Incidence and outcome of pseudoprogression after radiation therapy in glioblastoma patients: A cohort study.

associated factors chemoradiotherapy glioblastoma prognostic factors pseudoprogression

Journal

Neuro-oncology practice
ISSN: 2054-2577
Titre abrégé: Neurooncol Pract
Pays: England
ID NLM: 101640528

Informations de publication

Date de publication:
Feb 2024
Historique:
medline: 15 1 2024
pubmed: 15 1 2024
entrez: 15 1 2024
Statut: epublish

Résumé

Differentiating post-radiation MRI changes from progressive disease (PD) in glioblastoma (GBM) patients represents a major challenge. The clinical problem is two-sided; avoid termination of effective therapy in case of pseudoprogression (PsP) and continuation of ineffective therapy in case of PD. We retrospectively assessed the incidence, management, and prognostic impact of PsP and analyzed factors associated with PsP in a GBM patient cohort. Consecutive GBM patients diagnosed in the South-Eastern Norway Health Region from 2015 to 2018 who had received RT and follow-up MRI were included. Tumor, patient, and treatment characteristics were analyzed in relationship to re-evaluated MRI examinations at 3 and 6 months post-radiation using Response Assessment in Neuro-Oncology criteria. A total of 284 patients were included in the study. PsP incidence 3 and 6 months post-radiation was 19.4% and 7.0%, respectively. In adjusted analyses, methylated PsP incidence was similar to previous reports. In addition to the previously described correlation of methylated

Sections du résumé

Background UNASSIGNED
Differentiating post-radiation MRI changes from progressive disease (PD) in glioblastoma (GBM) patients represents a major challenge. The clinical problem is two-sided; avoid termination of effective therapy in case of pseudoprogression (PsP) and continuation of ineffective therapy in case of PD. We retrospectively assessed the incidence, management, and prognostic impact of PsP and analyzed factors associated with PsP in a GBM patient cohort.
Methods UNASSIGNED
Consecutive GBM patients diagnosed in the South-Eastern Norway Health Region from 2015 to 2018 who had received RT and follow-up MRI were included. Tumor, patient, and treatment characteristics were analyzed in relationship to re-evaluated MRI examinations at 3 and 6 months post-radiation using Response Assessment in Neuro-Oncology criteria.
Results UNASSIGNED
A total of 284 patients were included in the study. PsP incidence 3 and 6 months post-radiation was 19.4% and 7.0%, respectively. In adjusted analyses, methylated
Conclusions UNASSIGNED
PsP incidence was similar to previous reports. In addition to the previously described correlation of methylated

Identifiants

pubmed: 38222046
doi: 10.1093/nop/npad063
pii: npad063
pmc: PMC10785573
doi:

Types de publication

Journal Article

Langues

eng

Pagination

36-45

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Neuro-Oncology and the European Association of Neuro-Oncology.

Déclaration de conflit d'intérêts

None declared.

Auteurs

Hanne Blakstad (H)

Department of Oncology, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Eduardo Erasmo Mendoza Mireles (EE)

Department of Neurosurgery, Oslo University Hospital, Oslo, Norway.
Vilhelm Magnus Laboratory, Institute for Surgical Research, Oslo University Hospital, Oslo, Norway.

Liv Cathrine Heggebø (LC)

Department of Oncology, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Henriette Magelssen (H)

Department of Oncology, Oslo University Hospital, Oslo, Norway.

Mette Sprauten (M)

Department of Oncology, Oslo University Hospital, Oslo, Norway.

Tom Børge Johannesen (TB)

Department of Oncology, Oslo University Hospital, Oslo, Norway.
Cancer Registry of Norway, Oslo, Norway.

Einar Osland Vik-Mo (EO)

Department of Neurosurgery, Oslo University Hospital, Oslo, Norway.
Vilhelm Magnus Laboratory, Institute for Surgical Research, Oslo University Hospital, Oslo, Norway.

Henning Leske (H)

Department of Pathology, Oslo University Hospital, Oslo.
University of Oslo, Oslo, Norway.

Pitt Niehusmann (P)

Department of Pathology, Oslo University Hospital, Oslo.
Division of Cancer Medicine, Oslo University Hospital, Oslo.

Karoline Skogen (K)

Department of Radiology, Oslo University Hospital, Oslo, Norway.

Eirik Helseth (E)

Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Department of Neurosurgery, Oslo University Hospital, Oslo, Norway.

Kyrre Eeg Emblem (KE)

Department of Physics and Computational Radiology, Division of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway.

Petter Brandal (P)

Department of Oncology, Oslo University Hospital, Oslo, Norway.
Institute for Cancer Genetics and Informatics, Oslo University Hospital, Oslo, Norway.

Classifications MeSH