Sustained focal antitumor activity of bevacizumab in recurrent glioblastoma.

نویسندگان

  • Oliver Bähr
  • Patrick N Harter
  • Lutz M Weise
  • Se-Jong You
  • Michel Mittelbronn
  • Michael W Ronellenfitsch
  • Johannes Rieger
  • Joachim P Steinbach
  • Elke Hattingen
چکیده

OBJECTIVES To investigate the relevance of bevacizumab (BEV)-induced diffusion-restricted lesions and T1-hyperintense lesions in patients with recurrent glioblastoma. METHODS We prospectively screened 74 BEV-treated patients with recurrent glioblastoma for (1) diffusion-restricted lesions and/or, (2) lesions with a hyperintense signal on precontrast T1-weighted images. We further evaluated overall survival (OS), histopathology of the lesions, and patterns of progression. RESULTS Twenty-five of 74 patients (34%) developed T1-hyperintense lesions, whereas diffusion-restricted lesions could be detected in 35 of 74 patients (47%). In 21 of 74 patients (28%), the lesions displayed both features ("double-positive"). OS for patients with double-positive lesions was 13.0 months; patients with neither of these lesions had an OS of 6.6 months (p < 0.005). Histologic evaluation of double-positive lesions revealed extensive calcified necrosis in 4 of 4 patients. Notably, these double-positive lesions were rarely involved in further tumor progression. However, they were associated with an increase in distant recurrences at BEV failure. CONCLUSIONS BEV-induced double-positive MRI lesions are a predictive imaging marker associated with a substantial survival benefit and with improved local control in patients with recurrent glioblastoma. Our data suggest that these lesions are the result of a sustained focal antitumor activity of BEV.

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عنوان ژورنال:
  • Neurology

دوره 83 3  شماره 

صفحات  -

تاریخ انتشار 2014