Evidence map›Paper›PMID 38140900›Full record

ArticleClinical trials (London, England)2024

Recommendations for assessing appearance concerns related to plexiform and cutaneous neurofibromas in neurofibromatosis 1 clinical trials.

Vanessa L Merker, Heather L Thompson, Pamela L Wolters, Frank D Buono, Cynthia M Hingtgen, Tena Rosser, Belinda Barton, Carolina Barnett, Taylor Smith, Diana Haberkamp and 5 more

Open access · greenAbstract read
In one paragraph

Article in Clinical trials (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

15 authors at 12 institutions in 3 countries.

Vanessa L MerkerDepartment of Neurology and Cancer Center, Massachusetts General Hospital, Boston, MA, USA.ORCID 0000-0002-4542-5227
Heather L ThompsonDepartment of Communication Sciences and Disorders, California State University, Sacramento, Sacramento, CA, USA.ORCID 0000-0002-4205-239X
Pamela L WoltersPediatric Oncology Branch, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0001-9319-6281
Frank D BuonoDepartment of Psychiatry, Yale School of Medicine, New Haven, CT, USA.
Cynthia M HingtgenNeurological Health, Corewell Health, Grand Rapids, MI, USA.
Tena RosserDivision of Neurology, Children's Hospital Los Angeles, Los Angeles, CA, USA.
Belinda BartonFaculty of Health, Discipline of Psychology, Southern Cross University, Coffs Harbour, NSW, Australia.ORCID 0000-0002-3157-2031
Carolina BarnettDivision of Neurology, Department of Medicine, University Health Network and University of Toronto, Toronto, ON, Canada.
Taylor SmithDepartment of Psychology and Child Development, California Polytechnic State University, San Luis Obispo, CA, USA.
Diana HaberkampNeurofibromatosis Midwest, Chicago, IL, USA.
Miranda L McManusDepartment of Biology, College of Charleston, Charleston, SC, USA.ORCID 0009-0001-5390-0518
Andrea BaldwinClinical Research Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
Irene P MossChildren's Tumor Foundation, New York, NY, USA.
Claas RöhlNF Kinder, NF Patients United, Vienna, Austria.
Staci MartinPediatric Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
National Cancer Institute · USCalifornia Polytechnic State University · USCalifornia State University, Sacramento · USChildren's Hospital of Los Angeles · USChildren's Tumor Foundation · USCollege of Charleston · USCorewell HealthFrederick National Laboratory for Cancer Research · USMassachusetts General Hospital · USSouthern Cross University · AUUniversity Health Network · CAYale University · US

Funding

Therapy for NF1-Related Tumors and other Genetic Tumor Predisposition SyndromesZIABC010801 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WIDEMANN, BRIGITTE · 2009 to 2020
$13.8M
Intramural NIH HHS ZIA BC010801
6 · The paper itself

Abstract

BACKGROUND/

aimsIndividuals with neurofibromatosis 1 may experience changes in their appearance due to physical manifestations of the disorders and/or treatment sequelae. Appearance concerns related to these physical changes can lead to psychological distress and poorer quality of life. While many neurofibromatosis 1 clinical trials focus on assessing changes in tumor volume, evaluating patients' perspectives on corresponding changes in symptoms such as physical appearance can be key secondary outcomes. We aimed to determine whether any existing patient-reported outcome measures are appropriate for evaluating changes in appearance concerns within neurofibromatosis 1 clinical trials.

methodsAfter updating our previously published systematic review process, we used it to identify and rate existing patient-reported outcome measures related to disfigurement and appearance. Using a systematic literature search and initial triage process, we focused on identifying patient-reported outcome measures that could be used to evaluate changes in appearance concerns in plexiform or cutaneous neurofibroma clinical trials in neurofibromatosis 1. Our revised Patient-Reported Outcome Rating and Acceptance Tool for Endpoints then was used to evaluate each published patient-reported outcome measures in five domains, including (1) respondent characteristics, (2) content validity, (3) scoring format and interpretability, (4) psychometric data, and (5) feasibility. The highest-rated patient-reported outcome measures were then re-reviewed in a side-by-side comparison to generate a final consensus recommendation.

resultsEleven measures assessing appearance concerns were reviewed and rated; no measures were explicitly designed to assess appearance concerns related to neurofibromatosis 1. The FACE-Q Craniofacial Module-Appearance Distress scale was the top-rated measure for potential use in neurofibromatosis 1 clinical trials. Strengths of the measure included that it was rigorously developed, included individuals with neurofibromatosis 1 in the validation sample, was applicable to children and adults, covered item topics deemed important by neurofibromatosis 1 patient representatives, exhibited good psychometric properties, and was feasible for use in neurofibromatosis 1 trials. Limitations included a lack of validation in older adults, no published information regarding sensitivity to change in clinical trials, and limited availability in languages other than English.

conclusionThe Response Evaluation in Neurofibromatosis and Schwannomatosis patient-reported outcome working group currently recommends the FACE-Q Craniofacial Module Appearance Distress scale to evaluate patient-reported changes in appearance concerns in clinical trials for neurofibromatosis 1-related plexiform or cutaneous neurofibromas. Additional research is needed to validate this measure in people with neurofibromatosis 1, including older adults and those with tumors in various body locations, and explore the effects of nontumor manifestations on appearance concerns in people with neurofibromatosis 1 and schwannomatosis.

Indexed as

NeurilemmomaNeurofibroma, PlexiformNeurofibromatosesNeurofibromatosis 1Skin NeoplasmsAgedChildHumansQuality of Lifeappearance concernsclinical trialscutaneous neurofibromadisfigurementNeurofibromatosis 1patient-centered outcomes researchpatient-reported outcomesphysical appearanceplexiform neurofibroma

Identifiers

PMID38140900
PMCPMC10922038
OpenAlexW4390145168

What OpenQuestion holds

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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.