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
397P - Comparison between Y-site co-infusion versus standard dexamethasone for preventing hypersensitivity reactions from oxaliplatin administration: A randomized controlled trial
Presenter: jarearnjit Phavirunsiri
Session: Poster Display
Resources:
Abstract
398P - Evaluation of the effectiveness of denosumab therapy giant cell tumor of the pelvis
Presenter: Abbos Nurjabov
Session: Poster Display
Resources:
Abstract
399P - Long-term outcomes of patients with gastric cancer who received the best supportive care without any anticancer treatment
Presenter: Yohei Arihara
Session: Poster Display
Resources:
Abstract
401TiP - Oral opioid vs intravenous patient-controlled analgesia (PCA) with hydromorphone bolus-only or continuous infusion to maintain analgesia for severe cancer pain: A randomized phase III trial
Presenter: Cheng Huang
Session: Poster Display
Resources:
Abstract
407P - K-TrackTM: A streamlined personalized assay to detect molecular residual disease in solid tumors
Presenter: Nam Vo
Session: Poster Display
Resources:
Abstract
408P - Increased EGFR and MET expression and corresponding tumor microenvironment (TME) change in hepatocellular carcinoma (HCC) tissues after sorafenib (Sora) treatment
Presenter: Chia Jui Yen
Session: Poster Display
Resources:
Abstract
410P - Systematic evaluation of cell-free DNA fragmentation patterns for cancer diagnosis and enhanced cancer detection through integration of multiple fragmentations
Presenter: Xiangy-Yu Meng
Session: Poster Display
Resources:
Abstract
412P - Multiplex digital spatial profiling (DSP) of protein reveals distinct immune and molecular phenotypes in hepatocellular carcinoma
Presenter: Chia Jui Yen
Session: Poster Display
Resources:
Abstract
413P - Clinical utility of advanced features provided by circulating tumor DNA-based comprehensive genomic profiling
Presenter: Young-gon Kim
Session: Poster Display
Resources:
Abstract
414P - Landscape of ERBB2 mutations in advanced cancers (AC) using circulating tumor DNA (ctDNA) next-generation sequencing (NGS) in Asia and Middle East (AME)
Presenter: Byoung Chul Cho
Session: Poster Display
Resources:
Abstract