scholarly journals Application of pirarubicin photosensitizer fluorescence cystoscopy in early detection of bladder cancer

2017 ◽  
Vol 14 (3) ◽  
pp. 3309-3312 ◽  
Author(s):  
Bo Jiang ◽  
Yang Dong ◽  
Houguang He ◽  
Conghui Han
2009 ◽  
Vol 181 (4) ◽  
pp. 603
Author(s):  
Cesare M Scoffone ◽  
Massimiliano Poggio ◽  
Cecilia Maria Cracco ◽  
Marco Cossu ◽  
Davide Vaccino ◽  
...  

2004 ◽  
Vol 171 (4S) ◽  
pp. 73-73 ◽  
Author(s):  
Christoph Durek ◽  
Sigrid Wagner ◽  
Bram Zeijlemaker ◽  
Jeroen Van Moorselaar ◽  
J. Alfred Witjes ◽  
...  

2018 ◽  
Vol 199 (4S) ◽  
Author(s):  
Simeon Springer ◽  
Maria Del Carmen Rodriguez Pena ◽  
Aline Tregnago ◽  
Diana Taheri ◽  
Stephania Bezerra ◽  
...  

2019 ◽  
Vol 37 (18) ◽  
pp. 1547-1557 ◽  
Author(s):  
Emil Christensen ◽  
Karin Birkenkamp-Demtröder ◽  
Himanshu Sethi ◽  
Svetlana Shchegrova ◽  
Raheleh Salari ◽  
...  

PURPOSE Novel sensitive methods for early detection of relapse and for monitoring therapeutic efficacy may have a huge impact on risk stratification, treatment, and ultimately outcome for patients with bladder cancer. We addressed the prognostic and predictive impact of ultra-deep sequencing of cell-free DNA in patients before and after cystectomy and during chemotherapy. PATIENTS AND METHODS We included 68 patients with localized advanced bladder cancer. Patient-specific somatic mutations, identified by whole-exome sequencing, were used to assess circulating tumor DNA (ctDNA) by ultra-deep sequencing (median, 105,000×) of plasma DNA. Plasma samples (n = 656) were procured at diagnosis, during chemotherapy, before cystectomy, and during surveillance. Expression profiling was performed for tumor subtype and immune signature analyses. RESULTS Presence of ctDNA was highly prognostic at diagnosis before chemotherapy (hazard ratio, 29.1; P = .001). After cystectomy, ctDNA analysis correctly identified all patients with metastatic relapse during disease monitoring (100% sensitivity, 98% specificity). A median lead time over radiographic imaging of 96 days was observed. In addition, for high-risk patients (ctDNA positive before or during treatment), the dynamics of ctDNA during chemotherapy was associated with disease recurrence ( P = .023), whereas pathologic downstaging was not. Analysis of tumor-centric biomarkers showed that mutational processes (signature 5) were associated with pathologic downstaging ( P = .024); however, no significant correlation for tumor subtypes, DNA damage response mutations, and other biomarkers was observed. Our results suggest that ctDNA analysis is better associated with treatment efficacy compared with other available methods. CONCLUSION ctDNA assessment for early risk stratification, therapy monitoring, and early relapse detection in bladder cancer is feasible and provides a basis for clinical studies that evaluate early therapeutic interventions.


2012 ◽  
Vol 53 (12) ◽  
pp. 821 ◽  
Author(s):  
Jae Seung Lee ◽  
Seo Yeon Lee ◽  
Woo Jung Kim ◽  
Seong Il Seo ◽  
Seong Soo Jeon ◽  
...  

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