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Diagnostic impact of additional O-(2-[18F]fluoroethyl)-L-tyrosine (18F-FET) PET following immunotherapy with dendritic cell vaccination in glioblastoma patients.
Kristin Schmitz, Ann; Sorg, Rüdiger V; Stoffels, Gabriele; Grauer, Oliver M; Galldiks, Norbert; Steiger, Hans-Jakob; Kamp, Marcel A; Langen, Karl-Josef; Sabel, Michael; Rapp, Marion.
Afiliación
  • Kristin Schmitz A; Department of Neurosurgery, Faculty of Medicine, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
  • Sorg RV; Institute for Transplantation Diagnostics and Cell Therapeutics, Faculty of Medicine, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
  • Stoffels G; Institute of Neuroscience and Medicine, Research Center Jülich, Jülich, Germany.
  • Grauer OM; Department of Neurology, Faculty of Medicine, Westfälische Wilhelms-University Münster, Münster, Germany.
  • Galldiks N; Institute of Neuroscience and Medicine, Research Center Jülich, Jülich, Germany.
  • Steiger HJ; Department of Neurology, Faculty of Medicine, University of Cologne, Cologne, Germany.
  • Kamp MA; Department of Neurosurgery, Faculty of Medicine, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
  • Langen KJ; Department of Neurosurgery, Faculty of Medicine, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
  • Sabel M; Department of Neurology, Faculty of Medicine, Westfälische Wilhelms-University Münster, Münster, Germany.
  • Rapp M; Department of Neurosurgery, Faculty of Medicine, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Br J Neurosurg ; 35(6): 736-742, 2021 Dec.
Article en En | MEDLINE | ID: mdl-31407920
ABSTRACT

OBJECTIVE:

Vaccination therapy using tumour antigen-loaded, autologous dendritic cells (DC) is a promising therapeutic approach alongside standard treatment for glioblastoma (GBM). However, reliable diagnostic criteria regarding therapy monitoring are not established. Here, we analysed the impact of additional 18F-fluoroethyl-tyrosine positron emission tomography (18F-FET PET) imaging following DC vaccination therapy.

METHODS:

We analysed data of GBM patients who received DC vaccination therapy. Following MRI diagnosis of tumour recurrence, additional static and dynamic 18F-FET PET imaging was performed. Vaccination was performed five times by intradermal injections, either weekly between concomitant radio/-chemotherapy and intermittent chemotherapy or after tumour recurrence, before re-radiation therapy. MRI and 18F-FET PET results were compared and correlated with clinical data.

RESULTS:

Between 2003 and 2016, 5 patients were identified who received DC vaccination and 18F-FET PET imaging (1 female/4 males; mean age 44 ± 14 y). 3/5 patients showed congruent results of tumour progression. In three patients 18F-FET PET indicated treatment related changes, which was in contrast to MRI findings that indicated tumour progression. In these patients 18F-FET PET results could be confirmed by either neuropathological diagnosis or according to the RANO criteria.

CONCLUSIONS:

Despite the small patients number our results indicate an additional impact of 18F-FET PET for monitoring outcome following vaccination therapy.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Neurosurg Asunto de la revista: NEUROCIRURGIA Año: 2021 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Neurosurg Asunto de la revista: NEUROCIRURGIA Año: 2021 Tipo del documento: Article País de afiliación: Alemania