Evidence map›Paper›PMID 32914026›Full record

ArticleJCO precision oncology2019

Predicting Expected Absolute Chemotherapy Treatment Benefit in Women With Early-Stage Breast Cancer Using EndoPredict, an Integrated 12-Gene Clinicomolecular Assay.

Hatem Soliman, Darl D Flake, Anthony Magliocco, Mark Robson, Lee Schwartzberg, Priyanka Sharma, Krystal Brown, Saskia Wehnelt, Ralf Kronenwett, Alexander Gutin and 3 more

Open access · greenAbstract read
In one paragraph

Article in JCO precision oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

13 authors at 8 institutions in 3 countries.

Hatem SolimanMoffitt Cancer Center, Tampa, FL.
Darl D FlakeMyriad Genetics, Salt Lake City, UT.
Anthony MaglioccoMoffitt Cancer Center, Tampa, FL.
Mark RobsonMemorial Sloan Kettering Cancer Center, New York, NY.
Lee SchwartzbergWest Cancer Center, Memphis, TN.
Priyanka SharmaUniversity of Kansas Medical Center, Kansas City, KS.
Krystal BrownMyriad Genetics, Salt Lake City, UT.
Saskia WehneltMyriad Genetics, Salt Lake City, UT.
Ralf KronenwettMyriad International, Cologne, Germany.
Alexander GutinMyriad Genetics, Salt Lake City, UT.
Johnathan LancasterMyriad Genetics, Salt Lake City, UT.
Jack CuzickQueen Mary University of London, London, United Kingdom.
William GradisharNorthwestern University, Chicago, IL.
Myriad Genetics · USMoffitt Cancer Center · USMemorial Sloan Kettering Cancer Center · USMyriad (Germany) · DENorthwestern University · USQueen Mary University of London · GBUniversity of Kansas Medical Center · USWest Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Cancer Research UK 16891Cancer Research UK 5032NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposePrevious studies have shown EndoPredict (EPclin), a test that integrates 12-gene expression data with nodal status and tumor size, to be predictive for risk of distant recurrence in women with estrogen receptor-positive, human epidermal growth factor receptor 2-negative early-stage breast cancer. Here, we modeled expected absolute chemotherapy benefit on the basis of EPclin test results.

methodsThe effect of chemotherapy was modeled using previously validated 10-year risk of distant recurrence as a function of EPclin score for patients treated without chemotherapy. Average relative chemotherapy benefit to reduce breast cancer distant recurrence was evaluated using a published meta-analysis from the Early Breast Cancer Trialists' Collaborative Group. Absolute chemotherapy benefit differences were estimated across a range of interaction strengths between relative chemotherapy benefit and EPclin score. The average absolute benefit was calculated for patients with high and low EPclin scores using the distribution of scores in 2,185 samples tested by Myriad Genetics.

resultsThe average expected absolute benefit of chemotherapy treatment for patients with a low EPclin score was 1.8% in the absence of interaction and 1.5% for maximal interaction. Conversely, the expected average absolute chemotherapy benefit for patients with a high EPclin score was 5.3% and 7.3% for no interaction and maximal interaction, respectively.

conclusionFor women with estrogen receptor-positive, human epidermal growth factor receptor 2-negative early-stage breast cancer, a high EPclin score identified which patients would benefit most from adjuvant chemotherapy in terms of absolute reduction of distant recurrence, regardless of the amount of interaction between EPclin and relative chemotherapy benefit. A high degree of prognostic discrimination for distant recurrence is more important for identifying patients likely to benefit most from chemotherapy than an interaction between EPclin and treatment-relative benefit.

Identifiers

PMID32914026
PMCPMC7446472
OpenAlexW2966629975

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.