Pre- and Posttherapy Risk Factors for Vasculopathy in Pediatric Patients With Craniopharyngioma Treated With Surgery and Proton Radiation Therapy
Vasculopathy (VAS) is a significant complication associated with radiation therapy in patients treated for brain tumors. We studied the type, location, severity, timing, and resolution of VAS in children with craniopharyngioma treated with proton radiation therapy (PRT) and evaluated predictors of s...
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| Veröffentlicht in: | International journal of radiation oncology, biology, physics Jg. 113; H. 1; S. 152 |
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01.05.2022
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| Abstract | Vasculopathy (VAS) is a significant complication associated with radiation therapy in patients treated for brain tumors. We studied the type, location, severity, timing, and resolution of VAS in children with craniopharyngioma treated with proton radiation therapy (PRT) and evaluated predictors of stenosis (STN) using a novel patient and imaging-based modeling approach.
Children with craniopharyngioma (n = 94) were treated with 54 Gy relative biological effectiveness PRT in a clinical trial, NCT01419067. We evaluated VAS type, location, severity, and resolution. VAS events were segmented and related to their location, operative corridor, PRT dose, and vascular territory to facilitate mixed effect logistic regression modeling of spatial predictors of STN events.
Forty-five (47.9%) patients had 111 instances of confirmed VAS (pre-PRT n = 37, 33.3%). The median time to post-PRT VAS was 3.41 years (95% confidence interval, 1.86-6.11). STN events were observed post-PRT in 23.4% (n = 22) of patients. Post-PRT VAS was detected by cerebral angiogram in 9.6% (n = 9), severe in 4.3% (n = 4), and compensated on perfusion in 2.1% (n = 2). Revascularization was required for 5 (5.3%) patients. Postsurgical, pre-PRT VAS, and PRT dose to unperturbed vessels were predictive of STN. The effect of PRT on STN was negligible within the surgical corridor.
VAS often precedes PRT and was the strongest predictor of post-PRT STN. The adverse effect of PRT on STN was only apparent in unperturbed vasculature beyond the operative corridor. |
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| AbstractList | Vasculopathy (VAS) is a significant complication associated with radiation therapy in patients treated for brain tumors. We studied the type, location, severity, timing, and resolution of VAS in children with craniopharyngioma treated with proton radiation therapy (PRT) and evaluated predictors of stenosis (STN) using a novel patient and imaging-based modeling approach.PURPOSEVasculopathy (VAS) is a significant complication associated with radiation therapy in patients treated for brain tumors. We studied the type, location, severity, timing, and resolution of VAS in children with craniopharyngioma treated with proton radiation therapy (PRT) and evaluated predictors of stenosis (STN) using a novel patient and imaging-based modeling approach.Children with craniopharyngioma (n = 94) were treated with 54 Gy relative biological effectiveness PRT in a clinical trial, NCT01419067. We evaluated VAS type, location, severity, and resolution. VAS events were segmented and related to their location, operative corridor, PRT dose, and vascular territory to facilitate mixed effect logistic regression modeling of spatial predictors of STN events.METHODS AND MATERIALSChildren with craniopharyngioma (n = 94) were treated with 54 Gy relative biological effectiveness PRT in a clinical trial, NCT01419067. We evaluated VAS type, location, severity, and resolution. VAS events were segmented and related to their location, operative corridor, PRT dose, and vascular territory to facilitate mixed effect logistic regression modeling of spatial predictors of STN events.Forty-five (47.9%) patients had 111 instances of confirmed VAS (pre-PRT n = 37, 33.3%). The median time to post-PRT VAS was 3.41 years (95% confidence interval, 1.86-6.11). STN events were observed post-PRT in 23.4% (n = 22) of patients. Post-PRT VAS was detected by cerebral angiogram in 9.6% (n = 9), severe in 4.3% (n = 4), and compensated on perfusion in 2.1% (n = 2). Revascularization was required for 5 (5.3%) patients. Postsurgical, pre-PRT VAS, and PRT dose to unperturbed vessels were predictive of STN. The effect of PRT on STN was negligible within the surgical corridor.RESULTSForty-five (47.9%) patients had 111 instances of confirmed VAS (pre-PRT n = 37, 33.3%). The median time to post-PRT VAS was 3.41 years (95% confidence interval, 1.86-6.11). STN events were observed post-PRT in 23.4% (n = 22) of patients. Post-PRT VAS was detected by cerebral angiogram in 9.6% (n = 9), severe in 4.3% (n = 4), and compensated on perfusion in 2.1% (n = 2). Revascularization was required for 5 (5.3%) patients. Postsurgical, pre-PRT VAS, and PRT dose to unperturbed vessels were predictive of STN. The effect of PRT on STN was negligible within the surgical corridor.VAS often precedes PRT and was the strongest predictor of post-PRT STN. The adverse effect of PRT on STN was only apparent in unperturbed vasculature beyond the operative corridor.CONCLUSIONSVAS often precedes PRT and was the strongest predictor of post-PRT STN. The adverse effect of PRT on STN was only apparent in unperturbed vasculature beyond the operative corridor. Vasculopathy (VAS) is a significant complication associated with radiation therapy in patients treated for brain tumors. We