Skip to main content

Intrafractional stability of MR-guided online adaptive SBRT for prostate cancer



MR-guided online adaptive stereotactic body radiation therapy (SBRT) for prostate cancer aims to reduce toxicity by full compensation of interfractional uncertainties. However, the process of online adaptation currently takes approximately 45 min during which intrafractional movements remain unaccounted for. This study aims to analyze the dosimetric benefit of online adaptation and to evaluate its robustness over the duration of one treatment fraction.


Baseline MR-scans at a MR-linear accelerator were acquired for ten healthy male volunteers for generation of mock-prostate SBRT plans with a dose prescription of 5 × 7.25 Gy. On a separate day, online MR-guided adaptation (ViewRay® MRIdian) was performed, and thereafter MR images were acquired every 15 min for 1 h to assess the stability of the adapted plan.


A dosimetric benefit of online MR-guided adaptive re-planning was observed in 90% of volunteers. The median D95CTV- and D95PTV-coverage was improved from 34.8 to 35.5 Gy and from 30.7 to 34.6 Gy, respectively. Improved target coverage was not associated with higher dose to the organs at risk, most importantly the rectum (median D1ccrectum baseline plan vs. adapted plan 33.3 Gy vs. 32.3 Gy). The benefit of online adaptation remained stable over 45 min for all volunteers. However, at 60 min, CTV-coverage was below a threshold of 32.5 Gy in 30% of volunteers (30.6 Gy, 32.0 Gy, 32.3 Gy).


The dosimetric benefit of MR-guided online adaptation for prostate SBRT was robust over 45 min in all volunteers. However, intrafractional uncertainties became dosimetrically relevant at 60 min and we therefore recommend verification imaging before delivery of MR-guided online adapted SBRT.


Stereotactic body radiotherapy (SBRT) has been implemented in the treatment of localized prostate cancer and evaluated in multiple prospective phase II trials, which have shown comparable outcomes to other treatment modalities both, with regard to toxicities, and to long-term recurrence-free survival [1,2,3,4]. Consequently, SBRT today represents an alternative to conventionally fractionated radiotherapy for low to intermediate risk prostate cancer at clinics with appropriate technology, physics, and clinical expertise according to the NCCN guidelines v2.2020 [5,6,7].

With higher doses per fraction comes the necessity of accurate dose-delivery, conformal to the target and adjusted to the changing anatomy of the small pelvis. Magnetic resonance (MR)-guided radiotherapy with daily adaptation has the potential to improve the precision and accuracy of radiotherapy through continuous tracking of the target volume and image-guidance with improved soft-tissue contrast and anatomic visualization compared to cone-beam computer tomography (CBCT) scans [8]. Daily online plan-adaptation can yield reduced planning target volume (PTV) margins by accounting for movements in both, the clinical target volume (CTV) and organs at risk (OAR) in close proximity. It promises to compensate for both, systematic anatomic changes, like prostate swelling, as well as random changes, such as inter- and intrafractional rectal and bladder fillings.

Prior to the availability of MR-guided online adaptation, stereotactic treatment plans for prostate cancer were not routinely adapted online, mainly due to the length of the planning process and the insufficient soft tissue contrast of CBCT. MR-guided linear accelerators are now commercially available offering continuous visualization and online adaptation. However, the workflow to perform this adaptation has been reported to be in the range of 50 min, which is in agreement with our own experiences [9,10,11,12].

During this time, bladder filling, peristalsis and air passing through the rectum may be sources of significant changes in the immediate anatomy of the prostate. The aim of this study was therefore to analyze the dosimetric benefit of performing an MR-guided online adaptation in SBRT for prostate cancer and to elucidate its stability.


Ten healthy male volunteers (27–51 years of age, median 35) were recruited and scanned in the ViewRay® MR-linear accelerator (ViewRay® Inc., Mountain View, CA) at the University Hospital Zurich at two different timepoints. All volunteers had previously consented to participate in this study. Ethical review and approval was acquired from the cantonal ethics committee Zurich (2021-00158).

