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A Phase II trial of tandutinib (MLN 518) in combination with bevacizumab for patients with recurrent glioblastoma.


ABSTRACT: A Phase II trial of bevacizumab plus tandutinib.We enrolled 41 recurrent, bevacizumab-naive glioblastoma patients for a trial of bevacizumab plus tandutinib. Median age was 55 and 71% were male. Treatment consisted of tandutinib 500 mg two-times a day (b.i.d.) and bevacizumab 10 mg/kg every 2 weeks starting day 15. Of 37 (90%) evaluable, nine (24%) had partial response.Median overall and progression-free survival was 11 and 4.1 months; progression-free survival at 6 months was 23%. All patients suffered treatment-related toxicities; common grade ?3 toxicities were hypertension (17.1%), muscle weakness (17.1%), lymphopenia (14.6%) and hypophosphatemia (9.8%). Four of six with grade ?3 tandutinib-related myasthenic-like muscle weakness had electromyography-proven neuromuscular junction pathology. Tandutinib with bevacizumab was as effective but more toxic than bevacizumab monotherapy.

SUBMITTER: Odia Y 

PROVIDER: S-EPMC5514626 | biostudies-literature | 2016

REPOSITORIES: biostudies-literature

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A Phase II trial of tandutinib (MLN 518) in combination with bevacizumab for patients with recurrent glioblastoma.

Odia Yazmin Y   Sul Joohee J   Shih Joanna H JH   Kreisl Teri N TN   Butman John A JA   Iwamoto Fabio M FM   Fine Howard A HA  

CNS oncology 20160210 2


<h4>Aim</h4>A Phase II trial of bevacizumab plus tandutinib.<h4>Methods</h4>We enrolled 41 recurrent, bevacizumab-naive glioblastoma patients for a trial of bevacizumab plus tandutinib. Median age was 55 and 71% were male. Treatment consisted of tandutinib 500 mg two-times a day (b.i.d.) and bevacizumab 10 mg/kg every 2 weeks starting day 15. Of 37 (90%) evaluable, nine (24%) had partial response.<h4>Results & conclusion</h4>Median overall and progression-free survival was 11 and 4.1 months; pro  ...[more]

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