Evidence map›Paper›PMID 34916829›Full record

ReviewPharmacogenomics and personalized medicine2021

Ethnic Diversity of DPD Activity and the

Cassandra White, Rodney J Scott, Christine Paul, Andrew Ziolkowski, David Mossman, Stephen Ackland

Abstract readReview
In one paragraph

Review in Pharmacogenomics and personalized medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 3 pooled it
–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

20 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Observational
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  15. Overcoming Barriers to Discovery and Implementation of Equitable Pharmacogenomic Testing in Oncology.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Review
  16. Article
  17. Article
  18. Article
  19. Pharmacogenomics in the era of personalised medicine.The Medical journal of Australia · 2022
    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

6 authors.

Cassandra WhiteUniversity of Newcastle, Newcastle, NSW, Australia.ORCID 0000-0001-5268-2793
Rodney J ScottUniversity of Newcastle, Newcastle, NSW, Australia.
Christine PaulUniversity of Newcastle, Newcastle, NSW, Australia.
Andrew ZiolkowskiDivision of Molecular Medicine, Pathology North John Hunter Hospital, Newcastle, NSW, Australia.
David MossmanDivision of Molecular Medicine, Pathology North John Hunter Hospital, Newcastle, NSW, Australia.
Stephen AcklandUniversity of Newcastle, Newcastle, NSW, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pharmacogenomic screening can identify patients with gene variants that predispose them to the development of severe toxicity from fluoropyrimidine (FP) chemotherapy. Deficiency of the critical metabolic enzyme dihydropyrimidine dehydrogenase (DPD) leads to excessive toxicity on exposure to fluoropyrimidine chemotherapy. This can result in hospitalisation, intensive care admissions and even death. Upfront screening of the gene that encodes for DPD (

Indexed as

dihydropyrimidine dehydrogenaseDPYD genenon-Caucasianpharmacogenomics

Identifiers

PMID34916829
PMCPMC8668257

What OpenQuestion holds

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LicenceCC BY-NC
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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.