Impact of time to initiation of radiotherapy on survival after resection of newly diagnosed glioblastoma.


Journal

Radiation oncology (London, England)
ISSN: 1748-717X
Titre abrégé: Radiat Oncol
Pays: England
ID NLM: 101265111

Informations de publication

Date de publication:
29 Apr 2019
Historique:
received: 10 11 2018
accepted: 07 04 2019
entrez: 1 5 2019
pubmed: 1 5 2019
medline: 10 9 2019
Statut: epublish

Résumé

To evaluate the effect of timing of radiotherapy (RT) on survival in patients with newly diagnosed primary glioblastoma (GBM) treated with the same therapeutical protocol. Patients with newly diagnosed primary GBM treated with the same therapeutical scheme between 2010 and 2015 in our institution were retrospectively reviewed. The population was trichotomized based on the time interval from surgery till initiation of RT (< 28 days, 28-33 days, > 33 days). Kaplan-Meier and Cox regression analyses were used to compare progression free survival (PFS) and overall survival (OS) between the groups. The influence of various extensively studied prognostic factors on survival was assessed by multivariate analysis. One-hundred-fifty-one patients met the inclusion criteria. Between the three groups no significant difference in PFS (p = 0.516) or OS (p = 0.902) could be demonstrated. Residual tumor volume (RTV) and midline structures involvement were identified as independent prognostic factors of PFS while age, O-6-Methylguanine Methyltransferase (MGMT) status, Ki67 index, RTV and midline structures involvement represented independent predictors of OS. Patients starting RT after a prolonged delay (> 48 days) exhibited a significantly shorter OS (p = 0.034). Initiation of RT within a timeframe of 48 days is not associated with worsened survival. A prolonged delay (> 48 days) may be associated with worse OS. RT should neither be delayed, nor forced, but should rather start timely, as soon as the patient has recovered from surgery.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
To evaluate the effect of timing of radiotherapy (RT) on survival in patients with newly diagnosed primary glioblastoma (GBM) treated with the same therapeutical protocol.
MATERIALS AND METHODS METHODS
Patients with newly diagnosed primary GBM treated with the same therapeutical scheme between 2010 and 2015 in our institution were retrospectively reviewed. The population was trichotomized based on the time interval from surgery till initiation of RT (< 28 days, 28-33 days, > 33 days). Kaplan-Meier and Cox regression analyses were used to compare progression free survival (PFS) and overall survival (OS) between the groups. The influence of various extensively studied prognostic factors on survival was assessed by multivariate analysis.
RESULTS RESULTS
One-hundred-fifty-one patients met the inclusion criteria. Between the three groups no significant difference in PFS (p = 0.516) or OS (p = 0.902) could be demonstrated. Residual tumor volume (RTV) and midline structures involvement were identified as independent prognostic factors of PFS while age, O-6-Methylguanine Methyltransferase (MGMT) status, Ki67 index, RTV and midline structures involvement represented independent predictors of OS. Patients starting RT after a prolonged delay (> 48 days) exhibited a significantly shorter OS (p = 0.034).
CONCLUSION CONCLUSIONS
Initiation of RT within a timeframe of 48 days is not associated with worsened survival. A prolonged delay (> 48 days) may be associated with worse OS. RT should neither be delayed, nor forced, but should rather start timely, as soon as the patient has recovered from surgery.

Identifiants

pubmed: 31036031
doi: 10.1186/s13014-019-1272-6
pii: 10.1186/s13014-019-1272-6
pmc: PMC6489245
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

73

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Auteurs

Sotirios Katsigiannis (S)

Department of Neurosurgery, University Hospital of Bochum, In der Schornau Str. 23-25, 44892, Bochum, Germany. sotiriskatsigiannis@yahoo.gr.

Boris Krischek (B)

Department of Neurosurgery, University Hospital Cologne, Kerpener Str. 62, 50937, Cologne, Germany.

Stefanie Barleanu (S)

Department of Neurosurgery, University Hospital Cologne, Kerpener Str. 62, 50937, Cologne, Germany.

Stefan Grau (S)

Department of Neurosurgery, University Hospital Cologne, Kerpener Str. 62, 50937, Cologne, Germany.

Norbert Galldiks (N)

Department of Neurology, University Hospital Cologne, Kerpener Str. 62, 50937, Cologne, Germany.
Institute of Neuroscience and Medicine, Research Center Juelich, Juelich, Germany.
Center of Integrated Oncology (CIO), Universities of Cologne and Bonn, Cologne, Germany.

Marco Timmer (M)

Department of Neurosurgery, University Hospital Cologne, Kerpener Str. 62, 50937, Cologne, Germany.

Christoph Kabbasch (C)

Department of Neuroradiology, University Hospital Cologne, Kerpener Str. 62, 50937, Cologne, Germany.

Roland Goldbrunner (R)

Department of Neurosurgery, University Hospital Cologne, Kerpener Str. 62, 50937, Cologne, Germany.

Pantelis Stavrinou (P)

Department of Neurosurgery, University Hospital Cologne, Kerpener Str. 62, 50937, Cologne, Germany.

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Classifications MeSH