Evidence map›Paper›PMID 29572535›Full record

ArticleNature communications2018

Poly-ligand profiling differentiates trastuzumab-treated breast cancer patients according to their outcomes.

Valeriy Domenyuk, Zoran Gatalica, Radhika Santhanam, Xixi Wei, Adam Stark, Patrick Kennedy, Brandon Toussaint, Symon Levenberg, Jie Wang, Nianqing Xiao and 19 more

Abstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
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  15. Article
  16. HER2 Directed Antibody-Drug-Conjugates beyond T-DM1 in Breast Cancer.International journal of molecular sciences · 2019
    Review
  17. Recent Progress in European Advanced Therapy Medicinal Products and Beyond.Frontiers in bioengineering and biotechnology · 2018
    Article
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

29 authors.

Valeriy DomenyukCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Zoran GatalicaCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Radhika SanthanamCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Xixi WeiCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Adam StarkCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Patrick KennedyCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Brandon ToussaintCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Symon LevenbergCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Jie WangCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Nianqing XiaoCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Richard GreilIIIrd Medical Department, Oncologic Center, Paracelsus Medical University Salzburg, Austria and Salzburg Cancer Research Institute, and Cancer Cluster Salzburg, Müllner Hauptstraße, 48A-5020, Salzburg, Austria.
Gabriel RinnerthalerIIIrd Medical Department, Oncologic Center, Paracelsus Medical University Salzburg, Austria and Salzburg Cancer Research Institute, and Cancer Cluster Salzburg, Müllner Hauptstraße, 48A-5020, Salzburg, Austria.
Simon P GampenriederIIIrd Medical Department, Oncologic Center, Paracelsus Medical University Salzburg, Austria and Salzburg Cancer Research Institute, and Cancer Cluster Salzburg, Müllner Hauptstraße, 48A-5020, Salzburg, Austria.
Amy B HeimbergerDepartment of Neurosurgery, University of Texas MD Anderson Cancer Center, 1400 Holcombe Boulevard, Houston, TX, 77030, USA.
Donald A BerryBerry Consultants, LLC, 3345 Bee Caves Road, Suite 201, Austin, TX, 78746, USA.
Anna BarkerComplex Adaptive Systems Initiative, Arizona State University, 1475N. Scottsdale Road, Suite 361, Scottsdale, AZ, 85257, USA.
John QuackenbushDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA, 02215-5450, USA.ORCID http://orcid.org/0000-0002-2702-5879
John L MarshallDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, 3800 Reservoir Road, N.W., Washington, DC, 20057, USA.
George PosteCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Jeffrey L VacircaNorth Shore Hematology Oncology Associates Cancer Center, 226N Belle Mead Road, East Setauket, NY, 11733, USA.
Gregory A VidalDivision of Hematology and Oncology, University of Tennessee Health Science Center, 7945 Wolf River Boulevard, Memphis, TN, 38138, USA.
Lee S SchwartzbergDivision of Hematology and Oncology, University of Tennessee Health Science Center, 7945 Wolf River Boulevard, Memphis, TN, 38138, USA.
David D HalbertCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Andreas VossCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Daniel MageeCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Mark R MiglareseCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA.
Michael FamulokCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA. m.famulok@uni-bonn.de.ORCID http://orcid.org/0000-0001-5878-6577
Günter MayerCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA. gmayer@uni-bonn.de.
David SpetzlerCaris Life Sciences, 4610 South 44th Place, Phoenix, AZ, 85040, USA. dspetzler@carisls.com.

Funding

Center for Clinical and Translational Sciences (CCTS)UL1TR000371 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2012 to 2016
$13.4M
Statistical Methods for Analysis of Massive Genetic and Genomic Data in Cancer ResearchR35CA197449 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI XIHONG LIN · 2015 to 2026
$10.9M
NCATS NIH HHS UL1 TR000371NCI NIH HHS R35 CA197449
6 · The paper itself

Abstract

Assessing the phenotypic diversity underlying tumour progression requires the identification of variations in the respective molecular interaction networks. Here we report proof-of-concept for a platform called poly-ligand profiling (PLP) that surveys these system states and distinguishes breast cancer patients who did or did not derive benefit from trastuzumab. We perform tissue-SELEX on breast cancer specimens to enrich single-stranded DNA (ssDNA) libraries that preferentially interact with molecular components associated with the two clinical phenotypes. Testing of independent sample sets verifies the ability of PLP to classify trastuzumab-treated patients according to their clinical outcomes with ROC-AUC of 0.78. Standard HER2 testing of the same patients gives a ROC-AUC of 0.47. Kaplan-Meier analysis reveals a median increase in benefit from trastuzumab-containing treatments of 300 days for PLP-positive compared to PLP-negative patients. If prospectively validated, PLP may increase success rates in precision oncology and clinical trials, thus improving both patient care and drug development.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsArea Under CurveBiomarkers, TumorBreast NeoplasmsDisease-Free SurvivalDisease ProgressionDNA, Single-StrandedFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateLigandsAntineoplastic Agents, ImmunologicalBiomarkers, TumorDNA, Single-StrandedLigandsTrastuzumab

Identifiers

PMID29572535
PMCPMC5865185

What OpenQuestion holds

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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.