ArticleNeuroradiology2026
Incidence and time course of new contrast-enhancing lesions on MRI after proton versus photon radiotherapy in glioma patients.
Article in Neuroradiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Efficacy and safety of proton radiotherapy for progressive or surgically unfavorable adult pilocytic astrocytoma: a single-center experience.Journal of neuro-oncology · 2026Article
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11 authors.
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Abstract
purposeOur aim was to evaluate the incidence and time course of new contrast-enhancing lesions (CEL) after high-dose irradiation therapy (RT) with protons or photons in adult glioma patients.
methodsWe retrospectively analyzed the MRI data sets of 240 consecutive, adult patients with gliomas who received high-dose photon (n = 141) or proton (n = 99) therapy. All available follow-up MRIs were analyzed for incidence of any new CELs. Postradiogenic contrast-enhancing lesions (pCEL) were distinguished from tumor progression either histologically (definite pCEL) or based on follow-up imaging demonstrating spontaneous complete or partial regression (probable pCEL).
resultsDuring a median follow-up period of 30 months, we observed any new CEL in 74.2% of patients. Of these, 53.9% met the criteria for definite or probable tumor progression, while 28.8% met the criteria for definite or probable pCEL. The incidence of pCEL was significantly higher after proton therapy (47.5%, n = 47 of 99 patients) versus photon therapy (15.6%, n = 22 of 141 patients, p < 0.0001). The median time interval between end of RT and first evidence of pCEL was significantly shorter after proton therapy (11.4 months) compared to photon therapy (16.5 months, p = 0.035).
conclusionPostradiogenic CELs are a frequent finding in adult patients with gliomas, particularly in those treated with proton therapy. Awareness of the high incidence, variable morphology and time course of these treatment related changes is essential for correct interpretation of follow-up imaging findings and for appropriate patient management.
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