Evidence map›Paper›PMID 32220886›Full record

Observational studyClinical cancer research : an official journal of the American Association for Cancer Research2020

Whole-Exome Sequencing Analysis of the Progression from Non-Low-Grade Ductal Carcinoma

Fresia Pareja, David N Brown, Ju Youn Lee, Arnaud Da Cruz Paula, Pier Selenica, Rui Bi, Felipe C Geyer, Andrea Gazzo, Edaise M da Silva, Mahsa Vahdatinia and 6 more

Abstract readObservational Study
In one paragraph

Observational study in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Elucidating cooperative genetic events in DCIS progression in mutantProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Clinicopathologic Features, Molecular Landscape, and Prognostic Implications of Ovarian Low-grade Serous Tumors with Histologic Transformation.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  14. Article
  15. Review
  16. Article
  17. Molecular Basis of Breast Tumor Heterogeneity.Advances in experimental medicine and biology · 2025
    Review
  18. The Microenvironment in DCIS and Its Role in Disease Progression.Advances in experimental medicine and biology · 2025
    Review
  19. Article
  20. 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

16 authors.

Fresia Pareja *Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
David N Brown *Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Ju Youn Lee *Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Arnaud Da Cruz Paula *Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Pier SelenicaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Rui BiDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Felipe C GeyerDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Andrea GazzoDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Edaise M da SilvaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Mahsa VahdatiniaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-9424-537X
Anthe A StylianouDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Lorenzo FerrandoDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-4025-7930
Hannah Y WenDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
James B HicksDepartment of Biological Sciences, University of Southern California, Los Angeles, California.ORCID 0000-0001-5353-4338
Britta WeigeltDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York. reisfilj@mskcc.org weigeltb@mskcc.org.
Jorge S Reis-FilhoDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York. reisfilj@mskcc.org weigeltb@mskcc.org.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
MSK Paul Calabresi Career Development Award for Clinical OncologyK12CA184746 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Omar Abdel-Wahab, Simon N. Powell · 2015 to 2026
$8.3M
NCI NIH HHS K12 CA184746NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeDuctal carcinoma EXPERIMENTAL

designSynchronous DCIS (

resultsDCIS revealed genetic alterations similar to those of synchronously diagnosed IDC-NSTs and of non-related IDC-NSTs from The Cancer Genome Atlas (TCGA), whereas pure DCIS lacked

conclusionsIntralesion genetic heterogeneity is a common feature in DCIS synchronously diagnosed with IDC-NST. DCIS is a nonobligate precursor of IDC-NST, whose mechanisms of progression to invasive breast cancer are diverse and vary from case to case.

Indexed as

Genetic HeterogeneityAdultAgedBiomarkers, TumorBreastBreast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, Intraductal, NoninfiltratingClass I Phosphatidylinositol 3-KinasesDisease ProgressionDNA Copy Number VariationsDNA Mutational AnalysisExome SequencingFemaleHumansMiddle AgedBiomarkers, TumorClass I Phosphatidylinositol 3-KinasesPIK3CA protein, human

Identifiers

PMID32220886
PMCPMC7367727

What OpenQuestion holds

Textmetadata
LicenceTDM
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.