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Dive into the research topics where Francis Ting is active.

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Featured researches published by Francis Ting.


BJUI | 2016

68Ga-PSMA has a high detection rate of prostate cancer recurrence outside the prostatic fossa in patients being considered for salvage radiation treatment

Pim J. van Leeuwen; George Hruby; Andrew Kneebone; Francis Ting; Ben Thompson; Quoc Nguyen; Bao Ho; Louise Emmett

To examine the detection rates of 68Ga‐PSMA‐positron emission tomography (PET)/computed tomography (CT) in patients with biochemical recurrence (BCR) after radical prostatectomy (RP), and also the impact on their management.


BJUI | 2017

Prospective evaluation of 68Gallium-prostate-specific membrane antigen positron emission tomography/computed tomography for preoperative lymph node staging in prostate cancer

Pim J. van Leeuwen; Louise Emmett; Bao Ho; Warick Delprado; Francis Ting; Quoc Nguyen

To assess the accuracy of 68Gallium‐prostate‐specific membrane antigen (68Ga‐PSMA) positron emission tomography/computed tomography (PET/CT) for lymph node (LN) staging in intermediate‐ and high‐risk prostate cancer (PCa).


Prostate Cancer and Prostatic Diseases | 2016

Focal irreversible electroporation for prostate cancer: functional outcomes and short-term oncological control.

Francis Ting; Minh Tran; Maret Böhm; Amila Siriwardana; P.J. van Leeuwen; A-M Haynes; Warick Delprado; Ron Shnier

Background:Current data on the use of irreversible electroporation (IRE) in the treatment of prostate cancer (PCa) is limited. We aim to evaluate the safety, short-term functional and oncological outcomes of focal IRE in low-intermediate risk PCa.Methods:Between February 2013 and May 2014, 32 consecutive men underwent IRE at a single centre. Patients with low-intermediate risk PCa who had not received previous PCa treatment were included for analysis. The tumour was ablated using 3–6 electrodes, ensuring a minimum 5-mm safety margin around the visible magnetic resonance imaging (MRI) lesion. Follow-up included recording Clavien complications, Expanded Prostate Cancer Index Composite (EPIC) questionnaires (baseline, 1.5, 3, 6 months), 6-month multi-parametric MRI (mp-MRI) and 7-month biopsy. Findings on mp-MRI and biopsy were sub-divided into infield, adjacent or outfield of the treatment zone.Results:Twenty-five men were included for final analysis. Safety follow-up revealed one Clavien Grade 3 complication and five Grade 1 complications. Functional follow-up confirmed no significant change in American Urological Association urinary symptom score, sexual or bowel function. Infield, there were no suspicious findings on mp-MRI (n=24) or biopsy (n=21) in all patients. Adjacent to the treatment zone, five (21%) had suspicious findings on mp-MRI with four (19%) proving to be significant on biopsy. Outfield, there were two (8%) with suspicious findings on mp-MRI and one (5%) significant finding on biopsy. For the five patients with significant findings on follow-up biopsy, one is awaiting repeat IRE, one had radical prostatectomy and three remained on active surveillance.Conclusions:In selected patients with low-intermediate risk PCa, focal IRE appears to be safe with minimal morbidity. There were no infield recurrences and 76% of patients were histologically free of significant cancer at 8 months. Almost all recurrences were adjacent to the treatment zone, and this was addressed by widening the treatment margins.


BJUI | 2017

A multiparametric magnetic resonance imaging-based risk model to determine the risk of significant prostate cancer prior to biopsy

Pim J. van Leeuwen; Andrew Hayen; James Thompson; Daniel Moses; Ron Shnier; Maret Böhm; Magdaline Abuodha; Anne-Maree Haynes; Francis Ting; Jelle O. Barentsz; Monique J. Roobol; Justin Vass; K. Rasiah; Warick Delprado

To develop and externally validate a predictive model for detection of significant prostate cancer.


The Prostate | 2015

Tumor volume in insignificant prostate cancer: Increasing the threshold is a safe approach to reduce over-treatment

Francis Ting; Pim J. van Leeuwen; Warick Delprado; Anne-Maree Haynes; Phillip Brenner

There are conflicting results in the literature regarding the tumor volume (TV) threshold that defines insignificant prostate cancer (PCa). In this study, we retrospectively evaluate the association of an increasing TV with biochemical recurrence (BCR) following radical prostatectomy (RP) in order to provide further clarification surrounding the TV threshold definition for insignificant PCa.


BJUI | 2018

Focal irreversible electroporation as primary treatment for localized prostate cancer

Willemien van den Bos; Matthijs J. Scheltema; Amila Siriwardana; Anton M.F. Kalsbeek; James Thompson; Francis Ting; Maret Böhm; Anne-Maree Haynes; Ron Shnier; Warick Delprado

To determine the safety, quality of life (QoL) and short‐term oncological outcomes of primary focal irreversible electroporation (IRE) for the treatment of localized prostate cancer (PCa), and to identify potential risk factors for oncological failure.


