Evidence map›Paper›PMID 36564459›Full record

ArticleProstate cancer and prostatic diseases2023

Bipolar androgen therapy plus olaparib in men with metastatic castration-resistant prostate cancer.

Michael T Schweizer, Roman Gulati, Todd Yezefski, Heather H Cheng, Elahe Mostaghel, Michael C Haffner, Radhika A Patel, Navonil De Sarkar, Gavin Ha, Ruth Dumpit and 12 more

Open access · greenAbstract read
In one paragraph

Article in Prostate cancer and prostatic diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 10% 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, 2 syntheses or guidelines pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  6. Lack of synergy between AR-targeted therapies and PARP inhibitors in homologous recombination-proficient prostate cancer.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  13. Estrogen Therapy Induces Receptor-Dependent DNA Damage Enhanced by PARP Inhibition in ER+ Breast Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
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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

22 authors at 3 institutions in 2 countries.

Michael T SchweizerDepartment of Medicine, University of Washington, Seattle, WA, USA. schweize@uw.edu.ORCID http://orcid.org/0000-0002-5510-0661
Roman GulatiPublic Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-7592-6567
Todd YezefskiDepartment of Medicine, University of Washington, Seattle, WA, USA.
Heather H ChengDepartment of Medicine, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-1365-0702
Elahe MostaghelDepartment of Medicine, University of Washington, Seattle, WA, USA.
Michael C HaffnerClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Radhika A PatelHuman Biology Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Navonil De SarkarHuman Biology Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Gavin HaPublic Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Ruth DumpitHuman Biology Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Brianna WooClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Aaron LinClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Patrick PanlasiguiClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-1428-1742
Nerina McDonaldClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Michael LaiClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Katie NegaDepartment of Medicine, University of Washington, Seattle, WA, USA.
Jeannette HammondClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Petros GrivasDepartment of Medicine, University of Washington, Seattle, WA, USA.
Andrew HsiehDepartment of Medicine, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-0897-1050
Bruce MontgomeryDepartment of Medicine, University of Washington, Seattle, WA, USA.
Peter S NelsonDepartment of Medicine, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-5451-5726
Evan Y YuDepartment of Medicine, University of Washington, Seattle, WA, USA.
Fred Hutch Cancer Center · USUniversity of Washington · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZA

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
Steroid Metabolism in Castration-Resistant Prostate CancerP01CA163227 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI PETER S NELSON · 2013 to 2026
$25.0M
Statistical modeling to support population and translational cancer researchR50CA221836 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Roman Gulati · 2017 to 2026
$2.0M
Targeting Vulnerabilities Exposed by Cancer Treatment-Induced Lineage PlasticityR01CA266452 · NCI · FRED HUTCHINSON CANCER CENTER · PI PETER S NELSON · 2022 to 2026
$2.0M
NCI NIH HHS P01 CA163227NCI NIH HHS P30 CA015704NCI NIH HHS P50 CA097186NCI NIH HHS R01 CA266452NCI NIH HHS R50 CA221836
6 · The paper itself

Abstract

backgroundBipolar androgen therapy (BAT) results in rapid fluctuation of testosterone (T) between near-castrate and supraphysiological levels and has shown promise in metastatic castration-resistant prostate cancer (mCRPC). Its clinical effects may be mediated through induction of DNA damage, and preclinical studies suggest synergy with PARP inhibitors. PATIENTS AND

methodsThis was a single-center, Phase II trial testing olaparib plus BAT (T cypionate/enanthate 400 mg every 28 days) with ongoing androgen deprivation. Planned recruitment was 30 subjects (equal proportions with/without homologous recombination repair [HRR] gene mutations) with mCRPC post abiraterone and/or enzalutamide. The primary objective was to determine PSA

resultsThirty-six patients enrolled and 6 discontinued prior to response assessment. In the ITT cohort, PSA

conclusionsBAT plus olaparib is associated with high response rates and long PFS. Clinical benefit was observed regardless of HRR gene mutational status.

Indexed as

Prostatic Neoplasms, Castration-ResistantAndrogen AntagonistsAndrogensHumansMaleNitrilesPhthalazinesPiperazinesProstate-Specific AntigenTreatment OutcomeAndrogen AntagonistsAndrogensNitrilesolaparibPhthalazinesPiperazinesProstate-Specific Antigen

Identifiers

PMID36564459
PMCPMC10286318
OpenAlexW4312128723

What OpenQuestion holds

Textmetadata
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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.