Evidence map›Paper›PMID 38236558›Full record

ReviewCurrent oncology reports2024

PARP Inhibitors in Breast Cancer: a Short Communication.

Gordon R Daly, Maen Monketh AlRawashdeh, Jason McGrath, Gavin P Dowling, Luke Cox, Sindhuja Naidoo, Damir Vareslija, Arnold D K Hill, Leonie Young

Open access · hybridAbstract readReview
In one paragraph

Review in Current oncology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
7.1field-weighted citation impact, top 2% 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, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Development and evaluation of aEJNMMI radiopharmacy and chemistry · 2025
    Article
  12. Review
  13. Somatic and germline aberrations in homologous recombination repair genes among Chinese high-risk breast cancer patients by multi-gene next-generation sequencing.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. 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

9 authors at 1 institution in 1 country.

Gordon R Daly *The Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland. gordondaly@rcsi.com.ORCID 0000-0001-8976-0839
Maen Monketh AlRawashdeh *The Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.
Jason McGrath *The Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.
Gavin P DowlingThe Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.
Luke CoxThe Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.
Sindhuja NaidooThe Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.
Damir VareslijaThe Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.
Arnold D K HillThe Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.
Leonie YoungThe Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.
Royal College of Surgeons in Ireland · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewIn the last decade, poly (ADP-ribose) polymerase (PARP) inhibitors have been approved in the treatment of several cancers, such as breast and ovarian cancer. This article aims to discuss the current uses, limitations, and future directions for PARP inhibitors (PARPis) in the treatment of breast cancer. RECENT

findingsFollowing the results of the OlympiAD and EMBRACA trials, PARPis were approved in HER2-negative breast cancer with a germline BRCA mutation. We reviewed this class of drugs' mechanism of action, efficacy, and limitations, as well as further studies that discussed resistance, impaired homologous recombination repair (HRR), and the combination of PARPis with other drugs. Improving understanding of HRR, increasing the ability to target resistance, and combining PARPis with other novel agents are continuing to increase the clinical utility of PARPis.

Indexed as

Breast NeoplasmsOvarian NeoplasmsDNA RepairFemaleHumansPoly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) PolymerasesPoly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) PolymerasesBRCABreast cancerHomologous repair deficiencyPARP inhibitor

Identifiers

PMID38236558
PMCPMC10891270
OpenAlexW4390987130

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.