Urothelial carcinoma in situ response to cisplatin-based neoadjuvant chemotherapy, or lack thereof: Impact on patient selection for organ preservation in muscle-invasive disease?

2020 ◽  
Vol 38 (11) ◽  
pp. 850.e1-850.e7
Author(s):  
Isamu Tachibana ◽  
Elhaam Bandali ◽  
Adam C. Calaway ◽  
Naveen Krishnan ◽  
Liang Cheng ◽  
...  
2018 ◽  
Vol 199 (4S) ◽  
Author(s):  
Elhaam Bandali ◽  
Adam Calaway ◽  
Naveen Krishnan ◽  
Clint Cary ◽  
Timothy Masterson ◽  
...  

2018 ◽  
Vol 16 (4) ◽  
pp. e851-e858 ◽  
Author(s):  
Patrick J. Hensley ◽  
Jeffrey Goodwin ◽  
Daniel L. Davenport ◽  
Stephen E. Strup ◽  
Andrew James

2017 ◽  
Vol 15 (4) ◽  
pp. 479-486 ◽  
Author(s):  
Derek E. Thomas ◽  
Hristos Z. Kaimakliotis ◽  
Kevin R. Rice ◽  
Jose A. Pereira ◽  
Paul Johnston ◽  
...  

2014 ◽  
Vol 96 (7) ◽  
pp. e30-e31
Author(s):  
K Murtagh ◽  
R Kockelbergh

We report two cases of bladder contracture following photodynamic or ‘blue light’ detection and cystodiathermy for bladder carcinoma in situ. These patients were unsuitable for treatment with immunotherapy/chemotherapy or had disease recurrence following such treatment. Radical cystectomy was not a treatment option in either patient. Each underwent serial photodynamic cystodiathermy over a three-year period. Neither patient developed muscle invasive disease. However, treatment resulted in contracture of the bladder and incontinence of urine. Patients need to be fully aware of this potential complication in order to make informed choices about their care.


2012 ◽  
Vol 187 (4S) ◽  
Author(s):  
Shabi Ahmad ◽  
Nikhil Vasdev ◽  
John Frew ◽  
Ian Pedley ◽  
Janet Whiteway ◽  
...  

2018 ◽  
Vol 211 (3) ◽  
pp. 712-713 ◽  
Author(s):  
Gitanjali V. Patel ◽  
Eduardo Pascual Van Sant ◽  
Bret Taback ◽  
Richard Ha

Biology ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 109
Author(s):  
Ilan Bejar ◽  
Jacob Rubinstein ◽  
Jacob Bejar ◽  
Edmond Sabo ◽  
Hilla K Sheffer ◽  
...  

Introduction: Our previous studies showed elevated levels of Semaphorin3a (Sema3A) in the urine of patients with urothelial cancer compared to healthy patients. The aim of this study was to analyze the extent of Sema3A expression in normal and malignant urothelial tissue using immune-staining microscopic and morphometric analysis. Materials and Methods: Fifty-seven paraffin-embedded bladder samples were retrieved from our pathology archive and analyzed: 14 samples of normal urothelium, 21 samples containing low-grade urothelial carcinoma, 13 samples of patients with high-grade urothelial carcinoma, 7 samples containing muscle invasive urothelial carcinoma, and 2 samples with pure urothelial carcinoma in situ. All samples were immunostained with anti Sema3A antibodies. The area of tissue stained with Sema3A and its intensity were analyzed using computerized morphometry and compared between the samples’ groups. Results: In normal bladder tissue, very light Sema3A staining was demonstrated on the mucosal basal layer and completely disappeared on the apical layer. In low-grade tumor samples, cells in the basal layer of the mucosa were also lightly stained with Sema3A, but Seama3A expression intensified upon moving apically, reaching its highest level on apical cells exfoliating to the urine. In high grade urothelial tumors, Seama3A staining was intense in the entire thickness of the mucosa. In samples containing carcinoma in situ, staining intensity was high and homogenous in all the neoplastic cells. Conclusions: Sema3A may be serve as a potential non-invasive marker of urothelial cancer.


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