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Conference Paper: Multi-parametric magnetic resonance imaging/ultrasound fusion-guided prostate biopsy significantly improves cancer detection in the Chinese population
Title | Multi-parametric magnetic resonance imaging/ultrasound fusion-guided prostate biopsy significantly improves cancer detection in the Chinese population |
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Authors | |
Issue Date | 2017 |
Publisher | Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/IJU |
Citation | 15th Urological Association of Asia (UAA) Congress: Piecing Together Asian Perspectives in Urology, Hong Kong, 4–6 August 2017. In International Journal of Urology, 2017, v. 24 n. Suppl. 1, p. 42 How to Cite? |
Abstract | Introduction and objectives: Conventional transrectal ultrasound(TRUS)-guided 12-core systematic biopsy (SB) of the prostate is ablind procedure with problems of missing clinically significant cancers and over-detection of indolent prostate cancers. Multi-parametric Magnetic Resonance Imaging (mpMRI)/Ultrasound (US) fusion-guidedbiopsy is a new technology to improve the diagnostic accuracy, butAsian results are lacking. The objective of the current study is tocompare the diagnostic efficacy and complication outcome of MRI/USfusion-guided biopsy with conventional TRUS-guided SB of the prostate in a Chinese cohort.
Materials and methods: From July 2015 to December 2016, men with elevated serum prostate-specific antigen (PSA) of 4–20 ng/mLwere counselled for mpMRI of the prostate to detect any lesionsaccording to the Prostate Imaging – Reporting and Data System (PI-RADS) (Version 2). Those with PI-RADS 2–5 lesions underwenttargeted biopsy (TB) plus 12-core SB using the ArtemisâMRI/USfusion platform system. The biopsy outcomes where compared with amatched cohort of 250 patients who underwent conventional TRUS-guided SB in the same period. Complication rates including sepsis,retention of urine and haematuria after the procedure were compared.
Results: A total of 147 patients had pre-biopsy MRI performed, with an average of 1.7⊥0.9 MRI lesions/patient were detected in 132 patients.15 patients with negative MRI had no cancer detected on SB. 30 patientswith PI-RADS 2 lesion(s) only on MRI also had no cancer detected in bothTB and SB. In 102 patients having lesions of intermediate to highsuspicion (PI-RADS 3–5), the overall cancer detection rate by fusionbiopsy (TB+SB) was significantly higher than the conventional SB group(37.3 vs 17.6%, P < 0.0001). TB alone detected more clinicallysignificant cancers (19.6% vs 10.4%, P = 0.02) and yielded significantlylonger mean cancer core length (6.8 ⊥ 5.6 mm vs 3.6 ⊥ 3.1 mm,P = 0.004). TB alone would have avoided diagnosis of 71.4% (10/14) ofthe clinically insignificant cancers at the expense of missing 16.7% (4/24) of the clinically significant cancers. The overall complication rate waslower in the fusion biopsy group (9% vs 20.4%, P = 0.004). While sepsisrate (0.8% vs 3.2%, P = 0.13) and retention of urine (4.5% vs 1.6%,P = 0.09) were similar in the two groups, haematuria was less frequent(3.8% vs 14%, P = 0.002) in the fusion biopsy group.
