Evidence map›Paper›PMID 33015522›Full record

ArticleJCO precision oncology2019

Identification of Actionable Fusions as an Anti-EGFR Resistance Mechanism Using a Circulating Tumor DNA Assay.

Katherine Clifton, Thereasa A Rich, Christine Parseghian, Victoria M Raymond, Arvind Dasari, Allan Andresson Lima Pereira, Jason Willis, Jonathan M Loree, Todd M Bauer, Young Kwang Chae and 12 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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Circulating Tumor DNA Enables Sensitive Detection of Actionable Gene Fusions and Rearrangements Across Cancer Types.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  7. Circulating Tumor DNA to Drive Treatment in Metastatic Colorectal Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. The Pan-Tumor Landscape of Targetable Kinase Fusions in Circulating Tumor DNA.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  13. Article
  14. Review
  15. Review
  16. Liquid Biopsy, ctDNA Diagnosis through NGS.Life (Basel, Switzerland) · 2021
    Review
  17. Review
  18. Molecular Characterization and Therapeutic Targeting of Colorectal Cancers Harboring Receptor Tyrosine Kinase Fusions.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  19. 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

22 authors at 13 institutions in 1 country.

Katherine CliftonThe University of Texas MD Anderson Cancer Center, Houston, TX.
Thereasa A RichGuardantHealth, Redwood City, CA.
Christine ParseghianThe University of Texas MD Anderson Cancer Center, Houston, TX.
Victoria M RaymondGuardantHealth, Redwood City, CA.
Arvind DasariThe University of Texas MD Anderson Cancer Center, Houston, TX.
Allan Andresson Lima PereiraThe University of Texas MD Anderson Cancer Center, Houston, TX.
Jason WillisThe University of Texas MD Anderson Cancer Center, Houston, TX.
Jonathan M LoreeBC Cancer, Vancouver, British Columbia, Canada.
Todd M BauerTennessee Oncology Sarah Cannon Research Institute, Nashville, TN.
Young Kwang ChaeNorthwestern University Feinberg School of Medicine, Chicago, IL.
Gary SherrillCone Health Cancer Center, Greensboro, NC.
Paul FantaUniversity of San Diego Moores Cancer Center, La Jolla, CA.
Axel GrotheyThe University of Tennessee West Cancer Center, Memphis, TN.
Andrew HendifarCedars-Sinai Medical Center, Los Angeles, CA.
David HenryUniversity of Pennsylvania, Philadelphia, PA.
Daruka MahadevanThe University of Arizona Cancer Center, Tucson, AZ.
Mohammad Amin NezamiPacific Medical Center of Hope, Fresno, CA.
Benjamin TanWashington University School of Medicine, St Louis, MO.
Zev A WainbergUniversity of California Los Angeles, Los Angeles, CA.
Richard LanmanGuardantHealth, Redwood City, CA.
Scott KopetzThe University of Texas MD Anderson Cancer Center, Houston, TX.
Van MorrisThe University of Texas MD Anderson Cancer Center, Houston, TX.
The University of Texas MD Anderson Cancer Center · USGuardant (United States) · USCedars-Sinai Medical Center · USCone Health · USNorthwestern University · USPacific Tower · USSarah Cannon · USUniversity of Arizona · USUniversity of California, Los Angeles · USUniversity of Pennsylvania · USUniversity of San Diego · USUniversity of Tennessee at Knoxville · USWashington University in St. Louis · US

Funding

Paul Calabresi Clinical Oncology AwardK12CA088084 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI David S. Hong, Scott Kopetz · 2000 to 2026
$14.0M
TRAINING FOR ACADEMIC ONCOLOGY/HEMATOLOGYT32CA009666 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Michael Davies, Courtney DiNardo · 1994 to 2026
$9.8M
NCI NIH HHS K12 CA088084NCI NIH HHS T32 CA009666
6 · The paper itself

Abstract

purposeGene fusions are established oncogenic drivers and emerging therapeutic targets in advanced colorectal cancer. This study aimed to detail the frequencies and clinicopathological features of gene fusions in colorectal cancer using a circulating tumor DNA assay.

methodsCirculating tumor DNA samples in patients with advanced colorectal cancer were analyzed at 4,581 unique time points using a validated plasma-based multigene assay that includes assessment of fusions in

resultsForty-four unique fusions were identified in 40 (1.1%) of the 3,808 patients with circulating tumor DNA detected:

conclusionDiverse and potentially actionable fusions can be detected using a circulating tumor DNA assay in patients with advanced colorectal cancer. Distribution of coexisting subclonal mutations in

Identifiers

PMID33015522
PMCPMC7526699
OpenAlexW2977377261

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.