Producing a Novel Symptom Burden Scale for People Living With Idiopathic Multicentric Castleman Disease (ISBUS)

Development, validation of a novel symptom burden scale to assess and quantify the burden experienced by people living with Idiopathic Multicentric Castleman Disease (iMCD).

Study Overview

• Status: Not yet recruiting
• Conditions: Idiopathic Multicentric Castleman's Disease
• Intervention / Treatment: Other: Research questions

Detailed Description

Idiopathic Multicentric Castleman Disease (iMCD) is a rare lymphoproliferative disorder associated with systemic inflammation and organ dysfunction. The condition has an unknown aetiology and diagnostic criteria were established recently in 2017. It can be distinguished from other forms of Castleman Disease, including unicentric presentations and Multicentric Castleman Disease (MCD) that is associated with the Kaposi sarcoma herpesvirus. iMCD has an estimated prevalence of between 6.9 and 9.7 people per million. While clinical presentations vary, iMCD can be associated with a high degree of symptom burden, including constitutional, gastrointestinal, neuropsychiatric, dermatologic, respiratory, and hematologic or lymphoreticular problems. Both symptoms and the side-effects of treatment can impact the health-related quality of life (HRQoL) of people with iMCD

This international mixed-methods study will be conducted in four stages:

Stage 1: Item generation

• Drawing on the content, data, and analysis from a previous international patient online survey in iMCD with 65 patients, generate draft PROM content (including a longlist of candidate draft items under existing themes) to assess symptom burden in iMCD.
• Incorporate expert opinion and lived experience to achieve consensus on which items will be tested for inclusion in the symptom burden scale via an online multi-stakeholder workshop involving the funder, research team, patient and public involvement and engagement (PPIE) representative(s) (i.e., patients with iMCD and/or their carers), healthcare professionals, and any other relevant stakeholders.

Stage 2: Item testing and refinement

• Cognitive debriefing interviews with about 10 people living with iMCD to assess the content validity of the items (and associated PROM content) in terms of relevance, comprehensibility, and comprehensiveness. This will include assessing whether they are important/meaningful to patients.
• Analyse and summarise qualitative evidence on content validity, make recommendations on revisions to the draft PROM, and agree this with the multi-stakeholder advisory group (as described above) and a separate group of PPIE collaborators.

Stage 3: Final item selection

• Administer the refined PROM (from Stage 2) to as wide a sample as possible of people living with iMCD. The estimated sample size is 100 patients. The PROM will be administered alongside additional sociodemographic and clinical questions and measures of burden and/or health-related quality of life (HRQoL).
• Taking into account the sample size, conduct appropriate psychometric analyses in order to provide evidence for final item selection and to provide preliminary psychometric evidence on the reliability and validity of the final measure.
• Taking into account all of the available qualitative and quantitative evidence, and a consultation with PPIE collaborators, agree (with the multi-stakeholder advisory group) on final item selection, with the goal of obtaining an 8-10 item measure of symptom burden.

Stage 4: Preliminary measures of change

• Stage 4a: Re-administer the refined PROM (from Stage 2) to participants (from Stage 3) alongside measure(s) of perceived clinical change.
• Stage 4b: Conduct qualitative interviews with about 10 participants who have completed the PROM at both time points to understand what constitutes a meaningful difference from their perspective.
• Triangulate quantitative and qualitative data to estimate a minimally important clinical difference (MCID) for the new PROM, agreed with the multi-stakeholder advisory group.

Recruitment for Stages 2-4 will take place in USA, Canada, Brazil, Australia, New Zealand and the United Kingdom. Interviews will be conducted online for Stages 2 and 4 and the psychometric survey will be hosted and administered online.

Governance: The results of each stage will be discussed and final decisions will be made with a multi-stakeholder group consisting of the wider research team, clinicians and other healthcare professionals and PPIE.

• Study Type: Observational
• Enrollment (Estimated): 100

Contacts and Locations

• Study Contact: Name: Anju Keetharuth, PhD; Phone Number: +44 (0) 114 222 0884; Email: d.keetharuth@sheffield.ac.uk
• Study Contact Backup: Name: Philip Powell, PhD; Phone Number: +44 (0) 114 222 0794; Email: p.a.powell@sheffield.ac.uk

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

• Sampling Method: Non-Probability Sample

Study Population

Adult patients diagnosed with idiopathic Multicentric Castleman Disease (iMCD).

Description

Inclusion Criteria:

• Diagnosis of idiopathic Multicentric Castleman Disease (iMCD)
• Adults (aged 18+ years)
• Fluent in English

Exclusion Criteria:

• No diagnosis of iMCD
• Children (aged < 18 years)
• Not able to understand or communicate in English
• People lacking the capacity to consent

Study Plan

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Long list of candidate items for the scale (stage 1)	completion of data analysis from a previous survey	Sept 2023 - Nov 2023
Completion of interviews (stage 2)	completion of interviews by 10 patients from all recruiting sites	Within 6 months from start (With this being a rare condition, data from all patients will be collected at various levels of treatment and time from diagnosis)
Completion of interviews (stage 4b)	completion of interviews by 10 patients from all recruiting sites	About 4 weeks after Stage 4a
Completion of questionnaire (stage 3)	completion of questionnaire which includes extra questions about treatments, time of diagnosis. Completion of EQ-5D for external validity of PROM. NB: EQ-5D is the full name of the instrument and not an acronym.	Within 9 months from start (With this being a rare condition, data from all patients will be collected at various levels of treatment and time from diagnosis). NB: Advisory comments noted.
Completion of follow-up questionnaire (stage 4a)	completion of follow-up questionnaire from Stage 3 by same patients who participated in Stage 3. Note: The full name of the scale will be discussed and confirmed. At the moment, the working title is Idiopathic Multicentric Castleman Disease Symptom Burden Scale (ISBUS).	About 8 weeks after Stage 3 questionnaire. Note: Advisory comments noted.

Collaborators and Investigators

• Sponsor: EusaPharma (UK) Limited
• Collaborators: University of Sheffield (ScHARR); KMC Health Care; Castleman Disease Collaborative Network (CDCN)
• Investigators: Principal Investigator: Anju Keetharuth, PhD, University of Sheffield; Principal Investigator: Philip Powell, PhD, University of Sheffield

Publications and helpful links

Helpful Links

• example of registration of PROMs
• example of registration of PROMs
• example of registration of PROMs

Study record dates

Study Major Dates

• Study Start (Estimated): October 1, 2023
• Primary Completion (Estimated): December 1, 2024
• Study Completion (Estimated): December 1, 2024

Study Registration Dates

• First Submitted: July 26, 2023
• First Submitted That Met QC Criteria: August 10, 2023
• First Posted (Actual): August 16, 2023

Study Record Updates

• Last Update Posted (Actual): August 22, 2023
• Last Update Submitted That Met QC Criteria: August 17, 2023
• Last Verified: August 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Immune System Diseases; Lymphoproliferative Disorders; Lymphatic Diseases; Immunoproliferative Disorders; Castleman Disease
• Other Study ID Numbers: ISBUS

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO
• IPD Plan Description: Deanonymized transcriptions of stages 2 and 4 interviews will be securely stored in the University of Sheffield repository with access restricted to investigators only. Quantitative data from stages 3 and 4a will be processed, stored and accessed similarly in the same location.

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No