For immobilization, a headrest and a Knee-Fix were used. On day one, volunteers were positioned for a mock prostate SBRT treatment in the MR-Linac. Set-up images were acquired in low resolution, and the couch was shifted to the expected isocenter located within the prostate. A 3D-simulation high-resolution MR-scan (with 0.15 cm resolution during a 128–173-s image acquisition with a field of view 40 × 43 × 40) was acquired in free breathing. True FISP (fast imaging with steady state procession) sequences were acquired using balanced gradients. A baseline prostate SBRT plan was created according to the workflow described below.

On a different day, the volunteers were positioned identically in the MR-Linac and another low-resolution MR-scan was acquired for set-up. The prostate position was registered in AP, LR and SI direction between the baseline scan and the verification scan to compensate for interfractional translational shifts of the prostate position, and the couch was shifted accordingly. By correcting these translation shifts, we were able to independently analyze the effect of rotational errors as well as deformations of the prostate. The baseline SBRT plan was copied onto the first MR of the day and was subsequently optimized to create the plan-of-the-day using identical IMRT planning objectives as at baseline. Over 1 h, we acquired additional high-resolution MR scans in 15 min intervals in treatment position to analyze the stability of the adapted plan over these 60 min. For every consecutive MR-scan, a registration of the prostate in translational AP, LR and SI directions was performed, and the couch was shifted accordingly. The shifts are shown in Additional file 1: Table S1. The adapted plan was then copied onto the consecutive MR-scans and was recalculated on the anatomy from the consecutive MR-scans obtained after 15, 30, 45, and 60 min (MR2-5).

The target volume included the healthy prostate and the lower third of the seminal vesicles, which were contoured by one physician (JS) using MIMvista software as the clinical target volume (CTV), and a margin of 5 mm (3 mm posteriorly towards the rectum) was added to form the planning target volume (PTV). OAR including the entire rectum (not rectum wall), entire bladder, penile bulb, and femur heads were contoured for all volunteers at all timepoints. Contours were propagated and adjusted to changes of volume and shape over time. The workflow is outlined in Fig. 1. Of note, we abstained from bladder or rectum filling regimens, and folly catheters for the healthy volunteers.

Fig. 1

The workflow

Fractionation, plan evaluation and analysis

A dose of 36.25 Gy in 5 fractions (equal to an estimated 2 Gy-equivalent dose of 90.5 Gy for an alpha/beta value of 1.5) was prescribed to the planning target volume to cover 95% of the PTV with 95% of the prescribed dose. PTV and OAR constraints are shown in Additional file 2: Table S2. We deemed a threshold of 32.5 Gy to be the minimally acceptable D95CTV according to Kishan et al. as their study represented a similar dosing regimen to this study [1]. 32.5 Gy in 5 fractions is equivalent to an EQD2 dose of 74 Gy, assuming an alpha/beta value of 1.5. This dose is considered as the minimum dose in a curative setting in conventional fractionation.

A 9-field step-and-shoot IMRT plan was calculated with the ViewRay® Planning System using 6 MV flattening filter free photons with a maximum dose rate of 600 MU/min; dose calculation used Monte Carlo with a statistical uncertainty of 1% and grid spacing of 3 mm. All plans were verified with the MR-compatible Delta 4 Phantom (ScandiDos, Uppsala, Sweden) and passed with a gamma criterion of 3% 3 mm with a passing rate above 95%.

In order to compare the different plans, all treatment plans were transferred into MIM-software® (MIM-software® Inc., Cleveland, OH) and dose volume histograms were exported for evaluation.

Statistical analyses were performed with GraphPad Prism software version 8.2.0. Distribution of data was assumed to be non-Gaussian and therefore only non-parametric tests were applied. For comparing the difference in absolute dose to different targets, Wilcoxon matched pairs signed rank test was used. A p value of 0.05 was deemed to be statistically significant.


Online adaptive re-planning

Image quality of the MR-scans was deemed sufficient for baseline planning and adaptive re-planning in all volunteers and at all timepoints by a highly experienced medical physicist and a radiation oncologist experienced in MR-based prostate delineation. Both, CTV- and PTV-coverage were improved by MR-guided online adaptation in 90% of volunteers (Fig. 2 baseline vs. adapted plan D95CTV, Table 1).

