Evidence map›Paper›PMID 33799547›Full record

ArticleCancers2021

Potential Utility of Pre-Emptive Germline Pharmacogenetics in Breast Cancer.

Philip S Bernard, Whitney Wooderchak-Donahue, Mei Wei, Steven M Bray, Kevin C Wood, Baiju Parikh, Gwendolyn A McMillin

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

7 authors at 2 institutions in 1 country.

Philip S BernardARUP Institute for Clinical and Experimental Pathology, Salt Lake City, UT 84108, USA.
Whitney Wooderchak-DonahueARUP Institute for Clinical and Experimental Pathology, Salt Lake City, UT 84108, USA.
Mei WeiHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
Steven M BrayLifeOmic Inc., Indianapolis, IN 46202, USA.
Kevin C WoodLifeOmic Inc., Indianapolis, IN 46202, USA.
Baiju ParikhLifeOmic Inc., Indianapolis, IN 46202, USA.
Gwendolyn A McMillinARUP Institute for Clinical and Experimental Pathology, Salt Lake City, UT 84108, USA.
ARUP Laboratories (United States) · USHuntsman Cancer Institute · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
NCI NIH HHS P30 CA042014
6 · The paper itself

Abstract

Patients with breast cancer often receive many drugs to manage the cancer, side effects associated with cancer treatment, and co-morbidities (i.e., polypharmacy). Drug-drug and drug-gene interactions contribute to the risk of adverse events (AEs), which could lead to non-adherence and reduced efficacy. Here we investigated several well-characterized inherited (germline) pharmacogenetic (PGx) targets in 225 patients with breast cancer. All relevant clinical, pharmaceutical, and PGx diplotype data were aggregated into a single unifying informatics platform to enable an exploratory analysis of the cohort and to evaluate pharmacy ordering patterns. Of the drugs recorded, there were 38 for which high levels of evidence for clinical actionability with PGx was available from the US FDA and/or the Clinical Pharmacogenetics Implementation Consortium (CPIC). These data were associated with 10 pharmacogenes:

Indexed as

breast cancerCYP2D6genotypingpharmacogenomicssupportive care

Identifiers

PMID33799547
PMCPMC7998388
OpenAlexW3136419935

What Socratic 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 Socratic graph.