Increasing use of immunotherapy and prolonged survival among younger patients with primary CNS lymphoma: a population-based study

Authors

  • Magdalena Neuhauser Institute of Neurology, Medical University of Vienna, Vienna, Austria; ;Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria
  • Thomas Roetzer Institute of Neurology, Medical University of Vienna, Vienna, Austria; ;Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria
  • Stefan Oberndorfer Department of Neurology, University Hospital St. Poelten, Karl Landsteiner University of Health Sciences, St. Poelten, Austria
  • Melitta Kitzwoegerer Department of Pathology, University Hospital St. Poelten Karl Landsteiner University of Health Sciences, St. Poelten, Austria
  • Franz Payer Department of Neurology, Medical University of Graz, Graz, Austria
  • Julia J. Unterluggauer Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria
  • Johannes Haybaeck Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria; ;Department of Pathology, Otto-von-Guericke University of Magdeburg, Magdeburg, Germany
  • Günther Stockhammer Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria
  • Sarah Iglseder Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria
  • Patrizia Moser Department of Pathology, Medical University of Innsbruck, Innsbruck, Austria
  • Claudius Thomé Department of Neurosurgery, Medical University of Innsbruck, Innsbruck, Austria
  • Martin Stultschnig Department of Neurology, State Hospital Klagenfurt, Klagenfurt, Austria
  • Franz Wuertz Institute of Pathology, State Hospital Klagenfurt, Klagenfurt, Austria
  • Tanisa Brandner-Kokalj Institute of Pathology, State Hospital Klagenfurt, Klagenfurt, Austria
  • Serge Weis Department of Neuropathology, Neuromed Campus, Kepler University Hospital, Johannes Kepler University of Linz, Linz, Austria
  • Dave Bandke Department of Neuropathology, Neuromed Campus, Kepler University Hospital, Johannes Kepler University of Linz, Linz, Austria
  • Josef Pichler Department of Internal Medicine and Neurooncology, Neuromed Campus, Kepler University Hospital, Johannes Kepler University of Linz, Linz, Austria
  • Markus Hutterer Department of Neurology, Neuromed Campus, Kepler University Hospital, Johannes Kepler University of Linz, Linz, Austria
  • Karl J. Krenosz Department of Hematology and Oncology, Kepler University Hospital, Johannes Kepler University of Linz, Linz, Austria
  • Alexandra Boehm Department of Internal Medicine, Hematology and Oncology, Hospital Elisabethinen, Linz, Austria
  • Beate Mayrbaeurl Department of Internal Medicine IV, Hospital Wels-Grieskirchen, Wels-Grieskirchen, Austria
  • Andrea Hager-Seifert Department of Neurology, State Hospital Wiener Neustadt, Wiener Neustadt, Austria
  • Hannes Kaufmann Department of Oncology, Krankenanstalt Rudolfstiftung, Vienna, Austria
  • Martina Dumser Department of Pathology, Krankenanstalt Rudolfstiftung, Vienna, Austria
  • Angelika Reiner-Concin Department of Pathology, Donauspital Vienna, Vienna, Austria
  • Selma Hoenigschnabl Department of Pathology, Donauspital Vienna, Vienna, Austria
  • Waltraud Kleindienst Department of Neurology, Paracelsus Medical University Salzburg, Salzburg, Austria
  • Markus Hoffermann Department of Neurosurgery, State Hospital Feldkirch, Feldkirch, Austria
  • Karin Dieckmann Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria; ;Department of Radiotherapy, Medical University of Vienna, Vienna, Austria
  • Barbara Kiesel Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria; ;Department of Neurosurgery, Medical University of Vienna, Vienna, Austria
  • Georg Widhalm Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria; ;Department of Neurosurgery, Medical University of Vienna, Vienna, Austria
  • Christine Marosi Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria; ;Department of Medicine I, Medical University of Vienna, Vienna, Austria
  • Ulrich Jaeger Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria; ;Department of Medicine I, Medical University of Vienna, Vienna, Austria
  • Andreas Hainfellner Institute of Neurology, Medical University of Vienna, Vienna, Austria; ;Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria
  • Monika Hackl Austrian National Cancer Registry, Statistics Austria, Vienna, Austria
  • Johannes A. Hainfellner Institute of Neurology, Medical University of Vienna, Vienna, Austria; ;Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria
  • Matthias Preusser Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria; ;Department of Medicine I, Medical University of Vienna, Vienna, Austria
  • Adelheid Woehrer Institute of Neurology, Medical University of Vienna, Vienna, Austria; ;Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria

DOI:

https://doi.org/10.1080/0284186X.2019.1599137

Abstract

Background: Primary CNS lymphoma is a highly aggressive and rare type of extranodal non-Hodgkin lymphoma. Although, new therapeutic approaches have led to improved survival, the management of the disease poses a challenge, practice patterns vary across institutions and countries, and remain ill-defined for vulnerable patient subgroups.

Material and Methods: Using information from the Austrian Brain Tumor Registry we followed a population-based cohort of 189 patients newly diagnosed from 2005 to 2010 through various lines of treatment until death or last follow-up (12-31-2016). Prognostic factors and treatment-related data were integrated in a comprehensive survival analysis including conditional survival estimates.

Results: We find variable patterns of first-line treatment with increasing use of rituximab and high-dose methotrexate (HDMTX)-based poly-chemotherapy after 2007, paralleled by an increase in median overall survival restricted to patients aged below 70 years. In the entire cohort, 5-year overall survival was 24.4% while 5-year conditional survival increased with every year postdiagnosis.

Conclusion: In conclusion, we show that the use of poly-chemotherapy and immunotherapy has disseminated to community practice to a fair extent and survival has increased over time at least in younger patients. Annually increasing conditional survival rates provide clinicians with an adequate and encouraging prognostic measure.

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Published

2019-07-03

How to Cite

Neuhauser, M. ., Roetzer, T. ., Oberndorfer, S. ., Kitzwoegerer, M. ., Payer, F. ., Unterluggauer, J. J. ., … Woehrer, A. . (2019). Increasing use of immunotherapy and prolonged survival among younger patients with primary CNS lymphoma: a population-based study. Acta Oncologica, 58(7), 967–976. https://doi.org/10.1080/0284186X.2019.1599137