Fig. 2

Dosimetric benefit of adaptation compared to original plan A, B median D95CTV and D95PTV comparison of absolute doses with blue = baseline plan and orange = adapted plan C, D dose volume histograms for D95CTV and D95PTV for blue = baseline plan and orange = adapted plan

Table 1 Comparison of absolute dose (Gy) for organs at risk and coverage for the baseline plan on the MR of the day versus the adapted plan for ten volunteers

The median D95CTV- and D95PTV-coverage was improved from 34.8 to 35.5 Gy (p = 0.006) and 31.4 to 34.6 Gy (p = 0.005), respectively. Online adaptive re-planning with recovery of target coverage was not associated with higher doses to the OAR, most importantly the rectum (Additional file 3: Fig. S1). The median D1ccrectum was lower in the adapted plans compared to the baseline plan copied onto the MR of the day with 33.33 Gy versus 32.3 Gy. Similar results were observed for the Dmeanbladder (9.6 Gy vs. 8.8 Gy, Table 1).

Stability of online adapted SBRT plans

Repetitive MR-scans were acquired for ten volunteers in 15 min intervals for a total duration of 60 min. There was no systematic shift in any direction and at any timepoint larger than 2 mm. The 3D vectors of intrafractional prostate drifts at timepoints 15, 30, 45 and 60 min were 1.2 mm, 1.6 mm, 1.0 mm and 0.4 mm, respectively. Full shifting data is displayed in Additional file 1: Table S1.

For assessment of recalculated plans at 15, 30, 45 and 60 min, we defined a threshold of 32.5 Gy as the minimally acceptable D95CTV, which represents 74 Gy EQD2Gy assuming an alpha/beta value of 1.5 Gy [13]. Consider that all translational drifts of the prostate have been corrected before dose re-calculation. The median D95CTV remained stable (0 min: 35.5 Gy, 60 min: 35.3 Gy) and the difference compared to baseline remained statistically non-significant for all timepoints (p = 0.26 for timepoint 0 vs. timepoint 60 min). Target coverage remained above this threshold for all ten volunteers at timepoints 15, 30 and 45 min (Fig. 3). At 60 min, three volunteers had an unacceptable D95CTV below the threshold of 32.5 Gy due to non-rigid anatomical deformations. With respect to doses to OAR, the Dmeanbladder decreased significantly over the one-hour time period due to increasing filling (Fig. 4A p = 0.01 timepoint 0 vs. timepoint 60 min). The D1ccrectum did not differ between timepoint 0 and 60 min (Fig. 4B p = 0.59).

Fig. 3

Absolute D95CTV of adapted plan over 1 h in 15 min intervals for ten volunteers. The bars depict the median dose. The dotted line represents the minimally acceptable D95CTV threshold dose

Fig. 4

A Dmeanbladder and B D1ccrectum of ten volunteers over 1 h in 15 min intervals. The bars depict the median dose


This analysis shows that MR-guided online adaptation of SBRT for prostate cancer achieves a dosimetric benefit that is stable over the time currently required for this complex and multi-professional process and may yield clinical benefits. However, caution should be taken, because larger non-rigid intrafractional variations were observed in few volunteers, which resulted in decreasing target coverage at 60 min. We therefore recommend a verification MR-scan after the plan adaption process and before SBRT delivery to assess stability of the adapted treatment plan as a standard procedure.

We showed that a better target coverage was not associated with higher dose to the OAR, most importantly the rectum. Here, we would like to stress that we delineated the entire organ and not just the rectum and bladder wall as an OAR and therefore hotspots could have been located in the lumen not contributing to possible clinical toxicity. In future, delineation of rectum or bladder wall may be considered in MR-based planning.

