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Eur J Neurol ; 20(10): 1335-41, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23679051

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.


Subject(s)
Brain Neoplasms/pathology , Brain/pathology , DNA Modification Methylases/genetics , DNA Repair Enzymes/genetics , Glioblastoma/pathology , Radiation Injuries/diagnosis , Tumor Suppressor Proteins/genetics , Adolescent , Adult , Aged , Aged, 80 and over , Antineoplastic Agents/administration & dosage , Brain Neoplasms/mortality , Brain Neoplasms/therapy , Chemoradiotherapy , DNA Methylation , Dacarbazine/administration & dosage , Dacarbazine/analogs & derivatives , Female , Glioblastoma/mortality , Glioblastoma/therapy , Humans , Incidence , Kaplan-Meier Estimate , Male , Middle Aged , Promoter Regions, Genetic/genetics , Radiation Injuries/epidemiology , Retrospective Studies , Risk Factors , Temozolomide , Young Adult
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