Background: Pseudoprogression (PsP) following radiation therapy (RT) for low grade glioma (LGG, WHO grade I and II), including both photon-based intensity-modulated RT (IMRT) and proton beam therapy (PBT), has been described. However, its incidence has yet to be consolidated. The aim of this systematic review and meta-analysis was to pool the current literature and establish the incidence of PsP in these groups to better inform surveillance protocols in the future. Methods: Searches of 4 electronic databases from inception to April 2019 were conducted following PRISMA guidelines. Articles were screened against pre-specified criteria. The incidence of outcomes was then extracted and pooled by random-effects meta-analysis of proportions. Results: A total of 5 pediatric and 4 adult cohort studies describing 517 and 424 LGG subjects respectively satisfied all selection criteria. The estimated incidences of PsP in pediatric subjects following IMRT and PBT were 33% (95% CI, 20-47%) and 34% (95% CI, 23-45%) respectively, with no difference between modalities. The estimated incidences of PsP in adult subjects following IMRT and PBT were 18% (95% CI, 12-25%) and 30% (95% CI, 21-39%) respectively, with PsP significantly less common following IMRT than PBT (P-heterogeneity = 0.04). Median time from radiation initiation to first detection of PsP ranged from 6 to 12 months across all modalities and age groups. Conclusions: The incidence of PsP following both IMRT and PBT in the management of pediatric and adult LGG is not negligible, and should therefore be recognized as a pertinent sequala within the first year at least following treatment. However, a lack of accountability in the current literature for the differences in PsP interpretation, radiation modality, radiobiology and molecular biology of LGGs precludes any firm surveillance recommendations at this time. (C) 2019 Elsevier B.V. All rights reserved.
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Univ Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USAUniv Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA
Brown, Timothy J.
Bota, Daniela A.
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Univ Calif Irvine, Dept Neurol, Irvine, CA 92717 USA
Univ Calif Irvine, Dept Neurol Surg, Irvine, CA 92717 USA
Penn State Milton S Hershey Med Ctr, Dept Neurosurg, Hershey, PA USA
Penn State Milton S Hershey Med Ctr, Dept Oncol, Hershey, PA USAUniv Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA
Bota, Daniela A.
van den Bent, Martin J.
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Erasmus MC Canc Ctr, Dept Neurol, Rotterdam, NetherlandsUniv Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA
van den Bent, Martin J.
Brown, Paul D.
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Mayo Clin, Dept Radiat Oncol, Rochester, MN USAUniv Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA
Brown, Paul D.
Maher, Elizabeth
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Univ Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USAUniv Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA
Maher, Elizabeth
Aregawi, Dawit
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机构:Univ Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA
Aregawi, Dawit
Liau, Linda M.
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Univ Calif Los Angeles, Dept Neurol Surg, Los Angeles, CA 90024 USAUniv Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA
Liau, Linda M.
Buckner, Jan C.
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Mayo Clin, Dept Oncol, Rochester, MN USAUniv Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA
Buckner, Jan C.
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Weller, Michael
Berger, Mitchel S.
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Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USAUniv Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA
Berger, Mitchel S.
Glantz, Michael
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Penn State Milton S Hershey Med Ctr, Dept Neurosurg, Hershey, PA USA
Penn State Milton S Hershey Med Ctr, Dept Oncol, Hershey, PA USAUniv Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA