Evidence map›Paper›PMID 33266287›Full record

ArticleCancers2020

The Health-Related Quality of Life of Sarcoma Patients and Survivors in Germany-Cross-Sectional Results of a Nationwide Observational Study (PROSa).

Martin Eichler, Leopold Hentschel, Stephan Richter, Peter Hohenberger, Bernd Kasper, Dimosthenis Andreou, Daniel Pink, Jens Jakob, Susanne Singer, Robert Grützmann and 15 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 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
4.3field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 2 syntheses or guidelines pooled it, 56 citations in OpenAlex.

  1. Twenty-five years of experience with patient-reported outcome measures in soft-tissue sarcoma patients: a systematic review.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2024
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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

25 authors at 11 institutions in 1 country.

Martin EichlerClinic and Polyclinic for Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, 01307 Dresden, Germany.ORCID 0000-0001-9654-2207
Leopold HentschelNational Center for Tumor Diseases (NCT/UCC), 01307 Dresden, Germany.
Stephan RichterClinic and Polyclinic for Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, 01307 Dresden, Germany.
Peter HohenbergerDivision of Surgical Oncology & Thoracic Surgery, Mannheim University Medical Center, University of Heidelberg, 68167 Mannheim, Germany.
Bernd KasperInterdisciplinary Tumor Center, Sarcoma Unit, University Medical Center Mannheim, 68167 Mannheim, Germany.ORCID 0000-0001-8425-8356
Dimosthenis AndreouDepartment of General Orthopedics and Tumor Orthopedics, University Hospital Munster, 48149 Munster, Germany.ORCID 0000-0002-5083-9678
Daniel PinkSarcoma Center Berlin-Brandenburg, Helios Hospital Bad Saarow, 15526 Bad Saarow, Germany.ORCID 0000-0001-7243-7373
Jens JakobClinic for General, Visceral, and Pediatric Surgery, University Hospital Goettingen, 37075 Goettingen, Germany.
Susanne SingerInstitute for Medical Biostatistics, Epidemiology and Informatic, University Hospital Mainz, 55131 Mainz, Germany.ORCID 0000-0001-5784-7964
Robert GrützmannClinic for Surgery, University Hospital Erlangen, 91054 Erlangen, Germany.
Stephen FungClinic for General, Visceral, and Pediatric Surgery, University Hospital Dusseldorf, 40225 Dusseldorf, Germany.
Eva WardelmannGerhard-Domagk-Institute for Pathology, University Hospital Munster, 48149 Munster, Germany.
Karin ArndtGerman Sarcoma Foundation, 61200 Woelfersheim, Germany.
Vitali HeidtThe Scientific Institute of Office-based Hematologists and Oncologists, 50676 Cologne, Germany.
Christine HofbauerNational Center for Tumor Diseases (NCT/UCC), 01307 Dresden, Germany.
Marius FriedClinic and Polyclinic for Internal Medicine III/University-Centre for Tumor Diseases, University Hospital Mainz, 55131 Mainz, Germany.
Verena I GaidzikClinic for Internal Medicine III, University Hospital Ulm, 89081 Ulm, Germany.
Karl VerpoortInter-Local Joint Practice, Dres. Verpoort, Wierecky & Brandl, 20259 Hamburg, Germany.
Marit AhrensMedical Clinic II, University Hospital Frankfurt, 60590 Frankfurt am Main, Germany.
Jürgen WeitzNational Center for Tumor Diseases (NCT/UCC), 01307 Dresden, Germany.
Klaus-Dieter SchaserNational Center for Tumor Diseases (NCT/UCC), 01307 Dresden, Germany.
Martin BornhäuserClinic and Polyclinic for Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, 01307 Dresden, Germany.
Jochen SchmittNational Center for Tumor Diseases (NCT/UCC), 01307 Dresden, Germany.
Markus K SchulerClinic and Polyclinic for Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, 01307 Dresden, Germany.ORCID 0000-0003-0764-1049
The PROSa Study Group
National Center for Tumor Diseases · DEHeidelberg University · DEJohannes Gutenberg University Mainz · DEUniversity Hospital Münster · DEDüsseldorf University Hospital · DEGoethe University Frankfurt · DEHelios Klinikum Emil von Behring · DEUniversitätsklinikum Erlangen · DEUniversitätsmedizin Greifswald · DEUniversity Hospital Carl Gustav Carus · DEUniversity Hospital Ulm · DE

Funding

Deutsche Krebshilfe 111713
6 · The paper itself

Abstract

Sarcomas are rare cancers with high heterogeneity in terms of type, location, and treatment. The health-related quality of life (HRQoL) of sarcoma patients has rarely been investigated and is the subject of this analysis. Adult sarcoma patients and survivors were assessed between September 2017 and February 2019 in 39 study centers in Germany using standardized, validated questionnaires (European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30)). Associated factors were analyzed exploratively using multivariable linear regressions. Among 1113 patients, clinically important limitations and symptoms were most pronounced in emotional (63%, 95% CI 60-66%), physical (60%, 95% CI 57-62%), role functioning (51%, 95% CI 48-54%), and pain (56%, 95% CI 53-59%) and fatigue (51%, 95% CI 48-54%). HRQoL differed between tumor locations with lower extremities performing the worst and sarcoma types with bone sarcoma types being most affected. Additionally, female gender, higher age, lower socioeconomic status, recurrent disease, not being in retirement, comorbidities, and being in treatment were associated with lower HRQoL. Sarcoma patients are severely restricted in their HRQoL, especially in functioning scales. The heterogeneity of sarcomas with regard to type and location is reflected in HRQoL outcomes. During treatment and follow-up, close attention has to be paid to the reintegration of the patients into daily life as well as to their physical abilities and emotional distress.

Indexed as

clinically important restrictions and symptomshealth-related quality of lifeobservational studyrare diseasesarcoma

Identifiers

PMID33266287
PMCPMC7759994
OpenAlexW3110333748

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.