TY - JOUR
T1 - Development and psychometric evaluation of a patient-reported symptom index for patients with non-muscle invasive bladder cancer: the NMIBC-SI
AU - Rutherford, Claudia
AU - Tait, Margaret-Ann
AU - Costa, Daniel S. J.
AU - King, Madeleine T.
AU - Smith, David P.
AU - Sengupta, Shomik
AU - Ischia, Joseph
AU - Mitterdorfer, Andrew
AU - Hayne, Dickon
AU - Watson, Roger
AU - Anderson, Paul
AU - Frydenberg, Mark
AU - Gilling, Peter
AU - Buchan, Nicholas
AU - Green, Euan
AU - Clarke, Noel
AU - Boorjian, Stephen A.
AU - Konety, Badrinath
AU - Holzbeierlein, Jeffrey M.
AU - Black, Peter C.
AU - Chalasani, Venu
AU - Henseler, Jörg
AU - Patel, Manish I.
PY - 2025/3/27
Y1 - 2025/3/27
N2 - Background and objective: Non-muscle invasive bladder cancer (NMIBC) is a chronic condition requiring frequent follow-up with endoscopic examinations, tumour resections and intravesical treatments. In this clinical context, patient-reported outcomes (PROs) have enormous potential to inform treatment assessment and recommendations for NMIBC. We aimed to develop and evaluate a patient-reported NMIBC Symptom Index (NMIBC-SI) to facilitate clinical research and enhance care. Methods: NMIBC-SI items were developed based on existing literature and qualitative interviews with patients and clinicians, and evaluated in two field tests: item reduction, using NMIBC-SI data from 220 patients on active treatment from nine Australian centres; reliability and validity evaluation of item-reduced version using NMIBC-SI data from 232 patients from five countries. Results: NMIBC-SI assesses disease and treatment-related symptom burden and two treatment-specific side-effects (cystoscopy, intravesical BCG/Chemotherapy). Composite analysis supported a single composite model including core symptom and cystoscopy index items (Intravesical index items were not tested due to small sample). Test-retest reliability was strong (range 0.894–0.91). As expected, the NMIBC-SI was able to discriminate between no treatment and any treatment groups, and no treatment and chemo/BCG groups, providing evidence towards validity. Conclusions and clinical implications: NMIBC-SI assesses patients’ self-reported symptom burden and can be used to evaluate NMIBC treatments from the perspective of patients. The NMIBC-SI is acceptable to patients and has evidence for reliability and validity. Future validation work with patients with greater symptom burden is warranted.
AB - Background and objective: Non-muscle invasive bladder cancer (NMIBC) is a chronic condition requiring frequent follow-up with endoscopic examinations, tumour resections and intravesical treatments. In this clinical context, patient-reported outcomes (PROs) have enormous potential to inform treatment assessment and recommendations for NMIBC. We aimed to develop and evaluate a patient-reported NMIBC Symptom Index (NMIBC-SI) to facilitate clinical research and enhance care. Methods: NMIBC-SI items were developed based on existing literature and qualitative interviews with patients and clinicians, and evaluated in two field tests: item reduction, using NMIBC-SI data from 220 patients on active treatment from nine Australian centres; reliability and validity evaluation of item-reduced version using NMIBC-SI data from 232 patients from five countries. Results: NMIBC-SI assesses disease and treatment-related symptom burden and two treatment-specific side-effects (cystoscopy, intravesical BCG/Chemotherapy). Composite analysis supported a single composite model including core symptom and cystoscopy index items (Intravesical index items were not tested due to small sample). Test-retest reliability was strong (range 0.894–0.91). As expected, the NMIBC-SI was able to discriminate between no treatment and any treatment groups, and no treatment and chemo/BCG groups, providing evidence towards validity. Conclusions and clinical implications: NMIBC-SI assesses patients’ self-reported symptom burden and can be used to evaluate NMIBC treatments from the perspective of patients. The NMIBC-SI is acceptable to patients and has evidence for reliability and validity. Future validation work with patients with greater symptom burden is warranted.
UR - http://www.scopus.com/inward/record.url?scp=105002036867&partnerID=8YFLogxK
U2 - 10.1186/s41687-025-00864-7
DO - 10.1186/s41687-025-00864-7
M3 - Article
SN - 2509-8020
VL - 9
JO - Journal of Patient-Reported Outcomes
JF - Journal of Patient-Reported Outcomes
IS - 1
M1 - 36
ER -