Evidence map›Paper›PMID 37101345›Full record

ReviewExpert review of anticancer therapy2023

Emerging treatment options for prostate cancer.

Mohammad Atiq, Elias Chandran, Fatima Karzai, Ravi A Madan, Jeanny B Aragon-Ching

Open access · greenAbstract readReview
In one paragraph

Review in Expert review of anticancer therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
4.4field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Emerging Immunotherapy Approaches for Treating Prostate Cancer.International journal of molecular sciences · 2023
    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

5 authors at 2 institutions in 1 country.

Mohammad AtiqGenitourinary Malignancy Branch, National Cancer Institute, Bethesda, MD, USA.
Elias ChandranGenitourinary Malignancy Branch, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0002-0150-7765
Fatima KarzaiGenitourinary Malignancy Branch, National Cancer Institute, Bethesda, MD, USA.
Ravi A MadanGenitourinary Malignancy Branch, National Cancer Institute, Bethesda, MD, USA.
Jeanny B Aragon-ChingGU Medical Oncology, Inova Schar Cancer Institute, Fairfax, VA, USA.ORCID 0000-0002-6714-141X
National Cancer Institute · USUniversity of Virginia · US

Funding

Evaluation of Immune-based Combinations in Prostate CancerZIABC011897 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MADAN, RAVI · 2019 to 2025
$3.1M
Natural History of Biochemically Recurrent Prostate CancerZIABC012118 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MADAN, RAVI · 2022 to 2025
$1.4M
Intramural NIH HHS ZIA BC012118
6 · The paper itself

Abstract

introductionProstate cancer treatment has rapidly evolved in the past few years. Androgen deprivation therapy has been the backbone of treatment for locally advanced and metastatic prostate cancer, but incremental benefits in survival have been shown by adding androgen-receptor pathway inhibitors (ARPI) across various spectrums of disease state. In addition, docetaxel chemotherapy remains the first-line chemotherapy regimen available with survival benefits shown with triplet therapy in those who are chemotherapy eligible. However, disease progression remains inevitable and novel agents such as radioligand therapy with lutetium have shown improvement in survival. AREAS COVERED: This review discusses the pivotal trials that led to the U.S. FDA approval of agents utilized in metastatic prostate cancer and explores the use of novel agents including prostate-specific membrane antigen-targeting agents, radioligands, cell-based therapy, chimeric antigen receptor T-cell, BiTE, and antibody drug conjugates. EXPERT OPINION: Treatment landscape for metastatic castrate-resistant prostate cancer (mCRPC) has evolved beyond additional agents with ARPI and/or docetaxel, including other treatments with sipuleucel-T, radium, cabazitaxel, PARP inhibitors, and lutetium, which have specific indications and roles in sequencing. Novel therapies remain critically needed after progression from lutetium.

Indexed as

Androgen AntagonistsProstatic Neoplasms, Castration-ResistantAndrogensDocetaxelHumansLutetiumMaleAndrogen AntagonistsAndrogensDocetaxelLutetiumAnti-androgenimmunotherapymetastatic prostate cancerprostate cancerradioligands

Identifiers

PMID37101345
PMCPMC10718079
OpenAlexW4367174721

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.