To date, the stability of MR-guided adaptation benefit for prostate SBRT over time has only been investigated in a small number of patients (n = 5) treated with 20 × 3.1 Gy by de Muinck Keizer et al. [14]. During the on-couch period of 45 min in accordance with our assumptions, the group showed that the variance of intrafraction motions grows over time but that margins do not need to be increased beyond 5 mm. The group had formerly investigated intrafractional motion during prostate MR-guided SBRT using four implanted gold fiducial markers [15]. Here, they reported movements of the markers at ten minutes of X: 0.0 ± 0.8 mm; Y: 1.0 ± 1.9 mm and Z: 0.9 ± 2 mm, as well as mean rotation of X: 0.1 ± 3.0°, Y: 0.0 ± 1.3° and Z: 0.1 ± 1.2°. However, the dosimetric consequences were not analyzed and the time frame was rather short with ten minutes. Before MR-guided radiotherapy was available, inter- and intrafractional motion has been described using electromagnetic transponders (Calypso® system) and gold markers [16,17,18,19,20,21,22,23]. In these studies, maximal mean interfractional motion of the prostate varied between 3.1 and 5 mm. For intrafractional motion, studies showed both, persistent drifts and rapid movements with varying reports of > 5 mm deviations in 15% of cases to intrafractional changes of < 1 mm in all cases.

Real-time tracking and adaptation has recently become semi-automated as an algorithm proposed by Olsen et al. shows [24]. The authors have described a method that reduced the workload of adaptive planning and included compensation for both, translational and rotational movements—however the authors point out that fiducial geometry and axis of rotation has large impact on interpreting tracking data. While this algorithm is able to facilitate tracking, implanting the required markers remains an invasive method, which poses interventional risks such as bleeding and infection, possibly superfluous with this advanced image guidance.

A recent phase III study comparing normofractionated, hypofractionated and stereotactic radiotherapy for low to intermediate risk prostate cancer showed no increase in toxicity for SBRT compared to hypofractionation, although long-term data is still lacking [25]. However, image-guidance and adaptive planning may yield clinical relevance through reducing margins in light of the development towards even more extreme hypofractionation which are associated with higher risk for toxicities. A recent phase I dose escalation trial concluded that 36 Gy in only 4 fractions (with a 2-day break between fractions) prescribed at the 95% isodose level is recommendable with an acceptable toxicity profile [26]. Of note, the authors did not report the image-guidance that was available to them for delivery of single doses of 8–9 Gy. Potter and colleagues investigated delivering up to 50 Gy in 5 fractions using a Calypso-based system and kV and CBCT-image guidance in a phase I trial with an improved PSA-nadir for 45–50 Gy total dose without higher incidence of grade 3 toxicity [27]. Studies evaluating even single-fraction SBRT are currently enrolling patients [28].

Multiple treatment regimens for all stages of prostate cancer are currently vigorously examined by a multitude of phase I–III trials (One-Shot NCT03294889, PRIME NCT03561961, PATRIOT [29] and others). First clinical experience shows favorable quality of life for patients treated with MR-guided SBRT for prostate cancer [12].

All new hypofractionated treatment regimens have in common the need for daily imaging to minimize toxicity and avoid underdosing of target volumes highlighting the future utility of MR-guided online adaptation systems.

The limitations of this study include its single center character, the relatively small sample size, the omission of a bladder or rectum protocol, as well as Foley catheters in this set of volunteers that was younger than the usual patient cohort.

A bladder and rectum protocol, as well as Foley catheters were omitted, because albeit side effects of these interventions are rare, we did not wish to expose the healthy volunteers to any risks. We acknowledge, that this might present a deviation from clinical practice; however, the clinical benefit of a bladder and rectum preparation protocol remains uncertain and has not been validated in randomized trials [30, 31]. From an anatomical and dosimetric perspective, rectum filling and bladder filling do influence the doses delivered to these organs at risk. An empty rectum and a full bladder would be optimal for OAR sparing. However, the reproducibility especially of a filled bladder during a course of fractionated radiotherapy is an issue of concern.

Importantly, the volunteers were younger (median age 35 years) than the average prostate cancer patient, which may result in higher compliance and fewer internal anatomical shifts. While constipation or flatulence might be more common in an older age group (although data supporting this are missing), in clinical practice, the bladder or rectum protocol would be in place to at least alleviate the effects. Due to the possibility of target and OAR shifts over time, it is of utmost importance to perform imaging and treatment as promptly as is safely possible.

This study does not unequivocally imply a clinical benefit for patients. The small sham trial was not designed to prove such clinical benefit. The study does, however, show dosimetric benefits that may translate to clinical benefits. Larger studies designed to show a clinical benefit will need to examine whether that hypothesis holds true.

