Quality of life assessment during prostate cancer radionuclide therapy: Updated FACT-RNT psychometric evaluation.
Abstract
141 Background: The Functional Assessment of Cancer Therapy–Radionuclide Therapy (FACT-RNT) is a 15-item patient-reported outcome (PRO) measure used to monitor RNT-related symptoms, toxicities, and quality-of-life impacts in patients with metastatic castrate-resistant prostate cancer (mCRPC). This study re-examined the validity and reliability of the FACT-RNT using repeated assessments in an expanded, multi-institutional cohort of patients receiving RNT. Methods: Patients starting 177 Lu-PSMA-617 for mCRPC at UCLA from December 2022 to August 2023 and at Moffitt Cancer Center from October 2023 to October 2025 completed the FACT-RNT before each cycle. Patients at Moffitt also completed previously validated measures of prostate cancer disease- and treatment-related symptoms (NFPSI-17) and physical function (PG-SGA). Reliability was assessed through tests of internal consistency, split-half reliability, inter-item correlations, and test-retest reliability across RNT cycles 1-4. Correlations between the FACT-RNT and both the NFPSI-17 and PG-SGA at cycle 2 were calculated to assess convergent validity. Results: Patients (N=81) were predominantly non-Hispanic (80%) and White (69%), and were, on average, 70 years old (SD=9, range=43-91) at RNT cycle 1. Fifty-nine (73%) completed the FACT-RNT for ≥2 cycles, and 33 (41%) completed the FACT-RNT for ≥4 cycles. Internal consistency reliability across cycles was good-to-excellent (α=0.83-0.90), average split-half reliabilities were excellent (α=0.82-0.86), and average inter-item correlations were acceptable ( r =0.24-0.30). Test-retest reliability was moderate-to-good for individual cycle scores (ICC3,1=0.68, CI=0.53-0.81, p<0.001) and excellent when averaging across cycles 1-4 (ICC3,4=0.89, CI=0.82-0.94, p<0.001). FACT-RNT total score correlations between consecutive cycles were also strong (cycles 2-3, r =0.72; cycles 3-4, r =0.91). For patients completing other PROs at cycle 2 (n=23), the FACT-RNT was positively associated with symptoms as assessed by NFPSI-17 ( r =0.89, p <0.001) and negatively associated with physical functioning assessed by PG-SGA ( r =-0.61, p <0.002), suggesting strong convergent validity. Conclusions: Results from updated analyses suggest that the FACT-RNT has good-to-excellent internal consistency and split-half reliability, acceptable inter-item correlations, and moderate-to-excellent stability across administrations. As between-cycle variability in treatment-related symptoms is expected, these findings may reflect both true change in treatment-related symptoms and quality of life, and measurement reliability. The FACT-RNT also correlated as expected with related PRO measures, supporting preliminary convergent validity. Overall, this evidence supports the validity and reliability of the FACT-RNT and its use in future research and clinical practice.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (15)
KD L. Jacobs
H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL
Bihe Hu
H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL
Lisa Marie Gudenkauf
Brigham and Women's Hospital, Boston, MA
Xiaoyin Li
Heather S.L. Jim
H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL
Laura B. Oswald
H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL
Vishnu Murthy
University of California, Los Angeles, Los Angeles, CA
Ethan C. Lam
University of California, Los Angeles, Los Angeles, CA
Linda Gardner
University of California, Los Angeles, Los Angeles, CA
Adam P. Dicker
Johannes Czernin
Ahmanson Translational Theranostics Division, University of California, Los Angeles, Los Angeles, CA
David Cella
Ghassan El-Haddad
H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL
Jeremie Calais
Luca F. Valle, MD, Department of Radiation Oncology, University of California Los Angeles, Los Angeles, CA, Radiation Oncology Service, Greater Los Angeles VA Healthcare System, Los Angeles, CA, University of California Los Angeles Jonsson Comprehensive Cancer Center, Los Angeles, CA, Jeremie Calais, MD, PhD, University of California Los Angeles Jonsson Comprehensive Cancer Center, Los Angeles, CA, Department of Nuclear Medicine, University of California Los Angeles, Los Angeles, CA, Amar U. Kishan, MD, Department of Radiation Oncology, University of California Los Angeles, Los Angeles, CA, University of California Los Angeles Jonsson Comprehensive Cancer Center, Los Angeles, CA
Brian D. Gonzalez