Evidence map›Paper›PMID 34285060›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

Improving Risk Stratification for Pediatric Patients with Rhabdomyosarcoma by Molecular Detection of Disseminated Disease.

Nathalie S M Lak, Timon L Voormanns, Lily Zappeij-Kannegieter, Lieke M J van Zogchel, Marta Fiocco, Max M van Noesel, Johannes H M Merks, C Ellen van der Schoot, Godelieve A M Tytgat, Janine Stutterheim

Open access · hybridAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. 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
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

10 authors at 3 institutions in 1 country.

Nathalie S M LakPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0003-3743-8826
Timon L VoormannsSanquin Research, Amsterdam, the Netherlands.
Lily Zappeij-KannegieterSanquin Research, Amsterdam, the Netherlands.
Lieke M J van ZogchelPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0003-3557-7195
Marta FioccoPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Max M van NoeselPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Johannes H M MerksPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
C Ellen van der SchootSanquin Research, Amsterdam, the Netherlands.
Godelieve A M Tytgat *Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Janine Stutterheim *Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands. j.stutterheim@prinsesmaximacentrum.nl.
Sanquin · NLPrincess Máxima Center · NLLeiden University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSurvival of children with rhabdomyosarcoma that suffer from recurrent or progressive disease is poor. Identifying these patients upfront remains challenging, indicating a need for improvement of risk stratification. Detection of tumor-derived mRNA in bone marrow (BM) and peripheral blood (PB) using reverse-transcriptase qPCR (RT-qPCR) is a more sensitive method to detect disseminated disease. We identified a panel of genes to optimize risk stratification by RT-qPCR. EXPERIMENTAL

designCandidate genes were selected using gene expression data from rhabdomyosarcoma and healthy hematologic tissues, and a multiplexed RT-qPCR was developed. Significance of molecular disease was determined in a cohort of 99 Dutch patients with rhabdomyosarcoma (72 localized and 27 metastasized) treated according to the European pediatric Soft tissue sarcoma Study Group (EpSSG) RMS2005 protocol.

resultsWe identified the following 11 rhabdomyosarcoma markers:

conclusionsThis study shows a strong association between PCR-based detection of disseminated disease at diagnosis with clinical outcome in pediatric patients with rhabdomyosarcoma, also compared with conventional risk stratification. This warrants further validation in prospective trials as additional technique for risk stratification.

Indexed as

ChildChild, PreschoolFemaleHumansInfantMaleProspective StudiesReverse Transcriptase Polymerase Chain ReactionRhabdomyosarcomaRisk Assessment

Identifiers

PMID34285060
PMCPMC9401561
OpenAlexW3183826160

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.