In conclusion, when performing prostate SBRT, daily imaging is of utmost importance due to interfractional anatomic variability. Daily plan-adaptation yields significant dosimetric and potentially clinically relevant benefits, that are stable over at least 45 min. Crucially, outliers exist with large intrafractional deformations and given the lack of markers to identify these movers prospectively, a MR verification scan before dose-delivery is highly recommended to ensure exact treatment. In the future, faster and possibly (semi-) automated adaptation workflows, or continuous imaging could speed up the adaptation process, reducing the relevance of intrafractional motion during adaptation.

Availability of data and materials

The dataset(s) supporting the conclusions of this article is(are) included within the article (and its additional file(s)).


  1. 1.

    Kishan AU, Dang A, Katz AJ, et al. Long-term outcomes of stereotactic body radiotherapy for low-risk and intermediate-risk prostate cancer. JAMA Netw Open. 2019;2:e188006.

    Article  Google Scholar 

  2. 2.

    Alayed Y, Cheung P, Chu W, et al. Two StereoTactic ablative radiotherapy treatments for localized prostate cancer (2STAR): results from a prospective clinical trial. Radiother Oncol. 2019;135:86–90.

    Article  Google Scholar 

  3. 3.

    Jackson WC, Silva J, Hartman HE, et al. Stereotactic body radiation therapy for localized prostate cancer: a systematic review and meta-analysis of over 6000 patients treated on prospective studies. Int J Radiat Oncol Biol Phys. 2019;104:778–89.

    Article  Google Scholar 

  4. 4.

    Widmark A, Gunnlaugsson A, Beckman L, et al. Ultra-hypofractionated versus conventionally fractionated radiotherapy for prostate cancer: 5-year outcomes of the HYPO-RT-PC randomised, non-inferiority, phase 3 trial. Lancet (London, England). 2019;394:385–95.

    Article  Google Scholar 

  5. 5.

    Freedman-Cass D, Shead DA, Schaeffer E, et al. NCCN Guidelines Panel Disclosures Continue ф Diagnostic/Interventional Radiology Þ Internal medicine † Medical oncology ≠ Pathology ¥ Patient advocate § Radiotherapy/Radiation oncology w Urology * Discussion Section Writing Committee NCCN Guidelines Versi. 2020.

  6. 6.

    Katz AJ, Santoro M, Diblasio F, Ashley R. Stereotactic body radiotherapy for localized prostate cancer: disease control and quality of life at 6 years. Radiat Oncol. 2013;8:118.

    CAS  Article  Google Scholar 

  7. 7.

    Moon DH, Efstathiou JA, Chen RC. What is the best way to radiate the prostate in 2016? Urol Oncol. 2017;35:59–68.

    Article  Google Scholar 

  8. 8.

    Noel CE, Parikh PJ, Spencer CR, Green OL, Hu Y, Mutic S, Olsen JR. Comparison of onboard low-field magnetic resonance imaging versus onboard computed tomography for anatomy visualization in radiotherapy. Acta Oncol (Madr). 2015;54:1474–82.

    Article  Google Scholar 

  9. 9.

    Sahin B, Zoto Mustafayev T, Gungor G, Aydin G, Yapici B, Atalar B, Ozyar E. First 500 fractions delivered with a magnetic resonance-guided radiotherapy system: initial experience. Cureus. 2019.

    Article  PubMed  PubMed Central  Google Scholar 

  10. 10.

    Finazzi T, Palacios MA, Spoelstra FOB, Haasbeek CJA, Bruynzeel AME, Slotman BJ, Lagerwaard FJ, Senan S. Role of on-table plan adaptation in MR-guided ablative radiation therapy for central lung tumors. Int J Radiat Oncol Biol Phys. 2019;104:933–41.

    Article  Google Scholar 

  11. 11.

    Patel KR, Chowdhary M, Switchenko JM, Kudchadkar R, Lawson DH, Cassidy RJ, Prabhu RS, Khan MK. BRAF inhibitor and stereotactic radiosurgery is associated with an increased risk of radiation necrosis. Melanoma Res. 2016;26:387–94.

