Quantitating Interfraction Target Dynamics During Concurrent Chemoradiation for Glioblastoma: A Prospective Serial Imaging Study
Magnetic resonance image (MRI) guided radiation therapy has the potential to improve outcomes for glioblastoma by adapting to tumor changes during radiation therapy. This study quantifies interfraction dynamics (tumor size, position, and geometry) based on sequential magnetic resonance imaging scans...
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Published in | International journal of radiation oncology, biology, physics Vol. 109; no. 3; pp. 736 - 746 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
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Language | English |
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Elsevier Inc
01.03.2021
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Abstract | Magnetic resonance image (MRI) guided radiation therapy has the potential to improve outcomes for glioblastoma by adapting to tumor changes during radiation therapy. This study quantifies interfraction dynamics (tumor size, position, and geometry) based on sequential magnetic resonance imaging scans obtained during standard 6-week chemoradiation.
Sixty-one patients were prospectively imaged with gadolinium-enhanced T1 (T1c) and T2/FLAIR axial sequences at planning (Fx0), fraction 10 (Fx10), fraction 20 (Fx20), and 1 month after the final fraction of chemoradiation therapy (P1M). Gross tumor volumes (GTVs) and clinical target volumes (CTVs) were contoured at all time points. Target dynamics were quantified by absolute volume (V), volume relative to Fx0 (Vrel), and the migration distance (dmigrate; the linear displacement of the GTV or CTV relative to Fx0). Temporal changes were assessed using a linear mixed-effects model.
Median volumes at Fx0, Fx10, Fx20, and P1M for the GTV were 18.4 cm3 (range, 1.1–110.5 cm3), 14.7 cm3 (range, 0.9–115.1 cm3), 13.7 cm3 (range, 0.6–174.2 cm3), and 13.0 cm3 (range, 0.9–76.3 cm3), respectively, with corresponding median Vrel of 0.88 at Fx10, 0.77 at Fx20, and 0.71 at P1M relative to Fx0 (P < .001 for all). The GTV (CTV) migration distances were greater than 5 mm in 46% (54%) of patients at Fx10, 50% (58%) of patients at Fx20, and 52% (57%) of patients at P1M. Dynamic tumor morphologic changes were observed, with 40% of patients exhibiting a decreased GTV (Vrel ≤1) with a dmigrate >5 mm during chemoradiation therapy.
Clinically meaningful tumor dynamics were observed during chemoradiation therapy for glioblastoma, supporting evaluation of daily MRI guided radiation therapy and treatment plan adaptation. |
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AbstractList | Magnetic resonance image (MRI) guided radiation therapy has the potential to improve outcomes for glioblastoma by adapting to tumor changes during radiation therapy. This study quantifies interfraction dynamics (tumor size, position, and geometry) based on sequential magnetic resonance imaging scans obtained during standard 6-week chemoradiation. Magnetic resonance image (MRI) guided radiation therapy has the potential to improve outcomes for glioblastoma by adapting to tumor changes during radiation therapy. This study quantifies interfraction dynamics (tumor size, position, and geometry) based on sequential magnetic resonance imaging scans obtained during standard 6-week chemoradiation. Sixty-one patients were prospectively imaged with gadolinium-enhanced T1 (T1c) and T2/FLAIR axial sequences at planning (Fx0), fraction 10 (Fx10), fraction 20 (Fx20), and 1 month after the final fraction of chemoradiation therapy (P1M). Gross tumor volumes (GTVs) and clinical target volumes (CTVs) were contoured at all time points. Target dynamics were quantified by absolute volume (V), volume relative to Fx0 (Vrel), and the migration distance (dmigrate; the linear displacement of the GTV or CTV relative to Fx0). Temporal changes were assessed using a linear mixed-effects model. Median volumes at Fx0, Fx10, Fx20, and P1M for the GTV were 