Evidence map›Paper›PMID 37119048›Full record

ArticleCancer medicine2023

Physical symptom burden in patients with desmoid-type fibromatosis and its impact on health-related quality of life and healthcare use.

Anne-Rose W Schut, Leanne E de Bruin, Belle H de Rooij, Emma Lidington, Milea J M Timbergen, Winette T A van der Graaf, Winan J van Houdt, Johannes J Bonenkamp, Robin L Jones, Dirk J Grünhagen and 4 more

Abstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Percutaneous Management of Desmoid Tumors.Current oncology reports · 2026
    Review
  2. Article
  3. Management of Desmoid Tumors.Current oncology reports · 2025
    Review
  4. Article
  5. Review
  6. 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

14 authors.

Anne-Rose W SchutDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0002-5131-6959
Leanne E de BruinDepartment of Surgical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Belle H de RooijDepartment of Research and Development, Netherlands Comprehensive Cancer Organisation, Utrecht, The Netherlands.ORCID 0000-0002-0172-0857
Emma LidingtonSarcoma Unit, Royal Marsden NHS Foundation Trust, London, UK.ORCID 0000-0001-6176-8054
Milea J M TimbergenDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Winette T A van der GraafDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0001-7549-3338
Winan J van HoudtDepartment of Surgical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0002-2303-3468
Johannes J BonenkampDepartment of Surgical Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.
Robin L JonesSarcoma Unit, Royal Marsden NHS Foundation Trust, London, UK.ORCID 0000-0003-4173-3844
Dirk J GrünhagenDepartment of Surgical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0001-8293-6002
Stefan SleijferDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Spyridon GennatasSarcoma Unit, Royal Marsden NHS Foundation Trust, London, UK.ORCID 0000-0002-5635-7696
Cornelis VerhoefDepartment of Surgical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0001-9980-8613
Olga HussonDepartment of Surgical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0002-1387-8686

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDesmoid-type fibromatosis (DTF) has a highly variable clinical course with varying intensity of symptoms. The objectives of this study were to identify subgroups of DTF patients based on physical symptom burden and to compare symptom burden subgroups on health-related quality of life (HRQoL) and healthcare use (univariate and multivariate).

methodsDesmoid-type fibromatosis patients from the United Kingdom and the Netherlands received cross-sectional questionnaires on HRQoL (EORTC QLQ-C30), DTF-specific HRQoL (DTF-QoL) and healthcare utilisation. Latent class cluster analysis was performed to identify subgroups based on patients' symptom burden using EORTC QLQ-C30 and DTF-QoL physical symptom items. Multivariate linear and logistic regression analyses were conducted to examine associations of symptom burden with HRQoL and healthcare utilisation, respectively.

resultsAmong 235 DTF patients, four symptom burden clusters were identified, with low symptom burden (24%), intermediate symptom burden-low pain (20%), intermediate symptom burden-high pain (25%) and high symptom burden (31%). DTF patients with high symptom burden had clinically relevant lower HRQoL scores compared to patients with low and intermediate symptom burden (p < 0.001) and reported more general and DTF-related visits to their general practitioner compared to the low symptom burden cluster (p < 0.01). In the multivariate analyses, symptom burden was independently associated with both HRQoL and healthcare utilisation.

conclusionsThis study identified four distinct subgroups of DTF patients based on their level of symptom burden, with a considerable number of patients being highly symptomatic. Knowledge of the level of symptom burden DTF patients experience can help to identify patients at risk of poorer outcomes and tailor supportive care to the individual needs of DTF patients.

Indexed as

Desmoid TumorsQuality of LifeCross-Sectional StudiesDelivery of Health CareHumansPainSurveys and Questionnairesdesmoid tumourhealthcare utilisationhealth-related quality of lifepatient-reported outcomesrare diseases

Identifiers

PMID37119048
PMCPMC10315709

What OpenQuestion holds

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LicenceCC BY
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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.