Evidence map›Paper›PMID 35079231›Full record

ArticleContemporary oncology (Poznan, Poland)2021

Mutational landscape of primary and recurrent Ewing sarcoma.

Paulina Jagodzińska-Mucha, Paweł Sobczuk, Michał Mikuła, Anna Raciborska, Anna Dawidowska, Maria Kulecka, Katarzyna Bilska, Anna Szumera-Ciećkiewicz, Anna Kluska, Magdalena Piątkowska and 3 more

Open access · goldAbstract read
In one paragraph

Article in Contemporary oncology (Poznan, Poland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Review
  7. The Impact of PIK3R1 Mutations and Insulin-PI3K-Glycolytic Pathway Regulation in Prostate Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
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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

13 authors at 1 institution in 1 country.

Paulina Jagodzińska-MuchaDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Paweł SobczukDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Michał MikułaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Anna RaciborskaDepartment of Oncology and Surgical Oncology for Children and Youth, Mother and Child Institute, Warsaw, Poland.
Anna DawidowskaEarly Phase Clinical Trials Unit, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Maria KuleckaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Katarzyna BilskaDepartment of Oncology and Surgical Oncology for Children and Youth, Mother and Child Institute, Warsaw, Poland.
Anna Szumera-CiećkiewiczDepartment of Pathology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Anna KluskaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Magdalena PiątkowskaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Anna BałabasDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Piotr RutkowskiDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Iwona ŁugowskaDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
The Maria Sklodowska-Curie National Research Institute of Oncology · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionEwing sarcoma (ES) is a highly aggressive malignancy of bone and soft tissues characterized by the presence of a genetic fusion involving the AIM OF THE STUDY: The objective is to assess the mutational landscape of ES in pretreatment samples, tumor samples after neoadjuvant chemotherapy, and in metastatic/recurrent tumors in children and adults. MATERIAL AND

methodsDNA from 39 formalin-fixed paraffin-embedded tumor samples of 22 patients (17 adults, 5 children) were analyzed by targeted next generation sequencing (NGS) using the Oncomine Comprehensive Assay v3gene panel. Additional functional analyses were performed between patient subgroups.

resultsAll samples were characterized by low tumor mutation burden (< 10 mut/Mb). The most commonly mutated genes were

conclusionsBesides

Indexed as

Ewing sarcomageneticsmutationNGStargeted therapies

Identifiers

PMID35079231
PMCPMC8768047
OpenAlexW4205620992

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.