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      Increased survival of glioblastoma patients who respond to antiangiogenic therapy with elevated blood perfusion.

      Cancer research
      Angiogenesis Inhibitors, therapeutic use, Brain Neoplasms, blood supply, drug therapy, pathology, Disease Progression, Disease-Free Survival, Glioblastoma, Humans, Magnetic Resonance Imaging, Neoplasm Recurrence, Local, Quinazolines, Receptors, Vascular Endothelial Growth Factor, antagonists & inhibitors, Survival Rate
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          Abstract

          The abnormal vasculature of the tumor microenvironment supports progression and resistance to treatment. Judicious application of antiangiogenic therapy may normalize the structure and function of the tumor vasculature, promoting improved blood perfusion. However, direct clinical evidence is lacking for improvements in blood perfusion after antiangiogenic therapy. In this study, we used MRI to assess tumor blood perfusion in 30 recurrent glioblastoma patients who were undergoing treatment with cediranib, a pan-VEGF receptor tyrosine kinase inhibitor. Tumor blood perfusion increased durably for more than 1 month in 7 of 30 patients, in whom it was associated with longer survival. Together, our findings offer direct clinical evidence in support of the hypothesis that vascular normalization can increase tumor perfusion and help improve patient survival.

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