Abstract 272P
Background
Prostate cancer was the second most commonly diagnosed cancer in men and is responsible for the fifth highest number of deaths globally. In its early stages, prostate cancer may not exhibit any noticeable symptoms and often progresses slowly, so that it requires active surveillance and detection. Standard biopsy of the prostate that is typically performed using TRUS guidance is one of commonly detection used for prostate cancer. However, several studies showed that MRI-targeted biopsy has better accuracy than standard biopsy. Thus, this meta-analysis aims to evaluate which examination has the ability to detect prostate cancer better between MRI-targeted or standard biopsy.
Methods
Studies were extracted from PubMed databases using several keywords such as ((mri targeted) AND (standard biopsy)) AND (prostate cancer) on May 25th, 2023. Extracted studies were selected through several inclusion criteria, such as randomized controlled trials and cohorts in the last 10 years and exclusion criteria, such as meta-analysis, reviews, case reports and unavailability of full paper access. The quality of the included studies were assessed using Newcastle-Ottawa Scale (NOS) and JADAD scale.
Results
Six total studies were included in these studies, consist of three cohort studies and three RCTs with 4867 mens under suspicion for prostate cancer. Five out of six studies were in good quality, while the other one have fair quality. Meta-analysis showed that MRI-targeted biopsy had a higher detection rate than standard biopsy for prostate cancer with Odds Ratio (M-H, Random Effect Model, 95% CI) 1.72 [0.97, 3.06]. This result proved that MRI-targeted biopsy is superior to standard biopsy for detecting prostate cancer.
Conclusions
In conclusion, detection for prostate cancer is better with MRI-targeted biopsy than standard biopsy due to higher detection rate in MRI-targeted biopsy. However, further studies were required to confirm these findings.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
561P - Mechanisms of osimertinib resistance using circulating tumor DNA analyses for EGFR-mutated non-small cell lung cancer, results from ELUCIDATOR: A prospective observational multicenter study
Presenter: Daijiro Harada
Session: Poster Display
Resources:
Abstract
562P - First-line (1L) osimertinib (osi) ± platinum-pemetrexed in patients (pts) with EGFRm advanced NSCLC: FLAURA2 China cohort
Presenter: Yan Yu
Session: Poster Display
Resources:
Abstract
563P - Real-world effectiveness and safety of first-line osimertinib for EGFR-mutated advanced NSCLC in China (FLOURISH study)
Presenter: Jianya Zhou
Session: Poster Display
Resources:
Abstract
564P - Co-occurring EGFR p.E709X mutation affects the treatment response to the third-generation EGFR-TKIs in EGFR p.G719X-mutant patients with advanced NSCLC
Presenter: Wen Feng Fang
Session: Poster Display
Resources:
Abstract
565P - Genome-guided targeted therapy combination improves survival in patients with advanced EGFR mutation positive NSCLC failing osimertinib
Presenter: Molly Li
Session: Poster Display
Resources:
Abstract
566P - Safety of tepotinib + osimertinib in EGFR-mutant NSCLC with MET amplification after first-line osimertinib
Presenter: Chong Kin Liam
Session: Poster Display
Resources:
Abstract
567P - Furmonertinib in combination with bevacizumab and intrathecal chemotherapy as later-line re-challenge treatment in EGFR –mutated NSCLC patients with leptomeningeal metastasis after third-generation EGFR-TKIs treatment failure
Presenter: Fang Cun
Session: Poster Display
Resources:
Abstract
568P - First-line (1L) osimertinib + platinum-pemetrexed in EGFR-mutated (EGFRm) advanced NSCLC: Updated FLAURA2 safety run-in (SRI) results
Presenter: David Planchard
Session: Poster Display
Resources:
Abstract
569P - Whole-transcriptome sequencing of transformed small-cell lung cancer from EGFR-mutated lung adenocarcinoma reveals LUAD–like and SCLC–like subsets
Presenter: Chan-Yuan Zhang
Session: Poster Display
Resources:
Abstract
570P - First-line osimertinib for patients with advanced NSCLC harboring EGFR mutations: A real-world study
Presenter: Wenxiang Ji
Session: Poster Display
Resources:
Abstract