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Early treatment response evaluation using FET PET compared to MRI in glioblastoma patients at first progression treated with bevacizumab plus lomustine.
Galldiks, Norbert; Dunkl, Veronika; Ceccon, Garry; Tscherpel, Caroline; Stoffels, Gabriele; Law, Ian; Henriksen, Otto M; Muhic, Aida; Poulsen, Hans S; Steger, Jan; Bauer, Elena K; Lohmann, Philipp; Schmidt, Matthias; Shah, Nadim J; Fink, Gereon R; Langen, Karl-Josef.
Afiliación
  • Galldiks N; Department of Neurology, University Hospital Cologne, Josef-Stelzmann St. 9, 50937, Cologne, Germany. n.galldiks@fz-juelich.de.
  • Dunkl V; Institute of Neuroscience and Medicine (INM-3, -4), Forschungszentrum Juelich, Leo-Brandt-St. 5, 52425, Juelich, Germany. n.galldiks@fz-juelich.de.
  • Ceccon G; Center of Integrated Oncology (CIO), Universities of Cologne and Bonn, Cologne, Germany. n.galldiks@fz-juelich.de.
  • Tscherpel C; Department of Neurology, University Hospital Cologne, Josef-Stelzmann St. 9, 50937, Cologne, Germany.
  • Stoffels G; Department of Neurology, University Hospital Cologne, Josef-Stelzmann St. 9, 50937, Cologne, Germany.
  • Law I; Department of Neurology, University Hospital Cologne, Josef-Stelzmann St. 9, 50937, Cologne, Germany.
  • Henriksen OM; Institute of Neuroscience and Medicine (INM-3, -4), Forschungszentrum Juelich, Leo-Brandt-St. 5, 52425, Juelich, Germany.
  • Muhic A; Institute of Neuroscience and Medicine (INM-3, -4), Forschungszentrum Juelich, Leo-Brandt-St. 5, 52425, Juelich, Germany.
  • Poulsen HS; Department of Clinical Physiology, Nuclear Medicine & PET, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Steger J; Department of Clinical Physiology, Nuclear Medicine & PET, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Bauer EK; Department of Oncology, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Lohmann P; Department of Oncology, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Schmidt M; Department of Neurology, University Hospital Cologne, Josef-Stelzmann St. 9, 50937, Cologne, Germany.
  • Shah NJ; Department of Neurology, University Hospital Cologne, Josef-Stelzmann St. 9, 50937, Cologne, Germany.
  • Fink GR; Institute of Neuroscience and Medicine (INM-3, -4), Forschungszentrum Juelich, Leo-Brandt-St. 5, 52425, Juelich, Germany.
  • Langen KJ; Dept. of Nuclear Medicine, University Hospital Cologne, Cologne, Germany.
Eur J Nucl Med Mol Imaging ; 45(13): 2377-2386, 2018 12.
Article en En | MEDLINE | ID: mdl-29982845
ABSTRACT

BACKGROUND:

The goal of this prospective study was to compare the value of both conventional MRI and O-(2-18F-fluoroethyl)-L-tyrosine (FET) PET for response evaluation in glioblastoma patients treated with bevacizumab plus lomustine (BEV/LOM) at first progression.

METHODS:

After chemoradiation with concomitant and adjuvant temozolomide, 21 IDH wild-type glioblastoma patients at first progression (age range, 33-75 years; MGMT promoter unmethylated, 81%) were treated with BEV/LOM. Contrast-enhanced MRI and FET-PET scans were performed at baseline and after 8-10 weeks. We obtained FET metabolic tumor volumes (MTV) and tumor/brain ratios. Threshold values of FET-PET parameters for treatment response were established by ROC analyses using the post-progression overall survival (OS) ≤/>9 months as the reference. MRI response assessment was based on RANO criteria. The predictive ability of FET-PET thresholds and MRI changes on early response assessment was evaluated subsequently concerning OS using uni- and multivariate survival estimates.

RESULTS:

Early treatment response as assessed by RANO criteria was not predictive for an OS>9 months (P = 0.203), whereas relative reductions of all FET-PET parameters significantly predicted an OS>9 months (P < 0.05). The absolute MTV at follow-up enabled the most significant OS prediction (sensitivity, 85%; specificity, 88%; P = 0.001). Patients with an absolute MTV below 5 ml at follow-up survived significantly longer (12 vs. 6 months, P < 0.001), whereas early responders defined by RANO criteria lived only insignificantly longer (9 vs. 6 months; P = 0.072). The absolute MTV at follow-up remained significant in the multivariate survival analysis (P = 0.006).

CONCLUSIONS:

FET-PET appears to be useful for identifying responders to BEV/LOM early after treatment initiation.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Tirosina / Imagen por Resonancia Magnética / Glioblastoma / Tomografía de Emisión de Positrones / Bevacizumab / Lomustina Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Nucl Med Mol Imaging Asunto de la revista: MEDICINA NUCLEAR Año: 2018 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Asunto principal: Tirosina / Imagen por Resonancia Magnética / Glioblastoma / Tomografía de Emisión de Positrones / Bevacizumab / Lomustina Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Nucl Med Mol Imaging Asunto de la revista: MEDICINA NUCLEAR Año: 2018 Tipo del documento: Article País de afiliación: Alemania