4.8 Article

Increased Survival of Glioblastoma Patients Who Respond to Antiangiogenic Therapy with Elevated Blood Perfusion

Journal

CANCER RESEARCH
Volume 72, Issue 2, Pages 402-407

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-11-2464

Keywords

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Categories

Funding

  1. NCI/NIH [R21CA117079, R01CA129371, K24CA125440]
  2. NIH [S10RR023401, S10RR019307, S10RR019254, S10RR023043, S10RR021110, R01CA137254, 5R01NS060918, UL1 RR025758]
  3. NCI [P01CA80124]
  4. Saic-Frederick Inc. [26XS263]
  5. Norwegian Research Council [191088/V50]
  6. Harvard Catalyst grant [M01-RR-01066]
  7. Merck
  8. Sanofi-Aventis
  9. Genentech
  10. Novartis
  11. Medimmune
  12. AstraZeneca
  13. Amgen
  14. Vascular Biogenics
  15. Genzyme
  16. Millennium
  17. Pfizer
  18. Dyax
  19. Roche

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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. Cancer Res; 72(2); 402-7. (C)2011 AACR.

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