Conclusion: Multiparametric MRI/US fusion prostate biopsysignificantly improves the cancer detection rate of clinically significant prostate cancer in the Chinese population. It is a promising and safe new modality in prostate cancer diagnosis. |
Description | poster presentation - abstract no. PM05.23 |
Persistent Identifier | http://hdl.handle.net/10722/254837 |
ISSN | 2023 Impact Factor: 1.8 2023 SCImago Journal Rankings: 0.663 |
DC Field | Value | Language |
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dc.contributor.author | Ma, WK | - |
dc.contributor.author | Ho, SHB | - |
dc.contributor.author | Wong, CKW | - |
dc.contributor.author | Lai, ASH | - |
dc.contributor.author | Lam, AKC | - |
dc.contributor.author | Lam, ACS | - |
dc.contributor.author | Yip, LKC | - |
dc.contributor.author | Lai, TCT | - |
dc.contributor.author | Tsang, CF | - |
dc.contributor.author | Ng, ATL | - |
dc.contributor.author | Tsu, HLJ | - |
dc.contributor.author | Yiu, MK | - |
dc.date.accessioned | 2018-06-21T01:07:22Z | - |
dc.date.available | 2018-06-21T01:07:22Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | 15th Urological Association of Asia (UAA) Congress: Piecing Together Asian Perspectives in Urology, Hong Kong, 4–6 August 2017. In International Journal of Urology, 2017, v. 24 n. Suppl. 1, p. 42 | - |
dc.identifier.issn | 0919-8172 | - |
dc.identifier.uri | http://hdl.handle.net/10722/254837 | - |
dc.description | poster presentation - abstract no. PM05.23 | - |
dc.description.abstract | Introduction and objectives: Conventional transrectal ultrasound(TRUS)-guided 12-core systematic biopsy (SB) of the prostate is ablind procedure with problems of missing clinically significant cancers and over-detection of indolent prostate cancers. Multi-parametric Magnetic Resonance Imaging (mpMRI)/Ultrasound (US) fusion-guidedbiopsy is a new technology to improve the diagnostic accuracy, butAsian results are lacking. The objective of the current study is tocompare the diagnostic efficacy and complication outcome of MRI/USfusion-guided biopsy with conventional TRUS-guided SB of the prostate in a Chinese cohort. Materials and methods: From July 2015 to December 2016, men with elevated serum prostate-specific antigen (PSA) of 4–20 ng/mLwere counselled for mpMRI of the prostate to detect any lesionsaccording to the Prostate Imaging – Reporting and Data System (PI-RADS) (Version 2). Those with PI-RADS 2–5 lesions underwenttargeted biopsy (TB) plus 12-core SB using the ArtemisâMRI/USfusion platform system. The biopsy outcomes where compared with amatched cohort of 250 patients who underwent conventional TRUS-guided SB in the same period. Complication rates including sepsis,retention of urine and haematuria after the procedure were compared. Results: A total of 147 patients had pre-biopsy MRI performed, with an average of 1.7⊥0.9 MRI lesions/patient were detected in 132 patients.15 patients with negative MRI had no cancer detected on SB. 30 patientswith PI-RADS 2 lesion(s) only on MRI also had no cancer detected in bothTB and SB. In 102 patients having lesions of intermediate to highsuspicion (PI-RADS 3–5), the overall cancer detection rate by fusionbiopsy (TB+SB) was significantly higher than the conventional SB group(37.3 vs 17.6%, P < 0.0001). TB alone detected more clinicallysignificant cancers (19.6% vs 10.4%, P = 0.02) and yielded significantlylonger mean cancer core length (6.8 ⊥ 5.6 mm vs 3.6 ⊥ 3.1 mm,P = 0.004). TB alone would have avoided diagnosis of 71.4% (10/14) ofthe clinically insignificant cancers at the expense of missing 16.7% (4/24) of the clinically significant cancers. The overall complication rate waslower in the fusion biopsy group (9% vs 20.4%, P = 0.004). While sepsisrate (0.8% vs 3.2%, P = 0.13) and retention of urine (4.5% vs 1.6%,P = 0.09) were similar in the two groups, haematuria was less frequent(3.8% vs 14%, P = 0.002) in the fusion biopsy group. Conclusion: Multiparametric MRI/US fusion prostate biopsysignificantly improves the cancer detection rate of clinically significant prostate cancer in the Chinese population. It is a promising and safe new modality in prostate cancer diagnosis. | - |
dc.language | eng | - |
dc.publisher | Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/IJU | - |
dc.relation.ispartof | International Journal of Urology | - |
dc.relation.ispartof | The 15th Urological Association of Asia Congress | - |
dc.rights | The definitive version is available at www.blackwell-synergy.com | - |
dc.title | Multi-parametric magnetic resonance imaging/ultrasound fusion-guided prostate biopsy significantly improves cancer detection in the Chinese population | - |
dc.type | Conference_Paper | - |
dc.identifier.email | Ma, WK: mwk054@hku.hk | - |
dc.identifier.email | Ho, SHB: hobrian@hku.hk | - |
dc.identifier.email | Wong, CKW: kwwongab@hku.hk | - |
dc.identifier.email | Ng, ATL: ada5022@hku.hk | - |
dc.identifier.email | Tsu, HLJ: jamestsu@hku.hk | - |
dc.identifier.email | Yiu, MK: pmkyiu@hku.hk | - |
dc.identifier.hkuros | 285485 | - |
dc.identifier.volume | 24 | - |
dc.identifier.issue | Suppl. 1 | - |
dc.identifier.spage | 42 | - |
dc.identifier.epage | 42 | - |
dc.publisher.place | Australia | - |
dc.identifier.issnl | 0919-8172 | - |