · The paper itself

Abstract

backgroundDocetaxel (D) at the time of starting androgen deprivation therapy (ADT) for metastatic castrate naive prostate cancer shows a clear survival benefit for patients with high-volume (HV) disease. It is unclear whether patients with low-volume (LV) disease benefit from early D.

objectiveTo define the overall survival (OS) of aggregate data of patient subgroups from the CHAARTED and GETUG-AFU15 studies, defined by metastatic burden (HV and LV) and time of metastasis occurrence (at diagnosis or after prior local treatment [PRLT]). DESIGN, SETTING, AND

participantsData were accessed from two independent phase III trials of ADT alone or ADT+D-GETUG-AFU15 (N=385) and CHAARTED (N=790), with median follow-ups for survivors of 83.2 and 48.2 mo, respectively. The definition of HV and LV disease was harmonized. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: The primary end point was OS. RESULTS AND LIMITATIONS: Meta-analysis results of the aggregate data showed significant heterogeneity in ADT+D versus ADT effect sizes between HV and LV subgroups (p=0.017), and failed to detect heterogeneity in ADT+D versus ADT effect sizes between upfront and PRLT subgroups (p=0.4). Adding D in patients with HV disease has a consistent effect in improving median OS (HV-ADT: 34.4 and 35.1 mo, HV-ADT+D: 51.2 and 39.8 mo in CHAARTED and GETUG-AFU15, respectively; pooled average hazard ratio or HR (95% confidence interval [CI]) 0.68 ([95% CI 0.56; 0.82], p<0.001). Patients with LV disease showed much longer OS, without evidence that D improved OS (LV-ADT: not reached [NR] and 83.4; LV-ADT+D: 63.5 and NR in CHAARTED and GETUG-AFU15, respectively; pooled HR (95% CI) 1.03 (95% CI 0.77; 1.38). Aggregate data showed no evidence of heterogeneity of early D in LV and HV subgroups irrespective of whether patients had PRLT or not. Post hoc subgroup analysis was based on aggregated data from two independent phase III randomized trials.

conclusionsThere was no apparent survival benefit in the CHAARTED and GETUG-AFU15 studies with D for LV. Across both studies, early D showed consistent effect and improved OS in HV patients. PATIENT SUMMARY: Patients with a higher burden of metastatic prostate cancer starting androgen deprivation therapy (ADT) have a poorer prognosis and are more likely to benefit from early docetaxel. Low-volume patients have longer overall survival with ADT alone, and the toxicity of docetaxel may outweigh its benefits.

Indexed as

Tumor BurdenAgedAndrogen AntagonistsAntineoplastic Combined Chemotherapy ProtocolsBone NeoplasmsClinical Trials, Phase III as TopicDocetaxelGonadotropin-Releasing HormoneHumansMaleMiddle AgedNeoplasm MetastasisOrchiectomyPrognosisProstatic NeoplasmsRandomized Controlled Trials as TopicAndrogen AntagonistsDocetaxelGonadotropin-Releasing HormoneAndrogen deprivation therapyChemotherapyDocetaxelHigh volumeLow volumeMetastatic castrate naive prostate cancerMetastatic prostate cancerProstate cancerVolume disease

Identifiers

PMID29475737
PMCPMC6010352
OpenAlexW2788841415

What OpenQuestion holds

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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.