Evidence map›Paper›PMID 33115529›Full record

ReviewJournal of hematology & oncology2020

Novel therapies are changing treatment paradigms in metastatic prostate cancer.

Eric Powers, Georgia Sofia Karachaliou, Chester Kao, Michael R Harrison, Christopher J Hoimes, Daniel J George, Andrew J Armstrong, Tian Zhang

Open access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 2 pooled it
11.0field-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

75 citing papers in PubMed, 2 syntheses or guidelines pooled it, 118 citations in OpenAlex.

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15 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

Eric PowersDepartment of Medicine, Duke University, Durham, NC, 27710, USA.
Georgia Sofia KarachaliouDivision of Medical Oncology, Department of Medicine, Duke University, DUMC 103861, Durham, NC, 27710, USA.
Chester KaoDepartment of Medicine, Duke University, Durham, NC, 27710, USA.
Michael R HarrisonDivision of Medical Oncology, Department of Medicine, Duke University, DUMC 103861, Durham, NC, 27710, USA.
Christopher J HoimesDivision of Medical Oncology, Department of Medicine, Duke University, DUMC 103861, Durham, NC, 27710, USA.
Daniel J GeorgeDivision of Medical Oncology, Department of Medicine, Duke University, DUMC 103861, Durham, NC, 27710, USA.
Andrew J ArmstrongDivision of Medical Oncology, Department of Medicine, Duke University, DUMC 103861, Durham, NC, 27710, USA.
Tian ZhangDivision of Medical Oncology, Department of Medicine, Duke University, DUMC 103861, Durham, NC, 27710, USA. tian.zhang2@duke.edu.ORCID 0000-0001-8914-3531
Prostate Cancer Foundation · USDuke University · US

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI JOHN N. NORTON · 1985 to 2026
$174.8M
NCI NIH HHS P30 CA014236
6 · The paper itself

Abstract

Metastatic castration-resistant prostate cancer (mCRPC) remains a terminal diagnosis with an aggressive disease course despite currently approved therapeutics. The recent successful development of poly ADP-ribose polymerase (PARP) inhibitors for patients with mCRPC and mutations in DNA damage repair genes has added to the treatment armamentarium and improved personalized treatments for prostate cancer. Other promising therapeutic agents currently in clinical development include the radiotherapeutic 177-lutetium-prostate-specific membrane antigen (PSMA)-617 targeting PSMA-expressing prostate cancer and combinations of immunotherapy with currently effective treatment options for prostate cancer. Herein, we have highlighted the progress in systemic treatments for mCRPC and the promising agents currently in ongoing clinical trials.

Indexed as

Androgen Receptor AntagonistsAnimalsAntineoplastic AgentsClinical Trials as TopicDipeptidesHeterocyclic Compounds, 1-RingHumansLutetiumMaleNeoplasm MetastasisPoly(ADP-ribose) Polymerase InhibitorsProstate-Specific AntigenProstatic Neoplasms, Castration-ResistantRadioisotopesAndrogen Receptor AntagonistsAntineoplastic AgentsDipeptidesHeterocyclic Compounds, 1-RingLutetiumLutetium-177Poly(ADP-ribose) Polymerase InhibitorsProstate-Specific AntigenPSMA-617RadioisotopesAndrogen receptor inhibitors (ARIs)Castration-resistant prostate cancerMetastatic prostate cancerPolyadenosine diphosphate [ADP]-ribose polymerase (PARP) inhibitorProstate-specific membrane antigen (PSMA)

Identifiers

PMID33115529
PMCPMC7594418
OpenAlexW3095574415

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.