Evidence map›Paper›PMID 25070544›Full record

ArticleAnnals of oncology : official journal of the European Society for Medical Oncology2014

Response to chemotherapy is not related to chromosome instability in synovial sarcoma.

C Chakiba, P Lagarde, D Pissaloux, A Neuville, C Brulard, G Pérot, J M Coindre, P Terrier, D Ranchere-Vince, A Ferrari and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Annals of oncology : official journal of the European Society for Medical Oncology, 2014. 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
3.4field-weighted citation impact, top 8% 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, 35 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

20 authors at 10 institutions in 5 countries.

C ChakibaDepartment of Medical Oncology, Institut Bergonié; Université Victor Segalen Bordeaux 2; Institut National de la Santé et de la Recherche Medicale (INSERM), U916-Institut Bergonié.
P LagardeUniversité Victor Segalen Bordeaux 2; Institut National de la Santé et de la Recherche Medicale (INSERM), U916-Institut Bergonié; Department of Pathology, Institut Bergonié, Bordeaux.
D PissalouxDepartment of Pathology, Centre Léon Bérard, Lyon.
A NeuvilleUniversité Victor Segalen Bordeaux 2; Institut National de la Santé et de la Recherche Medicale (INSERM), U916-Institut Bergonié; Department of Pathology, Institut Bergonié, Bordeaux.
C BrulardInstitut National de la Santé et de la Recherche Medicale (INSERM), U916-Institut Bergonié.
G PérotInstitut National de la Santé et de la Recherche Medicale (INSERM), U916-Institut Bergonié; Department of Pathology, Institut Bergonié, Bordeaux.
J M CoindreUniversité Victor Segalen Bordeaux 2; Institut National de la Santé et de la Recherche Medicale (INSERM), U916-Institut Bergonié; Department of Pathology, Institut Bergonié, Bordeaux.
P TerrierDepartment of Pathology, Institut Gustave Roussy, Villejuif, France.
D Ranchere-VinceDepartment of Pathology, Centre Léon Bérard, Lyon.
A FerrariDepartment of Medical Oncology.
P ColliniDepartment of Pathology, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
A J H SuurmeijerDepartment of Pathology, University of Groningen University Medical Center, Groningen, The Netherlands.
J Y BlayDepartment of Medical Oncology, Centre Léon Berard, Lyon.
S A TerrisseDepartment of Medical Oncology, Institut Gustave Roussy, Villejuif.
S Piperno-NeumannDepartment of Medical Oncology, Institut Curie, Paris.
G AverousDepartment of Pathology, Centre Hospitalier Universitaire Hautepierre, Strasbourg.
B BuiDepartment of Medical Oncology, Institut Bergonié; Institut National de la Santé et de la Recherche Medicale (INSERM), U916-Institut Bergonié.
D OrbachDepartment of Pediatric Oncoloy, Institut Curie, Paris, France.
A ItalianoDepartment of Medical Oncology, Institut Bergonié; Institut National de la Santé et de la Recherche Medicale (INSERM), U916-Institut Bergonié.
F ChibonInstitut National de la Santé et de la Recherche Medicale (INSERM), U916-Institut Bergonié; Department of Pathology, Institut Bergonié, Bordeaux. Electronic address: f.chibon@bordeaux.unicancer.fr.
Centre Léon Bérard · FRInstitut Bergonié · FRVictor (Japan) · JPInserm · FRInstitut Curie · FRInstitut Gustave Roussy · FRFondazione IRCCS Istituto Nazionale dei Tumori · ITGalen University · BZHôpital d'Hautepierre · FRUniversity of Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSynovial sarcoma (SS) is an aggressive soft-tissue tumor. Despite being considered as a chemosensitive disease, the real impact of perioperative chemotherapy on metastasis-free survival (MFS) is controversial. We have shown that metastatic relapse of SS is strongly associated with genomic complexity. There are no data regarding the potential correlation between genomic complexity and response to chemotherapy. PATIENTS AND

methodsThe study population included 65 SS patients diagnosed between 1991 and 2013 and with available tissue material. Genomic profiling was carried out by using array-CGH. Forty-five SS out of the 65 patients were treated with neoadjuvant anthracycline/ifosfamide-based chemotherapy. Radiological response was assessed according to RECIST criteria. Histological response was defined by the percentage of recognizable tumor cells on the surgical specimen.

resultsGenomic complexity was significantly associated with MFS. However, there was no statistically significant association between radiological or histological response and genomic complexity.

conclusionThe absence of significant association between response to chemotherapy and genomic complexity suggests that the prognostic value of chromosome instability in SS is independent of response to chemotherapy; mechanisms leading to metastatic relapse of SS are intrinsic to the biology of the tumor and current cytotoxic drugs are only poorly efficient to prevent it.

Indexed as

PrognosisAdolescentAdultAgedChildChild, PreschoolChromosomal InstabilityFemaleGenome, HumanHumansIfosfamideMaleMiddle AgedNeoadjuvant TherapyNeoplasm Recurrence, LocalSarcoma, SynovialIfosfamidechemotherapygenomic indexprognosissynovial sarcoma

Identifiers

PMID25070544
PMCPMC4207728
OpenAlexW2128609422

What OpenQuestion holds

Textmetadata
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.