Author/Authors :
Schmitz-Dr?ger، نويسنده , , Bernd J. and Todenh?fer، نويسنده , , Tilman and van Rhijn، نويسنده , , Bas and Pesch، نويسنده , , Beate and Hudson، نويسنده , , M?iss A. and Chandra، نويسنده , , Ashish and Ingersoll، نويسنده , , Molly A. and Kassouf، نويسنده , , Wassim and Palou، نويسنده , , Joan and Taylor، نويسنده , , John and Vlahou، نويسنده , , Antonia and Behrens، نويسنده , , Thomas and Critelli، نويسنده , , Rossana and Grossman، نويسنده , , H. Barton and Sanchez-Carbayo، نويسنده , , Marta and Kamat، نويسنده , , Ashish، نويسنده ,
Abstract :
AbstractObjectives
olecular assays for bladder cancer diagnosis and surveillance have been developed over the past several decades. However, none of these markers have been routinely implemented into clinical decision making. Beyond their potential for screening high-risk populations, urine markers likely have the greatest potential in the follow-up of patients with non–muscle invasive bladder cancer (NMIBC).
s
we discuss the current options and limitations of the use of urine markers for patient surveillance, focusing on patients with low-/intermediate-risk NMIBC.
s
se patients have a very low risk of tumor progression, the primary goal of surveillance is detection of recurrent disease. Although urine cytology seems to be limited to detection of few patients who would develop high-grade tumors, we conclude that the use of markers with high sensitivity for low-grade disease for patient follow-up has the potential to decrease the frequency of urethrocystoscopy without compromising patient prognosis. Because a single marker may not have sufficient sensitivity for detection of low-grade tumors, different scenarios, e.g., multitesting and reflex or sequential approaches, are discussed.
sions
is consensus that currently available markers have the potential to support clinical decision making in follow-up of patients with low-/intermediate-risk NMIBC. In light of our analysis, further additional randomized controlled studies to effectively assess the clinical usefulness of modern urine markers are required.
Keywords :
Urine markers , Non–muscle invasive bladder cancer , disease management , costs , Low risk