Evidence map›Paper›PMID 28391775›Full record

Observational studyBMC medicine2017

Patterns of care and outcomes of patients with METAstatic soft tissue SARComa in a real-life setting: the METASARC observational study.

Marion Savina, Axel Le Cesne, Jean-Yves Blay, Isabelle Ray-Coquard, Olivier Mir, Maud Toulmonde, Sophie Cousin, Philippe Terrier, Dominique Ranchere-Vince, Pierre Meeus and 9 more

3 registry-linked trialsOpen access · goldAbstract readObservational Study
In one paragraph

Observational study in BMC medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 120 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed, 5 pooled it
12.9field-weighted citation impact, top 1% 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.

NCT03977818 completednot on this map

Patterns of Care and Outcomes of Patients With METAstatic Soft Tissue SARComa in a Real-life Setting: the METASARC Observational Study

TypeobservationalSponsorInstitut BergoniéRan1990 to 2017Enrolled2,165ConditionsSarcoma, Metastases, Chemotherapy
NCT03978039 recruitingnot on this map

The "BCB-sarcomes" Database: the Database of the French Sarcoma Group Dedicated to the Collection of Clinical and Biological Data for All Sarcomas

Typeobservational_patient_registrySponsorInstitut BergoniéRan2010 to 2035Enrolled150,000ConditionsSarcomaArmsChemotherapy, Immunotherapeutic Agent, target treatment, Surgery, Radiotherapy
NCT06114173 early_phase1unknown statusnot on this mapstarted 2022, after this paper: background citation

Efficacy and Safety Study of Cardunolizumab in Soft Tissue Sarcoma After Failure of at Least Anthracycline-based Chemotherapy: a Single-arm Clinical Trial

TypeinterventionalSponsorXiangya Hospital of Central South UniversityRan2022 to 2024Enrolled15ConditionsSarcoma, Soft TissueArmsCardunilizumab
3 · Its place in the literature

Who cites it

120 citing papers in PubMed, 5 syntheses or guidelines pooled it, 207 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Soft Tissue Sarcoma, Version 2.2022, NCCN Clinical Practice Guidelines in Oncology.Journal of the National Comprehensive Cancer Network : JNCCN · 2022
    Guideline
  4. Pooled it
  5. Pooled it
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  9. First-line Anlotinib plus Anthracyclines and Ifosfamide Followed by Anlotinib Maintenance in Advanced Soft-Tissue Sarcoma: A Phase II Single-Arm Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Trial
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  16. Review
  17. Article
  18. Observational
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60 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 4 institutions in 1 country.

Marion SavinaClinical and Epidemiological Research Unit, Institut Bergonié, Bordeaux, France.
Axel Le CesneDepartment of Medicine, Institut Gustave Roussy, Villejui, France.
Jean-Yves BlayDepartment of Medicine, Centre Leon Berard, Lyon, France.
Isabelle Ray-CoquardDepartment of Medicine, Centre Leon Berard, Lyon, France.
Olivier MirDepartment of Medicine, Institut Gustave Roussy, Villejui, France.
Maud ToulmondeDepartment of Medicine, Institut Bergonié, Bordeaux, France.
Sophie CousinDepartment of Medicine, Institut Bergonié, Bordeaux, France.
Philippe TerrierDepartment of Pathology, Institut Gustave Roussy, Villejuif, France.
Dominique Ranchere-VinceDepartment of Pathology, Centre Leon Berard, Lyon, France.
Pierre MeeusDepartment of Surgery, Centre Leon Berard, Lyon, France.
Eberhard StoeckleDepartment of Surgery, Institut Bergonié, Bordeaux, France.
Charles HonoréDepartment of Surgery, Institut Gustave Roussy, Villejuif, France.
Paul SargosDepartment of Radiotherapy, Institut Bergonié, Bordeaux, France.
Marie-Pierre SunyachDepartment of Radiotherapy, Centre Leon Berard, Lyon, France.
Cécile Le PéchouxDepartment of Radiotherapy, Institut Gustave Roussy, Villejuif, France.
Antoine GiraudClinical and Epidemiological Research Unit, Institut Bergonié, Bordeaux, France.
Carine BelleraClinical and Epidemiological Research Unit, Institut Bergonié, Bordeaux, France.
François Le LoarerDepartment of Pathology, Institut Bergonié, Bordeaux, France.
Antoine ItalianoDepartment of Medicine, Institut Bergonié, Bordeaux, France. a.italiano@bordeaux.unicancer.fr.
Institut Bergonié · FRCentre Léon Bérard · FRInstitut Gustave Roussy · FRBordeaux Population Health · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWell-designed observational studies of individuals with rare tumors are needed to improve patient care, clinical investigations, and the education of healthcare professionals.

methodsThe patterns of care, outcomes, and prognostic factors of a cohort of 2225 patients with metastatic soft tissue sarcomas who were diagnosed between 1990 and 2013 and documented in the prospectively maintained database of the French Sarcoma Group were analyzed.

resultsThe median number of systemic treatments was 3 (range, 1-6); 27% of the patients did not receive any systemic treatment and 1054 (49%) patients underwent locoregional treatment of the metastasis. Half of the patients who underwent chemotherapy (n = 810) received an off-label drug. Leiomyosarcoma was associated with a significantly better outcome than the other histological subtypes. With the exception of leiomyosarcomas, the benefit of a greater than third-line regimen was very limited, with a median time to next treatment (TNT) and overall survival (OS) ranging between 2.3 and 3.7 months and 5.4 and 8.5 months, respectively. The TNT was highly correlated with OS. Female sex, leiomyosarcoma histology, locoregional treatment of metastases, inclusion in a clinical trial, and treatment with first-line polychemotherapy were significantly associated with improved OS in the multivariate analysis.

conclusionsThe combination of doxorubicin with a second drug, such as ifosfamide, represents a valid option, particularly when tumor shrinkage is expected to provide clinical benefits. After failure of the second-line therapy, best supportive care should be considered, particularly in patients with non-leiomyosarcoma histology who are not eligible to participate in a clinical trial. Locoregional treatment of metastasis should always be included in the therapeutic strategy when feasible. TNT may represent a useful surrogate endpoint for OS in clinical studies.

Indexed as

Practice Patterns, Physicians'AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsDoxorubicinFemaleHumansLeiomyosarcomaMaleMiddle AgedNeoplasm MetastasisSarcomaSoft Tissue NeoplasmsSurvival AnalysisTreatment OutcomeDoxorubicinChemotherapyMetastasesOutcomePatterns of careSarcomaSurgery

Identifiers

PMID28391775
PMCPMC5385590
OpenAlexW2605016673

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.