Evidence map›Paper›PMID 38738581›Full record

SynthesisJournal of cachexia, sarcopenia and muscle2024

Body weight and composition endpoints in cancer cachexia clinical trials: Systematic Review 4 of the cachexia endpoints series.

Leo R Brown, Mariana S Sousa, Michael S Yule, Vickie E Baracos, Donald C McMillan, Jann Arends, Trude R Balstad, Asta Bye, Olav Dajani, Ross D Dolan and 15 more

Abstract readSystematic Review
In one paragraph

Synthesis in Journal of cachexia, sarcopenia and muscle, 2024. 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
–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

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

  1. Pooled it
  2. Pooled it
  3. Exercise as supportive care in advanced cancer-related weight loss: a feasibility study comparing patients with and without severe weight loss.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Trial
  4. Article
  5. Article
  6. Review
  7. Review
  8. Observational
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Role of Peptides in Skeletal Muscle Wasting: A Scoping Review.Journal of cachexia, sarcopenia and muscle · 2025
    Article
  18. Article
  19. Article
  20. 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

25 authors.

Leo R BrownClinical Surgery, The University of Edinburgh, Royal Infirmary of Edinburgh, Edinburgh, UK.ORCID https://orcid.org/0000-0001-6181-7020
Mariana S SousaImproving Palliative, Aged and Chronic Care Through Clinical Research and Translation (IMPACCT), University of Technology Sydney, Sydney, Australia.
Michael S YuleClinical Surgery, The University of Edinburgh, Royal Infirmary of Edinburgh, Edinburgh, UK.
Vickie E BaracosDepartment of Oncology, University of Alberta, Edmonton, Alberta, Canada.
Donald C McMillanAcademic Unit of Surgery, University of Glasgow, Glasgow Royal Infirmary, Glasgow, UK.
Jann ArendsDepartment of Medicine I, Medical Centre-University of Freiburg Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Trude R BalstadDepartment of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
Asta ByeDepartment of Oncology, Oslo University Hospital, Oslo, Norway.
Olav DajaniDepartment of Oncology, Oslo University Hospital, Oslo, Norway.
Ross D DolanAcademic Unit of Surgery, University of Glasgow, Glasgow Royal Infirmary, Glasgow, UK.
Marie T FallonInstitute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Edinburgh, UK.
Christine GreilDepartment of Medicine I, Medical Centre-University of Freiburg Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Marianne J HjermstadDepartment of Oncology, Oslo University Hospital, Oslo, Norway.
Gunnhild JakobsenDepartment of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
Matthew MaddocksCicely Saunders Institute of Palliative Care, Policy and Rehabilitation, King's College London, London, UK.
James McDonaldInstitute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Edinburgh, UK.
Inger O OttestadDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Iain PhillipsEdinburgh Cancer Centre, Western General Hospital, Edinburgh, UK.
Judith SayersClinical Surgery, The University of Edinburgh, Royal Infirmary of Edinburgh, Edinburgh, UK.
Melanie R SimpsonDepartment of Nursing and Health Promotion, Faculty of Health Sciences, Oslo Metropolitan University, Oslo, Norway.
Ola M VagnildhaugDepartment of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
Tora S SolheimDepartment of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
Barry J A LairdInstitute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Edinburgh, UK.
Richard J E SkipworthClinical Surgery, The University of Edinburgh, Royal Infirmary of Edinburgh, Edinburgh, UK.
Cancer Cachexia Endpoints Working Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significant variation exists in the outcomes used in cancer cachexia trials, including measures of body composition, which are often selected as primary or secondary endpoints. To date, there has been no review of the most commonly selected measures or their potential sensitivity to detect changes resulting from the interventions being examined. The aim of this systematic review is to assess the frequency and diversity of body composition measures that have been used in cancer cachexia trials. MEDLINE, Embase and Cochrane Library databases were systematically searched between January 1990 and June 2021. Eligible trials examined adults (≥18 years) who had received an intervention aiming to treat or attenuate the effects of cancer cachexia for >14 days. Trials were also of a prospective controlled design and included body weight or at least one anthropometric, bioelectrical or radiological endpoint pertaining to body composition, irrespective of the modality of intervention (e.g., pharmacological, nutritional, physical exercise and behavioural) or comparator. Trials with a sample size of <40 patients were excluded. Data extraction used Covidence software, and reporting followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidance. This review was prospectively registered (PROSPERO: CRD42022276710). A total of 84 clinical trials, comprising 13 016 patients, were eligible for inclusion. Non-small-cell lung cancer and pancreatic cancer were studied most frequently. The majority of trial interventions were pharmacological (52%) or nutritional (34%) in nature. The most frequently reported endpoints were assessments of body weight (68 trials, n = 11 561) followed by bioimpedance analysis (BIA)-based estimates (23 trials, n = 3140). Sixteen trials (n = 3052) included dual-energy X-ray absorptiometry (DEXA)-based endpoints, and computed tomography (CT) body composition was included in eight trials (n = 841). Discrepancies were evident when comparing the efficacy of interventions using BIA-based estimates of lean tissue mass against radiological assessment modalities. Body weight, BIA and DEXA-based endpoints have been most frequently used in cancer cachexia trials. Although the optimal endpoints cannot be determined from this review, body weight, alongside measurements from radiological body composition analysis, would seem appropriate. The choice of radiological modality is likely to be dependent on the trial setting, population and intervention in question. CT and magnetic resonance imaging, which have the ability to accurately discriminate tissue types, are likely to be more sensitive and provide greater detail. Endpoints are of particular importance when aligned with the intervention's mechanism of action and/or intended patient benefit.

Indexed as

Body CompositionBody WeightCachexiaNeoplasmsClinical Trials as TopicHumansbody compositioncachexiacancer cachexiaclinical trials

Identifiers

PMID38738581
PMCPMC11154800

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.