studied the type, location, severity, timing, and resolution of VAS in children with craniopharyngioma treated with proton radiation therapy (PRT) and evaluated predictors of stenosis (STN) using a novel patient and imaging-based modeling approach. Children with craniopharyngioma (n = 94) were treated with 54 Gy relative biological effectiveness PRT in a clinical trial, NCT01419067. We evaluated VAS type, location, severity, and resolution. VAS events were segmented and related to their location, operative corridor, PRT dose, and vascular territory to facilitate mixed effect logistic regression modeling of spatial predictors of STN events. Forty-five (47.9%) patients had 111 instances of confirmed VAS (pre-PRT n = 37, 33.3%). The median time to post-PRT VAS was 3.41 years (95% confidence interval, 1.86-6.11). STN events were observed post-PRT in 23.4% (n = 22) of patients. Post-PRT VAS was detected by cerebral angiogram in 9.6% (n = 9), severe in 4.3% (n = 4), and compensated on perfusion in 2.1% (n = 2). Revascularization was required for 5 (5.3%) patients. Postsurgical, pre-PRT VAS, and PRT dose to unperturbed vessels were predictive of STN. The effect of PRT on STN was negligible within the surgical corridor. VAS often precedes PRT and was the strongest predictor of post-PRT STN. The adverse effect of PRT on STN was only apparent in unperturbed vasculature beyond the operative corridor. |
| Author | Boop, Fredrick A Li, Yimei Lucas, Jr, John T Ismael, Yousef Darrow, Kaleb Moskvin, Vadim P Indelicato, Daniel J Guo, Yian Khan, Raja Wilson, Lydia J LeVine, David A Pirlepesov, Fakhriddin Elijovich, Lucas Becksfort, Jared B Klimo, Paul Merchant, Thomas E Faught, Austin M Hsu, Chih Yang |
| Author_xml | – sequence: 1 givenname: John T surname: Lucas, Jr fullname: Lucas, Jr, John T email: john.lucas@stjude.org organization: Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee. Electronic address: john.lucas@stjude.org – sequence: 2 givenname: Austin M surname: Faught fullname: Faught, Austin M organization: Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee – sequence: 3 givenname: Chih Yang surname: Hsu fullname: Hsu, Chih Yang organization: GlaxoSmithKline, Exton, Pennsylvania – sequence: 4 givenname: Lydia J surname: Wilson fullname: Wilson, Lydia J organization: Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee – sequence: 5 givenname: Yian surname: Guo fullname: Guo, Yian organization: Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee – sequence: 6 givenname: Yimei surname: Li fullname: Li, Yimei organization: Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee – sequence: 7 givenname: Raja surname: Khan fullname: Khan, Raja organization: Department of Neurology, St. Jude Children's Research Hospital, Memphis, Tennessee – sequence: 8 givenname: Jared B surname: Becksfort fullname: Becksfort, Jared B organization: Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee – sequence: 9 givenname: David A surname: LeVine fullname: LeVine, David A organization: University of Tennessee Health Sciences Center, Memphis, Tennessee – sequence: 10 givenname: Yousef surname: Ismael fullname: Ismael, Yousef organization: Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee – sequence: 11 givenname: Kaleb surname: Darrow fullname: Darrow, Kaleb organization: University of Tennessee Health Sciences Center, Memphis, Tennessee – sequence: 12 givenname: Vadim P surname: Moskvin fullname: Moskvin, Vadim P organization: Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee – sequence: 13 givenname: Fakhriddin surname: Pirlepesov fullname: Pirlepesov, Fakhriddin organization: Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee – sequence: 14 givenname: Paul surname: Klimo fullname: Klimo, Paul organization: Semmes Murphey Neurologic & Spine Institute, Memphis, Tennessee; Department of Neurosurgery, University of Tennessee Health Science Center, Memphis, Tennessee – sequence: 15 givenname: Lucas surname: Elijovich fullname: Elijovich, Lucas organization: Department of Neurology, University of Tennessee Health Sciences Center, Memphis, Tennessee; Semmes Murphey Neurologic & Spine Institute, Memphis, Tennessee; Department of Neurosurgery, University of Tennessee Health Science Center, Memphis, Tennessee – sequence: 16 givenname: Daniel J surname: Indelicato fullname: Indelicato, Daniel J organization: Department of Radiation Oncology, University of Florida, Jacksonville, Florida – sequence: 17 givenname: Fredrick A surname: Boop fullname: Boop, Fredrick A organization: Semmes Murphey Neurologic & Spine Institute, Memphis, Tennessee; Department of Neurosurgery, University of Tennessee Health Science Center, Memphis, Tennessee – sequence: 18 givenname: Thomas E surname: Merchant fullname: Merchant, Thomas E organization: Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee |
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| Snippet | Vasculopathy (VAS) is a significant complication associated with radiation therapy in patients treated for brain tumors. We studied the type, location,... |
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| SubjectTerms | Child Craniopharyngioma - radiotherapy Craniopharyngioma - surgery Humans Pituitary Neoplasms - radiotherapy Pituitary Neoplasms - surgery Proton Therapy - adverse effects Proton Therapy - methods Protons Risk Factors |
| Title | Pre- and Posttherapy Risk Factors for Vasculopathy in Pediatric Patients With Craniopharyngioma Treated With Surgery and Proton Radiation Therapy |
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