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Independent validation of a new reirradiation risk score (RRRS) for glioma patients predicting post-recurrence survival: A multicenter DKTK/ROG analysis.
Niyazi, Maximilian; Adeberg, Sebastian; Kaul, David; Boulesteix, Anne-Laure; Bougatf, Nina; Fleischmann, Daniel F; Grün, Arne; Krämer, Anna; Rödel, Claus; Eckert, Franziska; Paulsen, Frank; Kessel, Kerstin A; Combs, Stephanie E; Oehlke, Oliver; Grosu, Anca-Ligia; Seidlitz, Annekatrin; Lattermann, Annika; Krause, Mechthild; Baumann, Michael; Guberina, Maja; Stuschke, Martin; Budach, Volker; Belka, Claus; Debus, Jürgen.
  • Niyazi M; Department of Radiation Oncology, University Hospital, LMU Munich, Germany; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany. Electronic address: maximilian.niyazi@m
  • Adeberg S; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, University of Heidelberg, Germany; Heidelberg Institute for Radiation Oncology (H
  • Kaul D; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, Charité-University Hospital Berlin, Germany.
  • Boulesteix AL; Institute for Medical Information Processing, Biometry and Epidemiology, University of Munich, Germany.
  • Bougatf N; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, University of Heidelberg, Germany; Heidelberg Institute for Radiation Oncology (H
  • Fleischmann DF; Department of Radiation Oncology, University Hospital, LMU Munich, Germany; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Grün A; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, Charité-University Hospital Berlin, Germany.
  • Krämer A; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, University Hospital Johann Wolfgang Goethe University, Frankfurt, Germany.
  • Rödel C; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, University Hospital Johann Wolfgang Goethe University, Frankfurt, Germany.
  • Eckert F; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, University Hospital Johann Wolfgang Goethe University, Frankfurt, Germany.
  • Paulsen F; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, Faculty of Medicine and University Hospital Tübingen, Eberhard Karls University T
  • Kessel KA; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, Klinikum rechts der Isar, Technische Universität München, Germany.
  • Combs SE; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, Klinikum rechts der Isar, Technische Universität München, Germany.
  • Oehlke O; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, University Medical Center Freiburg, Germany.
  • Grosu AL; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, University Medical Center Freiburg, Germany.
  • Seidlitz A; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiotherapy and Radiation Oncology, Faculty of Medicine and University Hospital Carl Gustav Carus, T
  • Lattermann A; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiotherapy and Radiation Oncology, Faculty of Medicine and University Hospital Carl Gustav Carus, T
  • Krause M; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiotherapy and Radiation Oncology, Faculty of Medicine and University Hospital Carl Gustav Carus, T
  • Baumann M; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiotherapy and Radiation Oncology, Faculty of Medicine and University Hospital Carl Gustav Carus, T
  • Guberina M; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiotherapy, University of Duisburg-Essen, University Hospital Essen, Germany.
  • Stuschke M; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiotherapy, University of Duisburg-Essen, University Hospital Essen, Germany.
  • Budach V; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, Charité-University Hospital Berlin, Germany.
  • Belka C; Department of Radiation Oncology, University Hospital, LMU Munich, Germany; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Debus J; German Cancer Consortium (DKTK), partner sites Munich, Heidelberg, Berlin, Frankfurt, Tübingen, Freiburg, Dresden, Essen; and German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Radiation Oncology, Heidelberg Ion Therapy Center (HIT), Heidelberg Institute of Radiation Oncology (
Radiother Oncol ; 127(1): 121-127, 2018 04.
Article en En | MEDLINE | ID: mdl-29433917
ABSTRACT
BACKGROUND AND

PURPOSE:

Reirradiation (reRT) is a valid option with considerable efficacy in patients with recurrent high-grade glioma, but it is still not known which patients might be optimal candidates for a second course of irradiation. This study validated a newly developed prognostic score independently in an external patient cohort. MATERIAL AND

METHODS:

The reRT risk score (RRRS) is based on a linear combination of initial histology, clinical performance status, and age derived from a multivariable model of 353 patients. This score can predict post-recurrence survival (PRS) after reRT. The validation dataset consisted of 212 patients.

RESULTS:

The RRRS differentiates three prognostic groups. Discrimination and calibration were maintained in the validation group. Median PRS times in the development cohort for the good/intermediate/poor risk categories were 14.2, 9.1, and 5.3 months, respectively. The respective groups within the validation cohort displayed median PRS times of 13.8, 8.8, and 3.8 months, respectively. Uno's C for development data was 0.64 (CI 0.60-0.69) and for validation data 0.63 (CI 0.58-0.68).

CONCLUSIONS:

The RRRS has been successfully validated in an independent patient cohort. This linear combination of three easily determined clinicopathological factors allows for a reliable classification of patients and may be used as stratification factor for future trials.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Reirradiación / Glioma / Recurrencia Local de Neoplasia Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País como asunto: Europa Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Reirradiación / Glioma / Recurrencia Local de Neoplasia Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País como asunto: Europa Idioma: En Año: 2018 Tipo del documento: Article