Evidence map›Paper›PMID 42334715›Full record

ArticleJournal of patient-reported outcomes2026

Assessing content validity of the functional assessment of cancer therapy-cutaneous T-cell lymphoma (FACT-CTCL): a qualitative study.

Caroline Raymundo, Jenny Jung Sun Park, Mengyang Di, Cecilia Larocca, David Cella, Michi M Shinohara

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Article in Journal of patient-reported outcomes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Caroline RaymundoUniversity of Washington School of Medicine, Seattle, USA.
Jenny Jung Sun ParkUniversity of Washington School of Medicine, Seattle, USA. jenny199@uw.edu.ORCID https://orcid.org/0009-0006-4898-0994
Mengyang DiFred Hutchinson Cancer Center, Seattle, USA.
Cecilia LaroccaDepartment of Dermatology, Brigham and Women's Hospital, Boston, USA.
David CellaDepartment of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, USA.
Michi M ShinoharaDepartment of Dermatology, University of Washington, Seattle, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCutaneous T-cell lymphomas (CTCLs) are a heterogeneous group of non-Hodgkin lymphomas characterized by neoplastic T cells in the skin. Common subtypes of CTCL are mycosis fungoides (MF) and Sézary syndrome (SS). Patients with MF/SS can experience significant symptoms that affect health-related quality of life (HRQoL). Although the Functional Assessment of Cancer Therapy-Cutaneous T-Cell Lymphoma (FACT-CTCL) was developed as a disease-specific patient-reported outcome measure (PROM) for MF/SS, qualitative evaluation of its content validity in the target population has not been assessed. We therefore evaluated the content validity of the FACT-CTCL in patients with MF/SS and clinicians with expertise in MF/SS.

methodsSemi-structured cognitive interviews of patients with a diagnosis of MF or SS, as well as healthcare providers with expertise in treating MF/SS were conducted in alignment with the Consensus-based Standards for the Selection of Health Measurement Instruments (COSMIN). Patients evaluated the relevance, comprehensibility, and comprehensiveness of the FACT-CTCL. Clinicians evaluated relevance and comprehensiveness.

resultsTwelve patients (9 MF, 3 SS) and eight clinician experts (3 oncologists, 4 dermatologists, 1 nurse practitioner) participated. The median age of patients was 68 years (range 36-77); six had early-stage (IA - IIA) disease and six had advanced-stage (IIB - IVB) disease. All items were deemed relevant by at least 95% of participants, and 44 of 47 items achieved 100% relevance across patients and clinicians. All items achieved at least 90% comprehensibility among patients, and 39 of 47 scored items were understood by all patients. All patients found the instructions and response options easy to understand, and all participants considered the instrument comprehensive.

conclusionsThe FACT-CTCL demonstrated strong content validity in this sample of patients with MF/SS and expert clinicians. These findings support further evaluation and use of the FACT-CTCL as a disease-specific HRQoL instrument in MF/SS, while additional study in larger and more diverse populations remains warranted.

Indexed as

Lymphoma, T-Cell, CutaneousMycosis FungoidesPatient Reported Outcome MeasuresQuality of LifeSezary SyndromeSkin NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedQualitative ResearchReproducibility of ResultsSurveys and QuestionnairesContent validityCutaneous T-cell lymphomaFACT-CTCLHealth-related quality of lifeMycosis fungoidesPatient-reported outcomesSézary syndrome

Identifiers

PMID42334715
PMCPMC13554038

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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.