Bokhorst LP - Search Results

1

Re: High-dose Radiotherapy and Risk-adapted Androgen Deprivation in Localised Prostate Cancer (DART 01/05): 10-Year Results of a Phase 3 Randomised, Controlled Trial.

Bokhorst LP, Heesterman BL. Bokhorst LP, et al. Eur Urol. 2022 Oct;82(4):441. doi: 10.1016/j.eururo.2022.07.004. Epub 2022 Jul 25. Eur Urol. 2022. PMID: 35902289 Clinical Trial. No abstract available.

2

Prostate-specific antigen-based prostate cancer screening: reduction of prostate cancer mortality after correction for nonattendance and contamination in the Rotterdam section of the European Randomized Study of Screening for Prostate Cancer.

Bokhorst LP, Bangma CH, van Leenders GJ, Lous JJ, Moss SM, Schröder FH, Roobol MJ. Bokhorst LP, et al. Eur Urol. 2014 Feb;65(2):329-36. doi: 10.1016/j.eururo.2013.08.005. Epub 2013 Aug 11. Eur Urol. 2014. PMID: 23954085 Clinical Trial.

3

Differences in Treatment and Outcome After Treatment with Curative Intent in the Screening and Control Arms of the ERSPC Rotterdam.

Bokhorst LP, Kranse R, Venderbos LD, Salman JW, van Leenders GJ, Schröder FH, Bangma CH, Roobol MJ; ERSPC Rotterdam Study Group. Bokhorst LP, et al. Eur Urol. 2015 Aug;68(2):179-82. doi: 10.1016/j.eururo.2014.10.008. Epub 2014 Oct 18. Eur Urol. 2015. PMID: 25457496 Clinical Trial.

4

Magnetic resonance imaging in active surveillance of prostate cancer: a systematic review.

Schoots IG, Petrides N, Giganti F, Bokhorst LP, Rannikko A, Klotz L, Villers A, Hugosson J, Moore CM. Schoots IG, et al. Among authors: bokhorst lp. Eur Urol. 2015 Apr;67(4):627-36. doi: 10.1016/j.eururo.2014.10.050. Epub 2014 Nov 15. Eur Urol. 2015. PMID: 25511988 Review.

5

Do Treatment Differences between Arms Affect the Main Outcome of ERSPC Rotterdam?

Bokhorst LP, Venderbos LD, Schröder FH, Bangma CH, Steyerberg EW, Roobol MJ. Bokhorst LP, et al. J Urol. 2015 Aug;194(2):336-42. doi: 10.1016/j.juro.2015.02.045. Epub 2015 Feb 16. J Urol. 2015. PMID: 25698407 Clinical Trial.

6

Compliance Rates with the Prostate Cancer Research International Active Surveillance (PRIAS) Protocol and Disease Reclassification in Noncompliers.

Bokhorst LP, Alberts AR, Rannikko A, Valdagni R, Pickles T, Kakehi Y, Bangma CH, Roobol MJ; PRIAS study group. Bokhorst LP, et al. Eur Urol. 2015 Nov;68(5):814-21. doi: 10.1016/j.eururo.2015.06.012. Epub 2015 Jun 29. Eur Urol. 2015. PMID: 26138043

7

Risk-based Patient Selection for Magnetic Resonance Imaging-targeted Prostate Biopsy after Negative Transrectal Ultrasound-guided Random Biopsy Avoids Unnecessary Magnetic Resonance Imaging Scans.

Alberts AR, Schoots IG, Bokhorst LP, van Leenders GJ, Bangma CH, Roobol MJ. Alberts AR, et al. Among authors: bokhorst lp. Eur Urol. 2016 Jun;69(6):1129-34. doi: 10.1016/j.eururo.2015.11.018. Epub 2015 Dec 2. Eur Urol. 2016. PMID: 26651990

8

A Decade of Active Surveillance in the PRIAS Study: An Update and Evaluation of the Criteria Used to Recommend a Switch to Active Treatment.

Bokhorst LP, Valdagni R, Rannikko A, Kakehi Y, Pickles T, Bangma CH, Roobol MJ; PRIAS study group. Bokhorst LP, et al. Eur Urol. 2016 Dec;70(6):954-960. doi: 10.1016/j.eururo.2016.06.007. Epub 2016 Jun 19. Eur Urol. 2016. PMID: 27329565

9

Value of Serial Multiparametric Magnetic Resonance Imaging and Magnetic Resonance Imaging-guided Biopsies in Men with Low-risk Prostate Cancer on Active Surveillance After 1 Yr Follow-up.

Hamoen EHJ, Hoeks CMA, Somford DM, van Oort IM, Vergunst H, Oddens JR, Smits GA, Bokhorst LP, Witjes JA, Rovers MM, Hulsbergen-van de Kaa CA, Barentsz JO. Hamoen EHJ, et al. Among authors: bokhorst lp. Eur Urol Focus. 2019 May;5(3):407-415. doi: 10.1016/j.euf.2017.12.008. Epub 2018 Jan 10. Eur Urol Focus. 2019. PMID: 29331622

10

Positive predictive value of prostate biopsy indicated by prostate-specific-antigen-based prostate cancer screening: trends over time in a European randomized trial*.

Bokhorst LP, Zhu X, Bul M, Bangma CH, Schröder FH, Roobol MJ. Bokhorst LP, et al. BJU Int. 2012 Dec;110(11):1654-60. doi: 10.1111/j.1464-410X.2012.11481.x. Epub 2012 Oct 8. BJU Int. 2012. PMID: 23043563 Clinical Trial.

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