Evidence map›Paper›PMID 35892198›Full record

ReviewOpen biology2022

Opinion: PARP inhibitors in cancer-what do we still need to know?

Andrew J Wicks, Dragomir B Krastev, Stephen J Pettitt, Andrew N J Tutt, Christopher J Lord

Abstract readReview
In one paragraph

Review in Open biology, 2022. 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
–field-weighted citation impact
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.

  1. Article
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  3. Review
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  11. Targeting BRCA and PALB2 in Pancreatic Cancer.Current treatment options in oncology · 2024
    Review
  12. Review
  13. Article
  14. Article
  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

5 authors.

Andrew J WicksThe CRUK Gene Function Laboratory, The Institute of Cancer Research, London SW3 6JB, UK.ORCID 0000-0002-9307-3262
Dragomir B KrastevThe CRUK Gene Function Laboratory, The Institute of Cancer Research, London SW3 6JB, UK.
Stephen J PettittThe CRUK Gene Function Laboratory, The Institute of Cancer Research, London SW3 6JB, UK.
Andrew N J TuttBreast Cancer Now Toby Robins Breast Cancer Research Centre, The Institute of Cancer Research, London SW3 6JB, UK.
Christopher J LordThe CRUK Gene Function Laboratory, The Institute of Cancer Research, London SW3 6JB, UK.

Funding

Cancer Research UK 24439Department of Health
6 · The paper itself

Abstract

PARP inhibitors (PARPi) have been demonstrated to exhibit profound anti-tumour activity in individuals whose cancers have a defect in the homologous recombination DNA repair pathway. Here, we describe the current consensus as to how PARPi work and how drug resistance to these agents emerges. We discuss the need to refine the current repertoire of clinical-grade companion biomarkers to be used with PARPi, so that patient stratification can be improved, the early emergence of drug resistance can be detected and dose-limiting toxicity can be predicted. We also highlight current thoughts about how PARPi resistance might be treated.

Indexed as

NeoplasmsPoly(ADP-ribose) Polymerase InhibitorsDrug Resistance, NeoplasmHumansPoly(ADP-ribose) Polymerase Inhibitorsbiomarkerscancerdrug resistancePARP inhibitorssynthetic lethality

Identifiers

PMID35892198
PMCPMC9326299

What OpenQuestion holds

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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.