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Your search keyword '"Van Der Voort Van Zyp, Jochem R.N."' showing total 38 results
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2. Magnetic Resonance-Guided Adaptive Radiation Therapy for Prostate Cancer: The First Results from the MOMENTUM study—An International Registry for the Evidence-Based Introduction of Magnetic Resonance-Guided Adaptive Radiation Therapy

Author

Teunissen, Frederik R., Willigenburg, Thomas, Tree, Alison C., Hall, William A., Choi, Seungtaek L., Choudhury, Ananya, Christodouleas, John P., de Boer, Johannes C.J., de Groot-van Breugel, Eline N., Kerkmeijer, Linda G.W., Pos, Floris J., Schytte, Tine, Vesprini, Danny, Verkooijen, Helena M., and van der Voort van Zyp, Jochem R.N.

Published
2023
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20. Bringing online adaptive radiotherapy to a standard C-arm linac

Author

Groot Koerkamp, Maureen L., Bol, Gijsbert H., Kroon, Petra S., Krikke, Lean L., Harderwijk, Tessa, Zoetelief, Annelies J., Scheeren, Annick, van der Vegt, Stefan, Plat, Annika, Hes, Jochem, van Gasteren, Ineke B.A., Renders, Esmee R.T., Rutgers, Reijer H.A., Kok, Saskia W., van Kaam, Joost, Schimmel-de Kogel, Geja J., Sikkes, Gonda G., Winkel, Dennis, van Rijssel, Michael J., Wopereis, André J.M., Ishakoglu, Kübra, Noteboom, Juus L., van der Voort van Zyp, Jochem R.N., Beck, Naomi, Soeterik, Timo F.W., van de Pol, Sandrine M.G., Eppinga, Wietse S.C., van Es, Corine A., and Raaymakers, Bas W.

Published
2024
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22. Multivariable model development and internal validation for prostate cancer specific survival and overall survival after whole-gland salvage Iodine-125 prostate brachytherapy

Author

Peters, Max, van der Voort van Zyp, Jochem R.N., Moerland, Marinus A., Hoekstra, Carel J., van de Pol, Sandrine, Westendorp, Hendrik, Maenhout, Metha, Kattevilder, Rob, Verkooijen, Helena M., van Rossum, Peter S.N., Ahmed, Hashim U., Shah, Taimur T., Emberton, Mark, and van Vulpen, Marco

Published
2016
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25. Prostate tumor delineation using multiparametric magnetic resonance imaging: Inter-observer variability and pathology validation

Author

Steenbergen, Peter, Haustermans, Karin, Lerut, Evelyne, Oyen, Raymond, De Wever, Liesbeth, Van den Bergh, Laura, Kerkmeijer, Linda G.W., Pameijer, Frank A., Veldhuis, Wouter B., van der Voort van Zyp, Jochem R.N., Pos, Floris J., Heijmink, Stijn W., Kalisvaart, Robin, Teertstra, Hendrik J., Dinh, Cuong V., Ghobadi, Ghazaleh, and van der Heide, Uulke A.

Published
2015
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26. In response to Grivas et al

Author

van den Berg, Ingeborg, Savenije, Mark H.F., Teunissen, Frederik R., van de Pol, Sandrine M.G., Rasing, Marnix J.A., van Melick, Harm H.E., Brink, Wyger M., de Boer, Johannes C.J., van den Berg, Cornelis A.T., and van der Voort van Zyp, Jochem R.N.

Published
2023
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32. Neurovascular-Sparing MR-Guided Adaptive Radiotherapy in Prostate Cancer; Defining the Potential Population for Erectile Function-Sparing Treatment.

Author

Teunissen, Frederik R., van der Voort van Zyp, Jochem R.N., Verkooijen, Helena M., and Wortel, Ruud C.

Subjects
*PROSTATE cancer, *CANCER radiotherapy, *IMPOTENCE, *DATA plans
Abstract

