scholarly journals Standardization of definitions in focal therapy of prostate cancer: report from a Delphi consensus project

2016 ◽  
Vol 34 (10) ◽  
pp. 1373-1382 ◽  
Author(s):  
A. W. Postema ◽  
T. M. De Reijke ◽  
O. Ukimura ◽  
W. Van den Bos ◽  
A. R. Azzouzi ◽  
...  
2015 ◽  
Vol 33 (10) ◽  
pp. 1503-1509 ◽  
Author(s):  
B. G. Muller ◽  
W. van den Bos ◽  
M. Brausi ◽  
J. J. Fütterer ◽  
S. Ghai ◽  
...  

2015 ◽  
Vol 14 (2) ◽  
pp. e829-e829b
Author(s):  
B.G. Muller ◽  
W. Van Den Bos ◽  
M. Brausi ◽  
J.J. Fütterer ◽  
S. Ghai ◽  
...  

2014 ◽  
Vol 114 (5) ◽  
pp. 698-707 ◽  
Author(s):  
Berrend G. Muller ◽  
Willemien van den Bos ◽  
Maurizio Brausi ◽  
Francois Cornud ◽  
Paolo Gontero ◽  
...  

2016 ◽  
Vol 15 (3) ◽  
pp. e834
Author(s):  
A. Postema ◽  
T. De Reijke ◽  
O. Ukimura ◽  
W. Van Den Bos ◽  
J. De La Rosette

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Yu Wang ◽  
Al Christopher De Leon ◽  
Reshani Perera ◽  
Eric Abenojar ◽  
Ramamurthy Gopalakrishnan ◽  
...  

AbstractUltrasound imaging is routinely used to guide prostate biopsies, yet delineation of tumors within the prostate gland is extremely challenging, even with microbubble (MB) contrast. A more effective ultrasound protocol is needed that can effectively localize malignancies for targeted biopsy or aid in patient selection and treatment planning for organ-sparing focal therapy. This study focused on evaluating the application of a novel nanobubble ultrasound contrast agent targeted to the prostate specific membrane antigen (PSMA-targeted NBs) in ultrasound imaging of prostate cancer (PCa) in vivo using a clinically relevant orthotopic tumor model in nude mice. Our results demonstrated that PSMA-targeted NBs had increased extravasation and retention in PSMA-expressing orthotopic mouse tumors. These processes are reflected in significantly different time intensity curve (TIC) and several kinetic parameters for targeted versus non-targeted NBs or LUMASON MBs. These, may in turn, lead to improved image-based detection and diagnosis of PCa in the future.


2019 ◽  
Vol 36 (05) ◽  
pp. 351-366
Author(s):  
David A. Woodrum ◽  
Akira Kawashima ◽  
Krzysztof R. Gorny ◽  
Lance A. Mynderse

AbstractIn 2019, the American Cancer Society (ACS) estimates that 174,650 new cases of prostate cancer will be diagnosed and 31,620 will die due to the prostate cancer in the United States. Prostate cancer is often managed with aggressive curative intent standard therapies including radiotherapy or surgery. Regardless of how expertly done, these standard therapies often bring significant risk and morbidity to the patient's quality of life with potential impact on sexual, urinary, and bowel functions. Additionally, improved screening programs, using prostatic-specific antigen and transrectal ultrasound-guided systematic biopsy, have identified increasing numbers of low-risk, low-grade “localized” prostate cancer. The potential, localized, and indolent nature of many prostate cancers presents a difficult decision of when to intervene, especially within the context of the possible comorbidities of aggressive standard treatments. Active surveillance has been increasingly instituted to balance cancer control versus treatment side effects; however, many patients are not comfortable with this option. Although active debate continues on the suitability of either focal or regional therapy for the low- or intermediate-risk prostate cancer patients, no large consensus has been achieved on the adequate management approach. Some of the largest unresolved issues are prostate cancer multifocality, limitations of current biopsy strategies, suboptimal staging by accepted imaging modalities, less than robust prediction models for indolent prostate cancers, and safety and efficiency of the established curative therapies following focal therapy for prostate cancer. In spite of these restrictions, focal therapy continues to confront the current paradigm of therapy for low- and even intermediate-risk disease. It has been proposed that early detection and proper characterization may play a role in preventing the development of metastatic disease. There is level-1 evidence supporting detection and subsequent aggressive treatment of intermediate- and high-risk prostate cancer. Therefore, accurate assessment of cancer risk (i.e., grade and stage) using imaging and targeted biopsy is critical. Advances in prostate imaging with MRI and PET are changing the workup for these patients, and advances in MR-guided biopsy and therapy are propelling prostate treatment solutions forward faster than ever.


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