    CAS  Article  Google Scholar 

  12. 12.

    Alongi F, Rigo M, Figlia V, et al. 1.5 T MR-guided and daily adapted SBRT for prostate cancer: feasibility, preliminary clinical tolerability, quality of life and patient-reported outcomes during treatment. Radiat Oncol. 2020.

    Article  PubMed  PubMed Central  Google Scholar 

  13. 13.

    Dearnaley D, Syndikus I, Mossop H, et al. Conventional versus hypofractionated high-dose intensity-modulated radiotherapy for prostate cancer: 5-year outcomes of the randomised, non-inferiority, phase 3 CHHiP trial. Lancet Oncol. 2016;17:1047–60.

    Article  Google Scholar 

  14. 14.

    de Muinck Keizer DM, Kerkmeijer LGW, Willigenburg T, van Lier ALHMW, de Hartogh MD, van der Voort van Zyp JRN, de Groot-van Breugel EN, Raaymakers BW, Lagendijk JJW, de Boer JCJ. Prostate intrafraction motion during the preparation and delivery of MR-guided radiotherapy sessions on a 1.5 T MR-Linac. Radiother Oncol. 2020;151:88–94.

    Article  Google Scholar 

  15. 15.

    de Muinck Keizer DM, Pathmanathan AU, Andreychenko A, Kerkmeijer LGW, van der Voort van Zyp JRN, Tree AC, van den Berg CAT, de Boer JCJ. Fiducial marker based intra-fraction motion assessment on cine-MR for MR-linac treatment of prostate cancer. Phys Med Biol. 2019;64:07NT02.

    Article  Google Scholar 

  16. 16.

    Kupelian P, Willoughby T, Mahadevan A, et al. Multi-institutional clinical experience with the Calypso System in localization and continuous, real-time monitoring of the prostate gland during external radiotherapy. Int J Radiat Oncol Biol Phys. 2007;67:1088–98.

    Article  Google Scholar 

  17. 17.

    Willoughby TR, Kupelian PA, Pouliot J, et al. Target localization and real-time tracking using the Calypso 4D localization system in patients with localized prostate cancer. Int J Radiat Oncol Biol Phys. 2006;65:528–34.

    Article  Google Scholar 

  18. 18.

    Nederveen AJ, van der Heide UA, Dehnad H, van Moorselaar RJA, Hofman P, Lagendijk JJW. Measurements and clinical consequences of prostate motion during a radiotherapy fraction. Int J Radiat Oncol Biol Phys. 2002;53:206–14.

    Article  Google Scholar 

  19. 19.

    Aubry JF, Beaulieu L, Girouard LM, Aubin S, Tremblay D, Laverdière J, Vigneault E. Measurements of intrafraction motion and interfraction and intrafraction rotation of prostate by three-dimensional analysis of daily portal imaging with radiopaque markers. Int J Radiat Oncol Biol Phys. 2004;60:30–9.

    Article  Google Scholar 

  20. 20.

    Chen J, Lee RJ, Handrahan D, Sause WT. Intensity-modulated radiotherapy using implanted fiducial markers with daily portal imaging: assessment of prostate organ motion. Int J Radiat Oncol Biol Phys. 2007;68:912–9.

    Article  Google Scholar 

  21. 21.

    Britton KR, Takai Y, Mitsuya M, Nemoto K, Ogawa Y, Yamada S. Evaluation of inter- and intrafraction organ motion during intensity modulated radiation therapy (IMRT) for localized prostate cancer measured by a newly developed on-board image-guided system. Radiat Med. 2005;23:14–24.

    PubMed  Google Scholar 

  22. 22.

    Kotte ANTJ, Hofman P, Lagendijk JJW, van Vulpen M, van der Heide UA. Intrafraction motion of the prostate during external-beam radiation therapy: analysis of 427 patients with implanted fiducial markers. Int J Radiat Oncol Biol Phys. 2007;69:419–25.

    Article  Google Scholar 

  23. 23.

