| Literature DB >> 32040781 |
Sunao Shoji1, Shinichiro Hiraiwa2, Izumi Hanada3, Hakushi Kim3, Masahiro Nitta3, Masanori Hasegawa3, Yoshiaki Kawamura3, Kazunobu Hashida4, Takuma Tajiri2, Akira Miyajima3.
Abstract
Multiparametric magnetic resonance imaging (mpMRI) has been increasingly used to diagnose clinically significant prostate cancer (csPC) because of its usefulness in combination with anatomic and functional data. MRI-targeted biopsy, such as MRI-transrectal ultrasound (TRUS) fusion image-guided prostate biopsy, has high accuracy in the detection and localization of csPC. This novel diagnostic technique contributes to the development of tailor-made medicine as focal therapy, which cures the csPC while preserving the anatomical structures related to urinary and sexual function. In the early days of focal therapy, TRUS-guided systematic biopsy was used for patient selection, and treatment was performed for patients with low-risk PC. With the introduction of mpMRI and mapping biopsy, the treatment range is now determined based on individualized cancer localization. In recent prospective studies, 87.4% of treated patients had intermediate- and high-risk PC. However, focal therapy has two main limitations. First, a randomized controlled trial would be difficult to design because of the differences in pathological features between patients undergoing focal therapy and radical treatment. Therefore, pair-matched studies and/or historical controlled studies have been performed to compare focal therapy and radical treatment. Second, no long-term (≥ 10-year) follow-up study has been performed. However, recent prospective studies have encouraged the use of focal therapy as a treatment strategy for localized PC because it contributes to high preservation of continence and erectile function.Entities:
Keywords: Focal therapy; Magnetic resonance imaging–transrectal ultrasound fusion image-guided prostate biopsy; Multi-parametric magnetic resonance imaging; Prostate cancer
Mesh:
Year: 2020 PMID: 32040781 DOI: 10.1007/s10147-020-01627-8
Source DB: PubMed Journal: Int J Clin Oncol ISSN: 1341-9625 Impact factor: 3.402