Magnetic resonance-guided adaptive radiotherapy (MRgRT) enables neurovascular-sparing treatment for localized prostate cancer (PCa). The aim of this treatment is preservation of erectile function by sparing the neurovascular bundles, the internal pudendal arteries, the corpora cavernosa, and the penile bulb. Internal pudendal arteries, corpora cavernosa, and penile bulb sparing can generally be achieved in all patients, but NVB sparing can be challenging due to its proximity to the prostate and is therefore dependent on tumor location. PCa patients that have sufficient erectile function at baseline and favorable tumor characteristics might benefit from this treatment. Currently, it is unclear what proportion of patients are eligible for neurovascular-sparing treatment and to what extent this is technically feasible. To define the eligibility and technical feasibility for neurovascular-sparing MRgRT in intermediate-risk localized PCa patients. A consecutive series of men that received 5 × 7.25 gray (Gy) MRgRT for localized PCa were included. Baseline erectile function was assessed using the International Index of Erectile Function (IIEF)-5 questionnaire. Additionally, the ability of sparing the neurovascular bundles was assessed in all patients. Per neurovascular-sparing protocol, the dominant intraprostatic lesion with a 4 mm isotropic margin should receive 34.44 Gy in ≥ 99% of the volume (i.e., high-dose area). When the high-dose area directly borders or overlaps the NVB because of a dorsolateral position of the dominant intraprostatic lesion, sparing of the NVB was considered not feasible on that side. Patient-reported IIEF-5 baseline questionnaires and the technical feasibility of NVB sparing were assessed. Of the 102 men that completed the IIEF-5 questionnaire at baseline, 49.0% of patients reported to have an IIEF-5 score of ≥ 17. In those patients, the NVB could technically have been spared bilaterally in 20.0% and unilaterally in 68.0%. Our findings define the potential population for neurovascular-sparing MRgRT for localized PCa and indicate the proportion in which the NVB can technically be spared. The major strength of this study is the prospective collection of data. The limitations include that the neurovascular-sparing feasibility definition is based on pre-clinical planning data. A substantial group of 49.0% of patients in our study had mild or no erectile dysfunction at baseline. Of these patients, the NVB could technically have been spared bilaterally in 20.0% and unilaterally in 68.0% during MRgRT. Trials need to assess the effect of neurovascular-sparing MRgRT on erectile function. Teunissen FR, van der Voort van Zyp JRN, Verkooijen HM, et al., Neurovascular-Sparing MR-Guided Adaptive Radiotherapy in Prostate Cancer; Defining the Potential Population for Erectile Function-Sparing Treatment. J Sex Med 2022;19:1196–1200. [ABSTRACT FROM AUTHOR]

Published
2022
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34. Patient-Reported Outcomes Following Magnetic Resonance-Guided Radiation Therapy for Prostate Cancer: A Systematic Review and Meta-Analysis.

Author

Westerhoff, Jasmijn M., Lalmahomed, Tariq A., Meijers, Lieke T.C., Henke, Lauren, Teunissen, Frederik R., Bruynzeel, Anna M.E., Alongi, Filippo, Hall, William A., Kishan, Amar U., Intven, Martijn P.W., Verkooijen, Helena M., van der Voort van Zyp, Jochem R.N., and Daamen, Lois A.

Subjects
*PROSTATE cancer patients, *CANCER radiotherapy, *PATIENT reported outcome measures, *QUALITY of life, *RADIOTHERAPY
Abstract

This systematic review provides an overview of literature on the impact of magnetic resonance–guided radiation therapy (MRgRT) on patient-reported outcomes (PROs) in patients with prostate cancer (PC). A systematic search was performed in October 2023 in PubMed, EMBASE, and Cochrane Library. The Patient, Intervention, Comparison, Outcomes, and Study design (PICOS) framework was used to determine eligibility criteria. Included were studies assessing PROs following MRgRT for PC with a sample size >10. Methodological quality was assessed using the Cochrane's Risk of Bias in Nonrandomized Studies - of Interventions and Cochrane's risk of bias tool for randomized trials. Relevant mean differences (MDs) compared with pre-RT were interpreted using minimal important differences. Meta-analyses were performed using random-effects models. Between-study heterogeneity was assessed using the I2 statistic. Eleven observational studies and 1 randomized controlled trial (n = 897) were included. Nine studies included patients with primary PC with MRgRT as first-line treatment (n = 813) and 3 with MRgRT as second-line treatment (n = 84). Substantial risk of bias was found in 5 studies. European Organization for Research and Treatment Quality of Life Questionnaire (EORTC QLQ) core 30 (C30) and EORTC QLQ prostate cancer module (PR25) scores were pooled from 3 studies, and Expanded Prostate Cancer Index Composite (EPIC)-26 scores were pooled from 4 studies. Relevant MDs for the urinary domain were found with the EPIC-26 (MD, −10.0; 95% CI, −12.0 to −8.1; I2 = 0%) and the EORTC QLQ-PR25 (MD, 8.6; 95% CI, −4.7 to 22.0; I2 = 97%), both at end-RT to 1-month follow-up. Relevant MDs for the bowel domain were found with the EPIC-26 (MD, −4.7; 95% CI, −9.2 to −0.2; I2 = 82%) at end-RT or 1-month follow-up, but not with the EORTC QLQ-PR25. For both domains, no relevant MDs were found after 3 months of follow-up. No relevant MDs were found in the general quality of life domains of the EORTC QLQ C30. MRgRT for PC results in a temporary worsening of patient-reported urinary and bowel symptoms during the first month after treatment compared with pre-RT, resolving at 3 months. No clinically relevant changes were found for general quality of life domains. These results provide important information for patient counseling and can serve as a benchmark for future studies. [ABSTRACT FROM AUTHOR]