18.4 cm3 (range, 1.1–110.5 cm3), 14.7 cm3 (range, 0.9–115.1 cm3), 13.7 cm3 (range, 0.6–174.2 cm3), and 13.0 cm3 (range, 0.9–76.3 cm3), respectively, with corresponding median Vrel of 0.88 at Fx10, 0.77 at Fx20, and 0.71 at P1M relative to Fx0 (P < .001 for all). The GTV (CTV) migration distances were greater than 5 mm in 46% (54%) of patients at Fx10, 50% (58%) of patients at Fx20, and 52% (57%) of patients at P1M. Dynamic tumor morphologic changes were observed, with 40% of patients exhibiting a decreased GTV (Vrel ≤1) with a dmigrate >5 mm during chemoradiation therapy. Clinically meaningful tumor dynamics were observed during chemoradiation therapy for glioblastoma, supporting evaluation of daily MRI guided radiation therapy and treatment plan adaptation. PURPOSEMagnetic resonance image (MRI) guided radiation therapy has the potential to improve outcomes for glioblastoma by adapting to tumor changes during radiation therapy. This study quantifies interfraction dynamics (tumor size, position, and geometry) based on sequential magnetic resonance imaging scans obtained during standard 6-week chemoradiation. METHODS AND MATERIALSSixty-one patients were prospectively imaged with gadolinium-enhanced T1 (T1c) and T2/FLAIR axial sequences at planning (Fx0), fraction 10 (Fx10), fraction 20 (Fx20), and 1 month after the final fraction of chemoradiation therapy (P1M). Gross tumor volumes (GTVs) and clinical target volumes (CTVs) were contoured at all time points. Target dynamics were quantified by absolute volume (V), volume relative to Fx0 (Vrel), and the migration distance (dmigrate; the linear displacement of the GTV or CTV relative to Fx0). Temporal changes were assessed using a linear mixed-effects model. RESULTSMedian volumes at Fx0, Fx10, Fx20, and P1M for the GTV were 18.4 cm3 (range, 1.1-110.5 cm3), 14.7 cm3 (range, 0.9-115.1 cm3), 13.7 cm3 (range, 0.6-174.2 cm3), and 13.0 cm3 (range, 0.9-76.3 cm3), respectively, with corresponding median Vrel of 0.88 at Fx10, 0.77 at Fx20, and 0.71 at P1M relative to Fx0 (P < .001 for all). The GTV (CTV) migration distances were greater than 5 mm in 46% (54%) of patients at Fx10, 50% (58%) of patients at Fx20, and 52% (57%) of patients at P1M. Dynamic tumor morphologic changes were observed, with 40% of patients exhibiting a decreased GTV (Vrel ≤1) with a dmigrate >5 mm during chemoradiation therapy. CONCLUSIONSClinically meaningful tumor dynamics were observed during chemoradiation therapy for glioblastoma, supporting evaluation of daily MRI guided radiation therapy and treatment plan adaptation. Magnetic resonance image (MRI) guided radiation therapy has the potential to improve outcomes for glioblastoma by adapting to tumor changes during radiation therapy. This study quantifies interfraction dynamics (tumor size, position, and geometry) based on sequential magnetic resonance imaging scans obtained during standard 6-week chemoradiation. Sixty-one patients were prospectively imaged with gadolinium-enhanced T1 (T1c) and T2/FLAIR axial sequences at planning (Fx0), fraction 10 (Fx10), fraction 20 (Fx20), and 1 month after the final fraction of chemoradiation therapy (P1M). Gross tumor volumes (GTVs) and clinical target volumes (CTVs) were contoured at all time points. Target dynamics were quantified by absolute volume (V), volume relative to Fx0 (V ), and the migration distance (d ; the linear displacement of the GTV or CTV relative to Fx0). Temporal changes were assessed using a linear mixed-effects model. Median volumes at Fx0, Fx10, Fx20, and P1M for the GTV were 18.4 cm (range, 1.1-110.5 cm ), 14.7 cm (range, 0.9-115.1 cm ), 13.7 cm (range, 0.6-174.2 cm ), and 13.0 cm (range, 0.9-76.3 cm ), respectively, with corresponding median V of 0.88 at Fx10, 0.77 at Fx20, and 0.71 at P1M relative to Fx0 (P < .001 for all). The GTV (CTV) migration distances were greater than 5 mm in 46% (54%) of patients at Fx10, 50% (58%) of patients at Fx20, and 52% (57%) of patients at P1M. Dynamic tumor morphologic changes were observed, with 40% of patients exhibiting a decreased GTV (V ≤1) with a d >5 mm during chemoradiation therapy. Clinically meaningful tumor dynamics were observed during chemoradiation therapy for glioblastoma, supporting evaluation of daily MRI guided radiation therapy and treatment plan adaptation. |
