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A Phase II Trial With Cetuximab, Bevacizumab and Irinotecan for Patients With Malignant Glioblastomas and Progression After Radiation Therapy and Temozolamide
Irinotecan has demonstrated activity in malignant gliomas in multiple phase II studies. The activity is limited, with an approximately 15 % response rate and a progression-free survival of 3-5 months. Given the synergy between irinotecan and bevacizumab in colorectal cancer, and the high-level expression of vascular endothelial growth factor on malignant gliomas, one would expect synergy between bevacizumab and irinotecan against gliomas. In addition, 40-50 % of GBM have EGFR amplification/mutation making the EGFR an additional target. By combing cetuximab, with irinotecan and bevacizumab, one would expect further response, than irinotecan and bevacizumab alone. In addition, recurrent gliomas have an extremely poor prognosis, so innovative therapies are needed.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Aalborg University Hospital
Aalborg, Denmark
Rigshospitalet
Copenhagen, Denmark
Odense University Hospital
Odense, Denmark
Start Date
August 1, 2006
Primary Completion Date
December 1, 2008
Completion Date
December 1, 2008
Last Updated
December 11, 2008
32
ACTUAL participants
Cetuximab
DRUG
Bevacizumab
DRUG
Irinotecan
DRUG
Lead Sponsor
Rigshospitalet, Denmark
Collaborators
NCT01107522
NCT02388659
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