Evidence map›Paper›PMID 33287361›Full record

ArticleCancers2020

Detection of Structural Variants in Circulating Cell-Free DNA from Sarcoma Patients Using Next Generation Sequencing.

Lauren Mc Connell, Jana Gazdova, Katja Beck, Shambhavi Srivastava, Louise Harewood, J P Stewart, Daniel Hübschmann, Albrecht Stenzinger, Hanno Glimm, Christoph E Heilig and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 37% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Circulating Tumor DNA Is Prognostic in Intermediate-Risk Rhabdomyosarcoma: A Report From the Children's Oncology Group.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Molecular profiling of soft-tissue sarcomas with FoundationOneTherapeutic advances in medical oncology · 2021
    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

12 authors at 3 institutions in 2 countries.

Lauren Mc ConnellPatrick G Johnston Centre for Cancer Research, Queen's University, Belfast BT9 7AE, UK.ORCID 0000-0003-3396-698X
Jana GazdovaPatrick G Johnston Centre for Cancer Research, Queen's University, Belfast BT9 7AE, UK.
Katja BeckDepartment of Translational Medical Oncology, National Center for Tumor Diseases (NCT), 69120 Heidelberg, Germany.
Shambhavi SrivastavaPatrick G Johnston Centre for Cancer Research, Queen's University, Belfast BT9 7AE, UK.
Louise HarewoodPatrick G Johnston Centre for Cancer Research, Queen's University, Belfast BT9 7AE, UK.
J P StewartPatrick G Johnston Centre for Cancer Research, Queen's University, Belfast BT9 7AE, UK.
Daniel HübschmannComputational Oncology, Molecular Diagnostics Program, National Center for Tumor Diseases (NCT) Heidelberg and DKFZ, 69120 Heidelberg, Germany.ORCID 0000-0002-6041-7049
Albrecht StenzingerGerman Cancer Research Center, 69120 Heidelberg, Germany.
Hanno GlimmDepartment of Translational Medical Oncology, National Center for Tumor Diseases (NCT) Dresden and German Cancer Research Center (DKFZ), 01307 Dresden, Germany.
Christoph E HeiligDepartment of Translational Medical Oncology, National Center for Tumor Diseases (NCT), 69120 Heidelberg, Germany.ORCID 0000-0001-8869-1421
Stefan FröhlingDepartment of Translational Medical Oncology, National Center for Tumor Diseases (NCT), 69120 Heidelberg, Germany.ORCID 0000-0001-7907-4595
David GonzalezPatrick G Johnston Centre for Cancer Research, Queen's University, Belfast BT9 7AE, UK.ORCID 0000-0003-0580-5636
Queen's University Belfast · GBGerman Cancer Research Center · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating tumour DNA (ctDNA) analysis using next generation sequencing (NGS) is being implemented in clinical practice for treatment stratification and disease monitoring. However, using ctDNA to detect structural variants, a common occurrence in sarcoma, can be challenging. Here, we use a sarcoma-specific targeted NGS panel to identify translocations and copy number variants in a cohort of 12 tissue specimens and matched circulating cell-free DNA (cfDNA) from soft tissue sarcoma patients, including alveolar rhabdomyosarcoma (

Indexed as

cell-free DNAnext generation sequencingsarcomatranslocations

Identifiers

PMID33287361
PMCPMC7761870
OpenAlexW3109467684

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.