Author | Soliman, Hany Myrehaug, Sten Das, Sunit Campbell, Mikki Chen, Hanbo Perry, James Sahgal, Arjun Ruschin, Mark Atenafu, Eshetu G. Maralani, Pejman Jabehdar Stewart, James Lee, Young Detsky, Jay Husain, Zain Ho, Ling Stanisz, Greg Lau, Angus Z. Tseng, Chia-Lin Lipsman, Nir |
Author_xml | – sequence: 1 givenname: James surname: Stewart fullname: Stewart, James organization: Department of Radiation Oncology, Sunnybrook Odette Cancer Centre, Toronto, Canada – sequence: 2 givenname: Arjun surname: Sahgal fullname: Sahgal, Arjun organization: Department of Radiation Oncology, Sunnybrook Odette Cancer Centre, Toronto, Canada – sequence: 3 givenname: Young surname: Lee fullname: Lee, Young organization: Department of Radiation Oncology, University of Toronto, Toronto, Canada – sequence: 4 givenname: Hany surname: Soliman fullname: Soliman, Hany organization: Department of Radiation Oncology, Sunnybrook Odette Cancer Centre, Toronto, Canada – sequence: 5 givenname: Chia-Lin surname: Tseng fullname: Tseng, Chia-Lin organization: Department of Radiation Oncology, Sunnybrook Odette Cancer Centre, Toronto, Canada – sequence: 6 givenname: Jay surname: Detsky fullname: Detsky, Jay organization: Department of Radiation Oncology, Sunnybrook Odette Cancer Centre, Toronto, Canada – sequence: 7 givenname: Zain surname: Husain fullname: Husain, Zain organization: Department of Radiation Oncology, Sunnybrook Odette Cancer Centre, Toronto, Canada – sequence: 8 givenname: Ling surname: Ho fullname: Ho, Ling organization: Department of Radiation Oncology, Sunnybrook Odette Cancer Centre, Toronto, Canada – sequence: 9 givenname: Sunit surname: Das fullname: Das, Sunit organization: Division of Neurosurgery and Centre for Ethics, St. Michael’s Hospital, Toronto, Canada – sequence: 10 givenname: Pejman Jabehdar surname: Maralani fullname: Maralani, Pejman Jabehdar organization: Department of Medical Imaging, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada – sequence: 11 givenname: Nir surname: Lipsman fullname: Lipsman, Nir organization: Division of Neurosurgery, University of Toronto, Toronto, Canada – sequence: 12 givenname: Greg surname: Stanisz fullname: Stanisz, Greg organization: Department of Physical Sciences, Sunnybrook Research Institute, Toronto, Canada – sequence: 13 givenname: James surname: Perry fullname: Perry, James organization: Division of Neurology, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada – sequence: 14 givenname: Hanbo surname: Chen fullname: Chen, Hanbo organization: Department of Radiation Oncology, Sunnybrook Odette Cancer Centre, Toronto, Canada – sequence: 15 givenname: Eshetu G. surname: Atenafu fullname: Atenafu, Eshetu G. organization: Department of Biostatistics, University Health Network, University of Toronto, Toronto, Canada – sequence: 16 givenname: Mikki surname: Campbell fullname: Campbell, Mikki organization: Department of Radiation Oncology, Sunnybrook Odette Cancer Centre, Toronto, Canada – sequence: 17 givenname: Angus Z. surname: Lau fullname: Lau, Angus Z. organization: Department of Physical Sciences, Sunnybrook Research Institute, Toronto, Canada – sequence: 18 givenname: Mark surname: Ruschin fullname: Ruschin, Mark organization: Department of Radiation Oncology, University of Toronto, Toronto, Canada – sequence: 19 givenname: Sten surname: Myrehaug fullname: Myrehaug, Sten email: sten.myrehaug@sunnybrook.ca organization: Department of Radiation Oncology, Sunnybrook Odette Cancer Centre, Toronto, Canada |
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Title | Quantitating Interfraction Target Dynamics During Concurrent Chemoradiation for Glioblastoma: A Prospective Serial Imaging Study |
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