Prostate Cancer | 2016

Assessment of the Performance of Magnetic Resonance Imaging/Ultrasound Fusion Guided Prostate Biopsy against a Combined Targeted Plus Systematic Biopsy Approach Using 24-Core Transperineal Template Saturation Mapping Prostate Biopsy

Francis Ting; Pim J. van Leeuwen; James Thompson; Ron Shnier; Daniel Moses; Warick Delprado

Objective. To compare the performance of multiparametric resonance imaging/ultrasound fusion targeted biopsy (MRI/US-TBx) to a combined biopsy strategy (MRI/US-TBx plus 24-core transperineal template saturation mapping biopsy (TTMB)). Methods. Between May 2012 and October 2015, all patients undergoing MRI/US-TBx at our institution were included for analysis. Patients underwent MRI/US-TBx of suspicious lesions detected on multiparametric MRI +/− simultaneous TTMB. Subgroup analysis was performed on patients undergoing simultaneous MRI/US-TBx + TTMB. Primary outcome was PCa detection. Significant PCa was defined as ≥Gleason score (GS) 3 + 4 = 7 PCa. McNemars test was used to compare detection rates between MRI/US-TBx and the combined biopsy strategy. Results. 148 patients underwent MRI/US-TBx and 80 patients underwent MRI/US-TBx + TTMB. In the MRI/US-TBx versus combined biopsy strategy subgroup analysis (n = 80), there were 55 PCa and 38 significant PCa. The detection rate for the combined biopsy strategy versus MRI/US-TBx for significant PCa was 49% versus 40% (p = 0.02) and for insignificant PCa was 20% versus 10% (p = 0.04), respectively. Eleven cases (14%) of significant PCa were detected exclusively on MRI/US-TBx and 7 cases (8.7%) of significant PCa were detected exclusively on TTMB. Conclusions. A combined biopsy approach (MRI/US-TBx + TTMB) detects more significant PCa than MRI/US-TBx alone; however, it will double the detection rate of insignificant PCa.


BJUI | 2017

Feasibility and safety of focal irreversible electroporation as salvage treatment for localized radio-recurrent prostate cancer

Matthijs J. Scheltema; Willemien van den Bos; Amila Siriwardana; Anton M.F. Kalsbeek; James Thompson; Francis Ting; Maret Böhm; Anne-Maree Haynes; Ron Shnier; Warick Delprado

To evaluate the feasibility, safety, early quality‐of‐life (QoL) and oncological outcomes of salvage focal irreversible electroporation (IRE) for radio‐recurrent prostate cancer (PCa).


Journal of Vascular and Interventional Radiology | 2016

Step-by-Step Technique for Irreversible Electroporation of Focal Prostate Cancer: An Instructional Video Guide

Francis Ting; Pim J. van Leeuwen

Focal therapy has emerged as a tissue-sparing treatment modality for selected men with low to intermediate volume, localized prostate cancer with the advantage of reducing treatment morbidity because of preservation of untreated prostate tissue and surrounding structures. Irreversible electroporation is an emerging interventional focal therapy modality that uses high voltage electrical fields to induce cell death. This instructional video guide (Fig) serves as an easy-to-understand, comprehensive educational tool so that a broader audience can gain an understanding of the techniques involved in this treatment modality.


Prostate Cancer | 2016

Predicting Low-Risk Prostate Cancer from Transperineal Saturation Biopsies.

Pim J. van Leeuwen; Amila Siriwardana; Monique J. Roobol; Francis Ting; Daan Nieboer; James Thompson; Warick Delprado; A.M. Haynes; Phillip Brenner

Introduction. To assess the performance of five previously described clinicopathological definitions of low-risk prostate cancer (PC). Materials and Methods. Men who underwent radical prostatectomy (RP) for clinical stage ≤T2, PSA <10 ng/mL, Gleason score <8 PC, diagnosed by transperineal template-guided saturation biopsy were included. The performance of five previously described criteria (i.e., criteria 1–5, criterion 1 stringent (Gleason score 6 + ≤5 mm total max core length PC + ≤3 mm max per core length PC) up to criterion 5 less stringent (Gleason score 6-7 with ≤5% Gleason grade 4) was analysed to assess ability of each to predict insignificant disease in RP specimens (defined as Gleason score ≤6 and total tumour volume <2.5 mL, or Gleason score 7 with ≤5% grade 4 and total tumour volume <0.7 mL). Results. 994 men who underwent RP were included. Criterion 4 (Gleason score 6) performed best with area under the curve of receiver operating characteristics 0.792. At decision curve analysis, criterion 4 was deemed clinically the best performing transperineal saturation biopsy-based definition for low-risk PC. Conclusions. Gleason score 6 disease demonstrated a superior trade-off between sensitivity and specificity for clarifying low-risk PC that can guide treatment and be used as reference test in diagnostic studies.

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Dive into the Francis Ting's collaboration.

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Pim J. van Leeuwen

Erasmus University Rotterdam

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Amila Siriwardana

Garvan Institute of Medical Research

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Anne-Maree Haynes

Garvan Institute of Medical Research

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Phillip Brenner

St. Vincent's Health System

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Maret Böhm

Garvan Institute of Medical Research

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James Thompson

Garvan Institute of Medical Research

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Monique J. Roobol

Erasmus University Medical Center

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Carlo Yuen

St. Vincent's Health System

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