The goal of this observational study is to evaluate whether body composition abnormalities (sarcopenia, myosteatosis, and obesity) and nutritional status influence the risk of recurrence and progression in adult patients with non-muscle-invasive bladder cancer (NMIBC). The main questions it aims to answer are: Do sarcopenia, myosteatosis, obesity, or malnutrition increase the likelihood of NMIBC recurrence and progression? Can clinical, laboratory, and CT-derived body composition parameters serve as predictive biomarkers that improve individualized risk stratification? Participants will undergo routine clinical and radiologic assessments, including: * completion of the SARC-F and NRS nutritional screening questionnaires * anthropometric measurements (BMI, waist circumference) * laboratory evaluation including serum albumin and testosterone * CT-based assessment of skeletal muscle index (SMI) and muscle density (SMD) * standard TURBT and structured follow-up with cystoscopy, cytology, imaging, and clinical evaluations to document recurrence and progression.
Non-muscle-invasive bladder cancer (NMIBC) accounts for approximately 75% of bladder cancer cases and is characterized by a high rate of recurrence and a variable risk of progression. Existing prognostic models, such as EAU and EORTC calculators, incorporate tumor-specific features but do not consider patient-related factors such as body composition or nutritional status. Emerging evidence suggests that sarcopenia, myosteatosis, obesity, and malnutrition may adversely influence oncologic outcomes through mechanisms involving systemic inflammation, impaired immune response, metabolic dysfunction, and reduced physiological reserve. These host-related factors may therefore represent important, yet under-recognized, prognostic biomarkers in NMIBC. This prospective observational cohort study aims to determine whether clinical and radiologic measures of body composition and nutritional status are associated with the risk of recurrence and progression in patients with NMIBC. Preoperative assessment will include SARC-F screening for sarcopenia, NRS screening for nutritional risk, anthropometric measurements (BMI and waist circumference), serum albumin and testosterone measurement, and CT-based quantification of skeletal muscle index (SMI) and skeletal muscle density (SMD). Tumor-related variables including stage, grade, presence of carcinoma in situ, variant histology, lymphovascular invasion, and tumor size and multiplicity will be abstracted from pathology and clinical records. All participants will undergo standard transurethral resection of bladder tumor (TURBT), and postoperative management will follow guideline-recommended NMIBC surveillance schedules based on individual EAU/EORTC risk stratification. During follow-up, patients will undergo regular cystoscopic evaluations, urine cytology, serial SARC-F and NRS assessments, anthropometric measurements, albumin monitoring, and periodic CT imaging to reassess SMI and SMD. Recurrence and progression events will be documented according to standard clinical criteria. By identifying clinically meaningful host-related predictors of recurrence and progression, this study may improve individualized risk stratification, inform tailored surveillance strategies, and highlight the need for early identification and correction of adverse body composition and nutritional states in patients with NMIBC.
Study Type
OBSERVATIONAL
Enrollment
150
Progression-Free Survival (PFS)
Time from TURBT to progression to muscle-invasive bladder cancer (≥ T2) or other defined progression endpoints (CIS emergence, variant histology progression).
Time frame: Up to 36 months
Recurrence-Free Survival (RFS)
Time from transurethral resection of bladder tumor (TURBT) to the first documented recurrence of non-muscle-invasive bladder cancer, confirmed by cystoscopy, urine cytology, or pathology.
Time frame: Up to 36 months
Impact of Preoperative Skeletal Muscle Index (SMI) on Recurrence Free Survival (RFS)
Recurrence-free survival according to skeletal muscle index (SMI) measured on baseline computed tomography (CT) images at L3 level (cm²/m²).
Time frame: baseline to 36 months
Impact of Preoperative Skeletal Muscle Density (SMD) on Recurrence Free Survival (RFS)
Recurrence-free survival according to skeletal muscle density (SMD) measured in Hounsfield units (HU) on baseline computed tomography (CT) images at L3 level
Time frame: baseline to 36 months
Impact of Preoperative Body Mass Index (BMI) on Recurrence Free Survival (RFS)
Recurrence-free survival according to body mass index (BMI) measured at the baseline evaluation (kg/m²)
Time frame: baseline to 36 months
Impact of Preoperative Nutritional Risk Score (NRS 2002) on Recurrence Free Survival (RFS)
Recurrence-free survival according to Nutritional Risk Score (NRS 2002) assesed at the baseline evaluation (expressed in points using the standardized NRS-2002 questionnaire)
Time frame: baseline to 36 months
Overall Survival (OS)
Time from TURBT to death from any cause.
Time frame: Up to 36 months
Cancer-Specific Survival (CSS)
Time from TURBT to death specifically attributed to bladder cancer.
Time frame: Up to 36 months
Impact of Preoperative Skeletal Muscle Index (SMI) on Progression Free Survival (PFS)
Progression-free survival according to skeletal muscle index (SMI) measured on baseline computed tomography (CT) images at L3 level (cm²/m²).
Time frame: baseline to 36 months
Impact of Preoperative Skeletal Muscle Density (SMD) on Progression Free Survival (PFS)
Progression-free survival according to skeletal muscle density (SMD) measured in Hounsfield units (HU) on baseline computed tomography (CT) images at L3 level
Time frame: baseline to 36 months
Impact of Preoperative Body Mass Index (BMI) on Progression Free Survival (PFS)
Progression-free survival according to body mass index (BMI) measured at the baseline evaluation (kg/m²)
Time frame: baseline to 36 months
Impact of Preoperative Nutritional Risk Score (NRS 2002) on Progression Free Survival (PFS)
Progression-free survival according to Nutritional Risk Score (NRS 2002) assesed at the baseline evaluation (expressed in points using the standardized NRS-2002 questionnaire)
Time frame: baseline to 36 months
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