1050 FDG-PET/CT improves staging in patients with high-risk muscle-invasive bladder cancer scheduled for radical cystectomy

2015 ◽  
Vol 14 (2) ◽  
pp. e1050
Author(s):  
Kollberg P. Johansson ◽  
H. Almquist ◽  
K. Lyttkens ◽  
C. Cronberg ◽  
S. Garpered ◽  
...  
Author(s):  
Pauline Bertolaso ◽  
Véronique Brouste ◽  
Anne-Laure Cazeau ◽  
Henri de Clermont-Gallerande ◽  
Franck Bladou ◽  
...  

2013 ◽  
Vol 12 (1) ◽  
pp. e480
Author(s):  
M.C. Ferriero ◽  
G. Simone ◽  
R. Papalia ◽  
S. Guaglianone ◽  
R. Sciuto ◽  
...  

2018 ◽  
Vol 199 (4S) ◽  
Author(s):  
Muhammad Abdus Salam ◽  
Mir Ehteshamul Haque ◽  
Faisal Islam ◽  
Kaiser Ibrahim ◽  
Shahinul Islam ◽  
...  

Diagnostics ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 863
Author(s):  
Vincenzo Cuccurullo ◽  
Giuseppe Danilo Di Stasio ◽  
Francesco Manti ◽  
Pierpaolo Arcuri ◽  
Rocco Damiano ◽  
...  

Diagnostic imaging in bladder cancer plays an important role since it is needed from pretreatment staging to follow-up, but a morphological evaluation performed with both CT and MRI showed low sensitivities and specificities in detecting pathologic lymph nodes, due to the occurrence of false positive results. Implementation of functional information provided by PET/CT could be a determinant in the management of patients with muscle-invasive bladder cancer. A focus on the role of 18F-FDG PET/CT and alternative tracers in patients with muscle-invasive bladder cancer is provided in this analysis in order to outline its potential applications in staging settings and response evaluation after neoadjuvant chemotherapy.


BMJ Open ◽  
2017 ◽  
Vol 7 (8) ◽  
pp. e017913 ◽  
Author(s):  
Jamie B Oughton ◽  
Heather Poad ◽  
Maureen Twiddy ◽  
Michelle Collinson ◽  
Victoria Hiley ◽  
...  

IntroductionHigh-risk non-muscle invasive bladder cancer (HRNMIBC) is a heterogeneous disease that can be difficult to predict. While around 25% of cancers progress to invasion and metastases, the remaining majority of tumours remain within the bladder. It is uncertain whether patients with HRNMIBC are better treated with intravesical maintenance BCG (mBCG) immunotherapy or primary radical cystectomy (RC). A definitive randomised controlled trial (RCT) is needed to compare these two different treatments but may be difficult to recruit to and has not been attempted to date. Before undertaking such an RCT, it is important to understand whether such a comparison is possible and how best to achieve it.Methods and analysisBRAVO is a multi-centre, parallel-group, mixed-methods, individually randomised, controlled, feasibility study for patients with HRNMIBC. Participants will be randomised to receive either mBCG immunotherapy or RC. The primary objective is to assess the feasibility and acceptability of performing the definitive phase III trial via estimation of eligibility and recruitment rates, assessing uptake of allocated treatment and compliance with mBCG, determining quality-of-life questionnaire completion rates and exploring reasons expressed by patients for declining recruitment into the study. We aim to recruit 60 participants from six centres in the UK. Surgical trials with disparate treatment options find recruitment challenging from both the patient and clinician perspective. By building on the experiences of other similar trials through implementing a comprehensive training package aimed at clinicians to address these challenges (qualitative substudy), we hope that we can demonstrate that a phase III trial is feasible.Ethics and disseminationThe study has ethical approval (16/YH/0268). Findings will be made available to patients, clinicians, the funders and the National Health Service through traditional publishing and social media.Trial registration numberISRCTN12509361; Pre results.


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