Petra S. Kroon
Utrecht University
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Featured researches published by Petra S. Kroon.
Acta Oncologica | 2014
Eelco Lens; Astrid van der Horst; Petra S. Kroon; Jeanin E. van Hooft; Raquel Dávila Fajardo; Paul Fockens; Geertjan van Tienhoven; A. Bel
Abstract Background. In radiotherapy, the magnitude of respiratory-induced tumor motion is often measured using a single four-dimensional computed tomography (4DCT). This magnitude is required to determine the internal target volume. The aim of this study was to compare the magnitude of respiratory-induced motion of pancreatic tumors on a single 4DCT with the motion on daily cone beam CT (CBCT) scans during a 3–5-week fractionated radiotherapy scheme. In addition, we investigated changes in the respiratory motion during the treatment course. Material and methods. The mean peak-to-peak motion (i.e. magnitude of motion) of pancreatic tumors was measured for 18 patients using intratumoral gold fiducials visible on CBCT scans made prior to each treatment fraction (10–27 CBCTs per patient; 401 CBCTs in total). For each patient, these magnitudes were compared to the magnitude measured on 4DCT. Possible time trends were investigated by applying linear fits to the tumor motion determined from daily CBCTs as a function of treatment day. Results. We found a significant (p ≤ 0.01) difference between motion magnitude on 4DCT and on CBCT in superior-inferior, anterior-posterior and left-right direction, in 13, 9 and 12 of 18 patients, respectively. In the anterior- posterior and left-right direction no fractions had a difference ≥ 5 mm. In the superior-inferior direction the difference was ≥ 5 mm for 17% of the 401 fractions. In this direction, a significant (p ≤ 0.05) time trend in tumor motion was observed in 4 of 18 patients, but all trends were small (− 0.17–0.10 mm/day) and did not explain the large differences in motion magnitude between 4DCT and CBCT. Conclusion. A single measurement of the respiratory-induced motion magnitude of pancreatic tumors using 4DCT is often not representative for the magnitude during daily treatment over a 3–5-week radiotherapy scheme. For this patient group it may be beneficial to introduce breath-hold to eliminate respiratory-induced tumor motion.
Acta Oncologica | 2015
A. Ramlov; Petra S. Kroon; Ina M. Jürgenliemk-Schulz; Astrid A.C. de Leeuw; Lars Christian Gormsen; L. Fokdal; Kari Tanderup; Jacob Christian Lindegaard
ABSTRACT Background. Despite local control now exceeding 90% with image-guided adaptive brachytherapy (IGABT), regional and distant metastases continue to curb survival in locally advanced cervical cancer. As regional lymph nodes often represent first site of metastatic spread, improved nodal control could improve survival. The aim of this study was to examine optimal volume and dose of external beam radiotherapy (EBRT) to maximize regional control including dose contribution from IGABT. Material and methods. In total 139 patients from the EMBRACE study were analyzed. Individual nodal dose was determined by dose-maps from EBRT and IGABT. All PET/CT scans were re-evaluated and nodal maximal standard uptake value (SUVmax) was determined. Nodal failures were registered to planning scans and related to boosted nodes and treated volume. Relation between SUVmax and nodal control as well as the pattern of regional nodal failure were analyzed. Results. Eighty-four patients were node positive. Nine patients had all metastatic nodes surgically removed. Seventy-five patients had 209 nodes boosted with EBRT. Median nodal boost dose was 62 Gy EQD2 (53–69 Gy EQD2). Median SUVmax was 6 (2–22). No patients had persistent nodal disease, but six patients recurred in a boosted node. SUVmax was significantly higher in nodes that recurred (p = 0.02). However, there was no correlation to nodal dose or volume. Twenty-one patients had a nodal failure including para-aortic nodal (PAN) metastases above the irradiated volume. Nine patients had a PAN-only failure. Patients receiving ≤ 4 cycles of weekly cisplatin had higher risk of nodal failure (p < 0.01). Conclusion. Current RT practice provides a high level of control in both boosted nodes and the elective irradiated regional target. However, a high nodal SUVmax is a negative prognostic predictor for nodal control. Attention should be raised to administration of a complete schedule of concurrent chemotherapy as well as treatment of para-aortic nodes.
