Evidence map›Paper›PMID 33917592›Full record

ReviewBiomedicines2021

Changing the History of Prostate Cancer with New Targeted Therapies.

Susana Hernando Polo, Diana Moreno Muñoz, Adriana Carolina Rosero Rodríguez, Jorge Silva Ruiz, Diana Isabel Rosero Rodríguez, Felipe Couñago

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  3. Article
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  6. Article
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  8. Review
  9. AR and PI3K/AKT in Prostate Cancer: A Tale of Two Interconnected Pathways.International journal of molecular sciences · 2023
    Review
  10. Review
  11. Review
  12. Emerging Biomarker-Guided Therapies in Prostate Cancer.Current oncology (Toronto, Ont.) · 2022
    Review
  13. Review
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  15. Review
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

6 authors at 5 institutions in 1 country.

Susana Hernando PoloDepartment of Medical Oncology, Hospital Universitario Fundación Alcorcón, 28922 Madrid, Spain.
Diana Moreno MuñozDepartment of Medical Oncology, Hospital Universitario Fundación Alcorcón, 28922 Madrid, Spain.ORCID 0000-0002-1540-3393
Adriana Carolina Rosero RodríguezDepartment of Medical Oncology, Hospital Universitario del Henares, 28822 Madrid, Spain.ORCID 0000-0002-5144-0757
Jorge Silva RuizCentro Nacional de Investigaciones Oncológicas (CNIO), Unidad de Cáncer de Mama, 28029 Madrid, Spain.ORCID 0000-0001-7977-7039
Diana Isabel Rosero RodríguezDepartment of Medical Oncology, Hospital Universitario Ramón y Cajal, 28034 Madrid, Spain.
Felipe CouñagoDepartment of Radiation Oncology, Hospital Universitario Quirónsalud, 28223 Madrid, Spain.ORCID 0000-0001-7233-0234
Hospital Universitario Fundación Alcorcón · ESHospital La Luz · ESHospital Universitario del Henares · ESHospital Universitario Ramón y Cajal · ESSpanish National Cancer Research Centre · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The therapeutic landscape of metastatic castration-resistant prostate cancer (mCRPC) is changing due to the emergence of new targeted therapies for the treatment of different molecular subtypes. Some biomarkers are described as potential molecular targets different from classic androgen receptors (AR). Approximately 20-25% of mCRPCs have somatic or germline alterations in DNA repair genes involved in homologous recombination. These subtypes are usually associated with more aggressive disease. Inhibitors of the enzyme poly ADP ribose polymerase (PARPi) have demonstrated an important benefit in the treatment of these subtypes of tumors. However, tumors that resistant to PARPi and wildtype BRCA tumors do not benefit from these therapies. Recent studies are exploring drug combinations with phosphatidylinositol-3-kinase (PI3K) or protein kinase B (AKT) inhibitors, as mechanisms to overcome resistance or to induce BRCAness and synthetic lethality. This article reviews various different novel strategies to improve outcomes in patients with prostate cancer.

Indexed as

hormonal therapyimmunotherapyPARP inhibitorsprostate cancerPSMAtargeted therapy

Identifiers

PMID33917592
PMCPMC8067446
OpenAlexW3150352730

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.