Evidence map›Paper›PMID 34516663›Full record

ArticleThe Prostate2021

Efficacy of systemic therapies in men with metastatic castration resistant prostate cancer harboring germline ATM versus BRCA2 mutations.

Alexandra O Sokolova, Catherine H Marshall, Rebeca Lozano, Roman Gulati, Elisa M Ledet, Navonil De Sarkar, Petros Grivas, Celestia S Higano, Bruce Montgomery, Peter S Nelson and 10 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in The Prostate, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.1field-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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Metastatic Prostate Cancers with BRCA2 versus ATM Mutations Exhibit Divergent Molecular Features and Clinical Outcomes.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  5. Article
  6. Article
  7. 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

20 authors at 7 institutions in 2 countries.

Alexandra O SokolovaDivision of Medical Oncology, Oregon Health Science University, Portland, Oregon, USA.ORCID 0000-0003-0821-6503
Catherine H MarshallDivision on Medical Oncology, Johns Hopkins School of Medicine, Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, USA.
Rebeca LozanoProstate Cancer Clinical Research Unit, Division on Medical Oncology, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Roman GulatiFred Hutchinson Cancer Research Center, Seattle, Washington, USA.ORCID 0000-0002-7592-6567
Elisa M LedetSystems Engineering and Operations Research Department, George Mason University, Fairfax, Virginia, USA.ORCID 0000-0003-1230-3255
Navonil De SarkarFred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Petros GrivasFred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Celestia S HiganoFred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Bruce MontgomeryDivision of Medical Oncology, Department of Medicine, University of Washington, Seattle, Washington, USA.
Peter S NelsonFred Hutchinson Cancer Research Center, Seattle, Washington, USA.
David OlmosProstate Cancer Clinical Research Unit, Division on Medical Oncology, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Vadim SokolovSystems Engineering and Operations Research Department, George Mason University, Fairfax, Virginia, USA.
Michael T SchweizerFred Hutchinson Cancer Research Center, Seattle, Washington, USA.ORCID 0000-0002-5510-0661
Todd A YezefskiDivision of Medical Oncology, Department of Medicine, University of Washington, Seattle, Washington, USA.
Evan Y YuFred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Channing J PallerDivision on Medical Oncology, Johns Hopkins School of Medicine, Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, USA.ORCID 0000-0003-3658-1858
Oliver SartorDivision on Medical Oncology, Tulane University School of Medicine, New Orleans, Louisiana, USA.ORCID 0000-0002-8777-7343
Elena CastroProstate Cancer Clinical Research Unit, Division on Medical Oncology, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Emmanuel S AntonarakisDivision on Medical Oncology, Johns Hopkins School of Medicine, Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, USA.ORCID 0000-0003-0031-9655
Heather H ChengFred Hutchinson Cancer Research Center, Seattle, Washington, USA.ORCID 0000-0002-1365-0702
University of Washington Medical Center · USJohns Hopkins University · USSpanish National Cancer Research Centre · ESFred Hutch Cancer Center · USGeorge Mason University · USOregon Health & Science University · USTulane University · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI WILLIAM George NELSON · 1985 to 2026
$208.6M
TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
TRAINING IN CANCER BIOLOGY &TRANSPLANTATIONT32CA009515 · NCI · UNIVERSITY OF WASHINGTON · PI NANCY ELLEN DAVIDSON, Effie W Petersdorf · 1985 to 2026
$16.2M
Statistical modeling to support population and translational cancer researchR50CA221836 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Roman Gulati · 2017 to 2026
$2.0M
NCI NIH HHS P30 CA006973NCI NIH HHS P30 CA015704NCI NIH HHS P50 CA097186NCI NIH HHS R50 CA221836NCI NIH HHS T32 CA009515
6 · The paper itself

Abstract

backgroundAmong men with metastatic prostate cancer, about 10% have germline alterations in DNA damage response genes. Most studies have examined BRCA2 alone or an aggregate of BRCA1/2 and ATM. Emerging data suggest that ATM mutations may have distinct biology and warrant individual evaluation. The objective of this study is to determine whether response to prostate cancer systemic therapies differs between men with germline mutations in ATM (gATM) and BRCA2 (gBRCA2).

methodsThis is an international multicenter retrospective matched cohort study of men with prostate cancer harboring gATM or gBRCA2. PSA RESULTS AND LIMITATIONS: The study included 45 gATM and 45 gBRCA2 patients, matched on stage and year of germline testing. Patients with gATM and gBRCA2 had similar age, Gleason grade, and PSA at diagnosis. We did not observe differences in PSA

conclusionsConventional therapies can be effective in gATM carriers and should be considered before PARPi, which shows limited efficacy in this group. Men with gATM mutations warrant prioritization for novel treatment strategies.

Indexed as

Prostatic Neoplasms, Castration-ResistantAndrostenesAntineoplastic AgentsAtaxia Telangiectasia Mutated ProteinsBenzamidesBRCA2 ProteinDocetaxelGerm-Line MutationHumansMaleMedication Therapy ManagementMiddle AgedNeoplasm GradingNeoplasm StagingNitrilesPatient SelectionabirateroneAndrostenesAntineoplastic AgentsAtaxia Telangiectasia Mutated ProteinsATM protein, humanBenzamidesBRCA2 ProteinBRCA2 protein, humanDocetaxelenzalutamideNitrilesPhenylthiohydantoinPoly(ADP-ribose) Polymerase InhibitorsProstate-Specific AntigenabirateroneATMBRCA2docetaxelenzalutamidegermlinehomologous recombination deficiencyPARPiplatinum

Identifiers

PMID34516663
PMCPMC8563438
OpenAlexW3200765540

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.