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Undetected pseudoprogressions in the CeTeG/NOA-09 trial: hints from postprogression survival and MRI analyses.
Zeyen, Thomas; Paech, Daniel; Weller, Johannes; Schäfer, Niklas; Tzaridis, Theophilos; Duffy, Cathrina; Nitsch, Louisa; Schneider, Matthias; Potthoff, Anna-Laura; Steinbach, Joachim Peter; Hau, Peter; Schlegel, Uwe; Seidel, Clemens; Krex, Dietmar; Grauer, Oliver; Goldbrunner, Roland; Zeiner, Pia Susan; Tabatabai, Ghazaleh; Galldiks, Norbert; Stummer, Walter; Hattingen, Elke; Glas, Martin; Radbruch, Alexander; Herrlinger, Ulrich; Schaub, Christina.
Afiliación
  • Zeyen T; Division of Clinical Neurooncology, Department of Neurology, University Hospital Bonn, Bonn, Germany.
  • Paech D; Department of Neuroradiology, University Hospital Bonn, Bonn, Germany.
  • Weller J; Division of Clinical Neurooncology, Department of Neurology, University Hospital Bonn, Bonn, Germany.
  • Schäfer N; Division of Clinical Neurooncology, Department of Neurology, University Hospital Bonn, Bonn, Germany.
  • Tzaridis T; Division of Clinical Neurooncology, Department of Neurology, University Hospital Bonn, Bonn, Germany.
  • Duffy C; Division of Clinical Neurooncology, Department of Neurology, University Hospital Bonn, Bonn, Germany.
  • Nitsch L; Division of Clinical Neurooncology, Department of Neurology, University Hospital Bonn, Bonn, Germany.
  • Schneider M; Department of Neurosurgery, University Hospital Bonn, Bonn, Germany.
  • Potthoff AL; Department of Neurosurgery, University Hospital Bonn, Bonn, Germany.
  • Steinbach JP; Dr. Senckenberg Institute of Neurooncology, University of Frankfurt, Frankfurt, Germany.
  • Hau P; Department of Neurology and Wilhelm Sander NeuroOncology Unit, University Hospital Regensburg, Regensburg, Germany.
  • Schlegel U; Department of Neurology, Klinik Hirslanden, Zürich, Switzerland.
  • Seidel C; Department of Radiation Oncology, University of Leipzig, Leipzig, Germany.
  • Krex D; Department of Neurosurgery, Technische Universität Dresden, Faculty of Medicine and University Hospital Carl Gustav Carus, Fetscherstrasse 74, 01307, Dresden, Germany.
  • Grauer O; Department of Neurology, University of Münster, Münster, Germany.
  • Goldbrunner R; Center of Neurosurgery Department of General, Neurosurgery University of Cologne, Cologne, Germany.
  • Zeiner PS; Dr. Senckenberg Institute of Neurooncology, University of Frankfurt, Frankfurt, Germany.
  • Tabatabai G; Department of Neurology and Interdisciplinary Neuro-Oncology, Institute for Clinical Brain Research, University Hospital Tübingen, Eberhard Karls University Tübingen, HertieTübingen, Germany.
  • Galldiks N; Center for Neuro-Oncology, Comprehensive Cancer Center Tübingen-Stuttgart, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany.
  • Stummer W; Department of Neurology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany and Research Center Juelich, Inst. of Neuroscience and Medicine (INM-3), Juelich, Germany.
  • Hattingen E; Department of Neurosurgery, University of Münster, Münster, Germany.
  • Glas M; Department of Neuroradiology, University Hospital Frankfurt, 60590, Frankfurt Am Main, Germany.
  • Radbruch A; Division of Clinical Neurooncology, Department of Neurology and Center for Translational Neuro- and Behavioral Sciences (C-TNBS), University Medicine Essen, University Duisburg-Essen, Essen, Germany.
  • Herrlinger U; German Cancer Consortium (DKTK), Partner Site University Medicine Essen, Hufelandstr. 55, 45147, Essen, Germany.
  • Schaub C; Department of Neuroradiology, University Hospital Bonn, Bonn, Germany.
J Neurooncol ; 164(3): 607-616, 2023 Sep.
Article en En | MEDLINE | ID: mdl-37728779
ABSTRACT

PURPOSE:

In the randomized CeTeG/NOA-09 trial, lomustine/temozolomide (CCNU/TMZ) was superior to TMZ therapy regarding overall survival (OS) in MGMT promotor-methylated glioblastoma. Progression-free survival (PFS) and pseudoprogression rates (about 10%) were similar in both arms. Further evaluating this discrepancy, we analyzed patterns of postprogression survival (PPS) and MRI features at first progression according to modified RANO criteria (mRANO).

METHODS:

We classified the patients of the CeTeG/NOA-09 trial according to long vs. short PPS employing a cut-off of 18 months and compared baseline characteristics and survival times. In patients with available MRIs and confirmed progression, the increase in T1-enhancing, FLAIR hyperintense lesion volume and the change in ADC mean value of contrast-enhancing tumor upon progression were determined.

RESULTS:

Patients with long PPS in the CCNU/TMZ arm had a particularly short PFS (5.6 months). PFS in this subgroup was shorter than in the long PPS subgroup of the TMZ arm (11.1 months, p = 0.01). At mRANO-defined progression, patients of the CCNU/TMZ long PPS subgroup had a significantly higher increase of mean ADC values (p = 0.015) and a tendency to a stronger volumetric increase in T1-enhancement (p = 0.22) as compared to long PPS patients of the TMZ arm.

CONCLUSION:

The combination of survival and MRI analyses identified a subgroup of CCNU/TMZ-treated patients with features that sets them apart from other patients in the trial short first PFS despite long PPS and significant increase in mean ADC values upon mRANO-defined progression. The observed pattern is compatible with the features commonly observed in pseudoprogression suggesting mRANO-undetected pseudoprogressions in the CCNU/TMZ arm of CeTeG/NOA-09.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: J Neurooncol Año: 2023 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: J Neurooncol Año: 2023 Tipo del documento: Article País de afiliación: Alemania