    Madsen BL, Hsi RA, Pham HT, Presser J, Esagui L, Corman J, Myers L, Jones D, Fowler JF. Intrafractional stability of the prostate using a stereotactic radiotherapy technique\rStereotactic hypofractionated accurate radiotherapy of the prostate (SHARP), 33.5 Gy in five fractions for localized disease: first clinical trial results. Int J Radiat Oncol Biol Phys. 2003;57:1285–91.

    Article  Google Scholar 

  24. 24.

    Olsen JR, Noel CE, Baker K, Santanam L, Michalski JM, Parikh PJ. Practical method of adaptive radiotherapy for prostate cancer using real-time electromagnetic tracking. Int J Radiat Oncol Biol Phys. 2012;82:1903–11.

    Article  Google Scholar 

  25. 25.

    Brand DH, Tree AC, Ostler P, et al. Intensity-modulated fractionated radiotherapy versus stereotactic body radiotherapy for prostate cancer (PACE-B): acute toxicity findings from an international, randomised, open-label, phase 3, non-inferiority trial. Lancet Oncol. 2019;20:1531–43.

    Article  Google Scholar 

  26. 26.

    Kainuma T, Kawakami S, Tsumura H, Satoh T, Tabata K, Iwamura M, Hayakawa K, Ishiyama H. A phase I dose-escalation trial of stereotactic body radiotherapy using 4 fractions for patients with localized prostate cancer. Radiat Oncol. 2019;14:158.

    Article  Google Scholar 

  27. 27.

    Potters L, Rana Z, Lee L, Cox BW. Outcomes of a dose-escalated stereotactic body radiation phase 1 trial for patients with low- and intermediate-risk prostate cancer. Int J Radiat Oncol Biol Phys. 2019;104:334–42.

    Article  Google Scholar 

  28. 28.

    Zilli T, Franzese C, Bottero M, et al. Single fraction urethra-sparing prostate cancer SBRT: phase I results of the ONE SHOT trial. Radiother Oncol. 2019;139:83–6.

    Article  Google Scholar 

  29. 29.

    Quon HC, Ong A, Cheung P, et al. Once-weekly versus every-other-day stereotactic body radiotherapy in patients with prostate cancer (PATRIOT): a phase 2 randomized trial. Radiother Oncol. 2018;127:206–12.

    Article  Google Scholar 

  30. 30.

    McGuffin M, Devji N, Kehoe L, et al. To prep or not to prep—that is the question: a randomized trial on the use of antiflatulent medication as part of bowel preparation for patients having image guided external beam radiation therapy to the prostate. Pract Radiat Oncol. 2018;8:116–22.

    Article  Google Scholar 

  31. 31.

    Mullaney LM, O’Shea E, Dunne MT, Finn MA, Thirion PG, Cleary LA, McGarry M, O’Neill L, Armstrong JG. A randomized trial comparing bladder volume consistency during fractionated prostate radiation therapy. Pract Radiat Oncol. 2014;4:e203–12.

    Article  Google Scholar 

Download references


The authors would like to cordially thank all volunteers from the University Hospital Zurich Radiation Oncology Department.


No funding was obtained for this study.

Author information




JS, NA, STL, MG: conceptualization, study draft; JS, MM, MC, LW, MB, MZ, JK: data acquisition; JS, MC, STL: formal analysis; JS: lead writing, all others: manuscript review and editing. All authors read and approved the final manuscript.

Corresponding author

Correspondence to J. Schaule.

Ethics declarations

Ethics approval

Ethical review and approval was obtained from the cantonal ethics commission Zurich (2021-00158).

Consent for publication

Not applicable.

Competing interests

All authors declare no conflicts of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Table S1.

Couch shifts; A lateral, B vertical, C axial shifts in cm. Each line represents one volunteer. Bold = median.

Additional file 2: Table S2.

Dose Constraints.

Additional file 3: Fig. S1.

D1ccrectum for the baseline plan on the MR of the day compared to the adapted plan. Bar = median.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Schaule, J., Chamberlain, M., Wilke, L. et al. Intrafractional stability of MR-guided online adaptive SBRT for prostate cancer. Radiat Oncol 16, 189 (2021).

Download citation


  • MR-guided radiotherapy
  • Online adaptation
  • Prostate SBRT
  • Plan-of-the-day