Literature DB >> 23679051

Defining pseudoprogression in glioblastoma multiforme.

E Van Mieghem1, A Wozniak, Y Geussens, J Menten, S De Vleeschouwer, F Van Calenbergh, R Sciot, S Van Gool, O E Bechter, P Demaerel, G Wilms, P M Clement.   

Abstract

BACKGROUND AND
PURPOSE: Pseudoprogression is a frequent phenomenon observed since the introduction of postoperative therapy with radiotherapy and temozolomide (RT/TMZ) in glioblastoma multiforme (GBM) patients. However, the criteria defining pseudoprogression, its incidence, the time of occurrence and its impact on therapy and outcome remain poorly defined.
METHODS: The objective of this study is to compare two sets of criteria (liberal and stringent), defining pseudoprogression, in a cohort of patients treated before and after the introduction of RT/TMZ in the standard postoperative treatment. This retrospective review includes 136 unselected and consecutively treated patients with pathologically diagnosed GBM.
RESULTS: Pseudoprogression was observed in 10 (12%) cases applying the stringent criteria, and in 18 (23%) patients when using the liberal criteria, in the cohort treated with RT/TMZ. Pseudoprogression was observed in only one patient treated with RT alone. The median time to pseudoprogression was 4 weeks after the end of RT. Patients with pseudoprogression had a median survival time of 28 months, compared with 12 months for patients without pseudoprogression.
CONCLUSIONS: The incidence of pseudoprogression after RT/TMZ strongly depends on the applied criteria. However, regardless of the stringency of the criteria, the impact on survival remains the same.
© 2013 The Author(s) European Journal of Neurology © 2013 EFNS.

Entities:  

Keywords:  chemotherapy; glioblastoma; pseudoprogression; radiotherapy; temozolomide

Mesh:

Substances:

Year:  2013        PMID: 23679051     DOI: 10.1111/ene.12192

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  21 in total

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Journal:  J Neurooncol       Date:  2017-04-05       Impact factor: 4.130

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Journal:  Proc Natl Acad Sci U S A       Date:  2015-07-20       Impact factor: 11.205

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7.  Post-chemoradiation volumetric response predicts survival in newly diagnosed glioblastoma treated with radiation, temozolomide, and bevacizumab or placebo.

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8.  Isocitrate dehydrogenase 1 mutant glioblastomas demonstrate a decreased rate of pseudoprogression: a multi-institutional experience.

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9.  Evaluation of pseudoprogression in patients with glioblastoma.

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Review 10.  Emerging Technologies for Non-invasive Monitoring of Treatment Response to Immunotherapy for Brain Tumors.

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