Radiotherapy and Oncology | 2017
A. Andreychenko; Petra S. Kroon; Matteo Maspero; Ina M. Jürgenliemk-Schulz; Astrid A.C. de Leeuw; Marnix G. E. H. Lam; Jan J.W. Lagendijk; Cornelis A.T. van den Berg
PURPOSE For patients with cervical cancer the delivery of chemotherapy with radiotherapy improves survival compared with radiotherapy alone. However, high rates of acute hematologic toxicity occur when combining both therapies due to the damage of the red bone marrow (RBM). This study aimed to reduce the radiation damage to the RBM. A tool has been developed for semi-automatic delineation of the red bone marrow based on MR-only. This delineation can be included into the treatment planning process to reduce the volume of RBM irradiated in patients receiving pelvic radiation therapy. METHODS 13 patients with cervical cancer were enrolled. All the patients underwent MR, CT and FDG-PET imaging. A tool for RBM determination from water and fat MR images was developed. Our MR-based RBM tool was optimized and validated with the FDG-PET scans of the patients. RESULTS Our tool identified RBM regions in the pelvic area. The mean total volume of these regions was 34% of the pelvic bone marrow. The corresponding SUV values based on the FDG-PET scans were above the reported threshold of active/red bone marrow. CONCLUSION This study shows that delineations of the RBM for the radiotherapy with RBM sparing can be generated semi-automatically using MR scans only.
Cureus | 2018
Dennis Winkel; G.H. Bol; Ilse H Kiekebosch; Bram van Asselen; Petra S. Kroon; Ina M. Jürgenliemk-Schulz; B W Raaymakers
The superior soft tissue contrast provided by magnetic resonance (MR) images on the 1.5T MR-linac allows for the incorporation of patient anatomy information. In this retrospective case study, we present the simulated dosimetric effects and timings of full online replanning as compared to the five plan adaptation methods currently available on the 1.5T MR-linac treatment system. For this case, it is possible to create treatment plans with all six methods within a time slot suitable for an online treatment procedure. However, large dosimetric differences between the plan adaptation methods and full online replanning are present with regards to target coverage and dose to organs at risk (OARs).
Radiotherapy and Oncology | 2015
C. Nomden; A. de Leeuw; E.M. Monninkhof; M. Schippers; Kari Tanderup; Petra S. Kroon; A. Ramlov; J.C. Lindegaard; Richard Pötter; Christine Haie-Meder; Peter Hoskin; Barbara Segedin; I.M. Jürgenliemk-Schulz
Nodal failure after (chemo-)radiation and MRI guided adaptive BT in cervical cancer: a sub-analysis within EMBRACE C.N. Nomden, A.A.C. De Leeuw, E.M. Monninkhof, M. Schippers, K. Tanderup, P.S. Kroon, A. Ramlov, J.C. Lindegaard, R. Pötter, C. Haie-Meder, P. Hoskin, B. Segedin, I.M. Jürgenliemk-Schulz UMC Utrecht, Radiation Oncology, Utrecht, The Netherlands UMC Utrecht, Julius Center for Health Sciences and Primary Care, Utrecht, The Netherlands Aarhus University Hospital, Oncology, Aarhus, Denmark Comprehensive Cancer Center Medical University of Vienna, Oncology, Vienna, Austria Gustave Roussy, Radiation Oncology, Villejuif, France Mount Vernon Hospital, Cancer centre, Northwood, United Kingdom Institute of Oncology, Radiotherapy, Ljubljana, Slovenia
Radiotherapy and Oncology | 2018
I.H. Kiekebosch; D. Winkel; A.M. Werensteijn-Honingh; J. Hes; M. Intven; W.S.C. Eppinga; G.H. Bol; B W Raaymakers; I.M. Jürgenliemk-Schulz; Petra S. Kroon
Radiotherapy and Oncology | 2018
D. Winkel; G.H. Bol; A.M. Werensteijn-Honingh; I.H. Kiekebosch; J. Hes; M. Intven; W.S.C. Eppinga; B W Raaymakers; I.M. Jürgenliemk-Schulz; Petra S. Kroon
Acta Oncologica | 2018
Dennis Winkel; Petra S. Kroon; Anita M. Werensteijn-Honingh; G.H. Bol; B W Raaymakers; Ina M. Jürgenliemk-Schulz
Radiotherapy and Oncology | 2017
D. Winkel; Petra S. Kroon; J. Hes; G.H. Bol; B W Raaymakers; I.M. Jürgenliemk-Schulz
Radiotherapy and Oncology | 2015
A. Ramlov; Petra S. Kroon; I. Jürgenliemk_Schulz; A. de Leeuw; L. Fokdal; Kari Tanderup; J.C. Lindegaard