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The patterns of care, tolerability and safety in the first year of a novel high field MR-linac

van Otterloo, S. R. D.
Christodouleas, J. P.
Blezer, E. L. A.
Cobben, David
Erickson, B. A.
Fuller, C. D.
Hafeez, S.
Kirby, A.
Lalondrelle, S.
Mook, S.
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Abstract
Purpose/Objective(s): High field MR-Linacs are promising because they may enable unique anatomic and response adaptive treatment paradigms. The first commercial device received regulatory approval in late 2018. Because high field MR-guided therapy is new, little is known about how clinicians are using it, how patients tolerate daily high field MRIs and the toxicity patterns of such treatments. Herein we report the first years’ experience within an international registry study (MOMENTUM). Materials/Methods: The MOMENTUM Study (NCT04075305), a project of the MR-Linac Consortium, is an international registry that collects clinical and technical patient data with informed consent. All patients treated on an MR-Linac at participating centers are eligible. We reviewed the experience of patients treated from Dec. 5th 2018 to Jan. 15th 2020 and used descriptive statistics to describe the patterns of care, tolerability (defined as the percent of patients discontinuing the MR-Linac course early) and safety (defined by grade 3-5 CTCAE v.5 acute toxicity within 3 months of the end of treatment). Results: The study cohort includes 393 patients treated at seven institutions in four countries (Netherlands, U.K., U.S. and Canada) and represents over 50% of all patients treated globally with high field MRguided therapy in the first year after regulatory approval. Median age was 68 years (range 29-93 years) and 78% were male. There were 23 different tumor sites treated the most common being prostate (32%), lymph node oligometastases (20%), rectum (11%), brain (7%), and oropharynx (6%). Radiation of the primary tumor (71%) was the most common clinical indication followed by regional lymph node (19%), distant metastases (8%) and cancer recurrence at the primary tumor site (2%). In the total cohort, 51% (150/395) had contours adjusted with every fraction (adapt-toshape). In the subset for whom complete course of therapy data was available (n Z 228), the median number of fractions per course was 5 (range: 1-35) and 97% (222/228) had radiotherapy on the MR-Linac only. Two (1%) MR-Linac courses were discontinued early. One discontinuation was due to technical problems and in one case the treating physician decided to discontinue treatment after disease progression on imaging and clinical decline of the patient. In the subset for whom complete acute toxicity data was available (nZ97), acute grade 3 toxicity occurred in 4% and grade 4-5 toxicities were not observed. Conclusion: In the first year after initial regulatory approval of high field MR-guided therapy, we observed a wide variety of treatment sites and indications. Daily high field MR was well tolerated and our initial acute toxicity assessment was reassuring.
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2020
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Meetings and Proceedings
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van Otterloo SRD, Christodouleas JP, Blezer ELA, Cobben D, Erickson BA, Fuller CD, et al. The patterns of care, tolerability and safety in the first year of a novel high field MR-linac. International Journal of Radiation Oncology Biology Physics. 2020;108(3):S65-S
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