Published
2024
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35. MRI-Guided Ultrafocal Salvage High-Dose-Rate Brachytherapy for Localized Radiorecurrent Prostate Cancer: Updated Results of 50 Patients.

Author

van Son, Marieke Juliet, Peters, Max, Moerland, Marinus A., Lagendijk, Jan J.W., Eppinga, Wietse S.C., Shah, Taimur T., Ahmed, Hashim U., and van der Voort van Zyp, Jochem R.N.

Subjects
*WASTE salvage, *RADIOISOTOPE brachytherapy, *PROSTATE cancer, *POSITRON emission tomography, *ENDORECTAL ultrasonography, *RELATIVE medical risk, *SAFETY, *RESEARCH, *RESEARCH methodology, *MAGNETIC resonance imaging, *EVALUATION research, *MEDICAL cooperation, *TREATMENT effectiveness, *DISEASE relapse, *COMPARATIVE studies, *RADIATION doses, *QUALITY of life, *RESEARCH funding, *RADIOTHERAPY, *PROSTATE tumors, *TUMOR grading
Abstract

Purpose: Most patients with local prostate cancer recurrence after radiation therapy undergo palliative androgen deprivation therapy because whole-gland salvage treatments have a high risk of severe toxicity. Focal treatment reduces this risk while offering a second opportunity for cure. We report updated outcomes of ultrafocal salvage high-dose-rate brachytherapy (HDR-BT).Methods and Materials: Prospectively collected data from the first 50 treated patients were analyzed. Disease status was assessed by 3T multiparametric magnetic resonance imaging (MRI), 18F-Choline or 68Ga-prostate-specific membrane antigen positron emission tomography/computed tomography, and systematic or tumor-targeted biopsies. Ultrafocal salvage HDR-BT (1 × 19 Gy) was performed by implanting the clinical target volume (CTV: gross tumor volume + 5 mm margin) under fused transrectal ultrasound/MRI guidance. Follow-up included toxicity grading (using Common Terminology Criteria for Adverse Events 4.0), quality of life assessment, and prostate-specific antigen (PSA) testing.Results: Median follow-up was 31 months. Median CTV D95% was 18.8 Gy. We observed 2% grade 3 genitourinary toxicity, no grade 3 gastrointestinal toxicity, and 22% newly developed grade 3 erectile dysfunction. Five of 13 patients (38%) with self-reported pretreatment potency (International Index of Erectile Function >17) remained potent. Clinically relevant quality of life deterioration was reported for only 6 of 31 items and was not statistically significant. Biochemical failure (nadir + 2) occurred in 26 patients. Among intraprostatic recurrences, 73% were in field. After 2.5 years, biochemical disease-free survival was 51% (95% confidence interval, 37%-69%), metastases-free survival was 75% (64%-89%), androgen deprivation therapy-free survival was 90% (82%-99%), and overall survival was 98% (94%-100%). Presalvage PSA, CTV size, and stage ≥T3 were significantly associated with biochemical failure. Higher-risk patients (stage ≥T3, PSA ≥10, or PSA double time ≤9 months) had 25% biochemical disease-free survival at 2.5 years versus 71% for lower-risk patients.Conclusions: At this early stage, MRI-guided ultrafocal HDR-BT seems to be a safe salvage treatment option, with acceptable biochemical control in a well-selected group of patients and potential for effectively postponing androgen deprivation therapy. [ABSTRACT FROM AUTHOR]

Published
2020
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37. In Regard to Genebes et al.

Author

Moerland, Marinus A., Maenhout, Metha, van der Voort van Zyp, Jochem R.N., Noteboom, Juus L., Eppinga, Wietse S.C., van Vulpen, Marco, Monninkhof, Evelyn M., and Verkooijen, Helena M.

Published
2014
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