4.0 Article

A Randomized Feasibility Trial Comparing Surveillance Regimens for Patients with Low and Low-Intermediate Risk Non-Muscle Invasive Bladder Cancer

Journal

BLADDER CANCER
Volume 7, Issue 3, Pages 285-295

Publisher

IOS PRESS
DOI: 10.3233/BLC-201535

Keywords

Bladder cancer; surveillance; recurrence; quality of life

Funding

  1. NIH [T32GM113896]
  2. NIA [T32 AG 021890]
  3. Mays Family Cancer Center at University of Texas Health San Antonio [P30 CA054174]
  4. Roger L. And Laura D. Zeller Charitable Foundation Chair in Urologic Cancer [CDMRP CA170270/P1P2]
  5. Max & Minnie Tomerlin Voelcker Fund
  6. NIH/NCATS [TL1 TR002647]
  7. [8KL2 TR000118]

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The study found challenges in randomizing patients to different surveillance frequencies for non-muscle invasive bladder cancer. Patient willingness to participate was high, but 35.7% declined enrollment due to preference for high frequency surveillance. There were no significant differences in disease recurrence, comfort, and quality of life between patients in the high frequency and low frequency groups, but the high frequency group had higher annual out-of-pocket costs and healthcare system costs.
BACKGROUND: Surveillance regimens for non-muscle invasive bladder cancer (NMIBC) are disparate and controlled trials could inform guidelines. The feasibility of randomizing patients to variable frequency surveillance is unknown. OBJECTIVES: To determine patient willingness to randomization to high frequency (HF) versus low frequency (LF) surveillance regimen for NMIBC and compare patient comfort and healthcare costs across regimens. METHODS: A non-blinded, two-arm, randomized-controlled study of patients with low or low-intermediate risk NMIBC was conducted at two institutions where patients were offered randomization to HF vs. LF surveillance following initial tumor resection. The HF group underwent cystoscopy every three months for 2 years, then every 6 months for 2 years, then annually. The LF group underwent cystoscopy at 9 months following the 3-month cystoscopy, then annually. Assuming 75% of patients approached would agree to enrollment, a sample size of n = 35 patients per arm provided a one-sided 95% exact Clopper-Pearson confidence lower-limit of 60%. RESULTS: Of 70 patients approached, 45 (64.3%) agreed to participate and 25 (35.7%) declined enrollment due to preference for HF. Twelve biopsies were performed, including 4 (19%) of 21 patients in the HF group and 8 (33.3%) of 24 patients in the LF group. Disease recurrence (low grade Ta) was observed in 3 (14.3%) and 5 (20.8%) patients in the HF and LF groups, respectively. No patients experienced high grade recurrence or progression. Both groups had similar patient-reported procedure-related discomfort and quality of life measures over time. Patient out-of-pocket cost and healthcare systems costs were $383.80 more per patient annually in the HF group. CONCLUSIONS: Randomization to variable frequency surveillance is challenging as over a third of patients declined participation. However, these data provide important preliminary insights into the potential effects of surveillance frequency on oncologic and economic outcomes in patients with low and low-intermediate risk bladder cancer.

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