Evidence map›Paper›PMID 37190285›Full record

ReviewCancers2023

PARP Inhibitors in Breast and Ovarian Cancer.

Samuel S Y Wang, Yeo Ee Jie, Sim Wey Cheng, Goh Liuh Ling, Heong Valerie Yue Ming

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
11.3field-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

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  7. Article
  8. Review
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  10. Review
  11. Review
  12. Review
  13. International journal of oncology · 2025
    Review
  14. Article
  15. Development and evaluation of aEJNMMI radiopharmacy and chemistry · 2025
    Article
  16. Article
  17. Article
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  19. Article
  20. 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 1 institution in 1 country.

Samuel S Y WangMedical Oncology, Tan Tock Seng Hospital, Singapore 308433, Singapore.ORCID 0000-0002-1013-7364
Yeo Ee JieMedical Oncology, Tan Tock Seng Hospital, Singapore 308433, Singapore.
Sim Wey ChengMolecular Diagnostic Laboratory, Tan Tock Seng Hospital, Singapore 308433, Singapore.
Goh Liuh LingMolecular Diagnostic Laboratory, Tan Tock Seng Hospital, Singapore 308433, Singapore.
Heong Valerie Yue MingMedical Oncology, Tan Tock Seng Hospital, Singapore 308433, Singapore.ORCID 0000-0001-8894-1355
Tan Tock Seng Hospital · SG

Funding

CSCS-LKC-NHG CSCS 20001
6 · The paper itself

Abstract

Poly (ADP-ribose) polymerase (PARP) inhibitors are one of the most successful examples of clinical translation of targeted therapies in medical oncology, and this has been demonstrated by their effective management of BRCA1/BRCA2 mutant cancers, most notably in breast and ovarian cancers. PARP inhibitors target DNA repair pathways that BRCA1/2-mutant tumours are dependent upon. Inhibition of the key components of these pathways leads to DNA damage triggering subsequent critical levels of genomic instability, mitotic catastrophe and cell death. This ultimately results in a synthetic lethal relationship between BRCA1/2 and PARP, which underpins the effectiveness of PARP inhibitors. Despite the early and dramatic response seen with PARP inhibitors, patients receiving them often develop treatment resistance. To date, data from both clinical and preclinical studies have highlighted multiple resistance mechanisms to PARP inhibitors, and only by understanding these mechanisms are we able to overcome the challenges. The focus of this review is to summarise the underlying mechanisms underpinning treatment resistance to PARP inhibitors and to aid both clinicians and scientists to develop better clinically applicable assays to better select patients who would derive the greatest benefit as well as develop new novel/combination treatment strategies to overcome these mechanisms of resistance. With a better understanding of PARP inhibitor resistance mechanisms, we would not only be able to identify a subset of patients who are unlikely to benefit from therapy but also to sequence our treatment paradigm to avoid and overcome these resistance mechanisms.

Indexed as

BRACA2BRCA1breast cancerovarian cancerPARP inhibitor

Identifiers

PMID37190285
PMCPMC10137187
OpenAlexW4366425126

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.