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Phase 2 trial of temozolomide and pegylated liposomal doxorubicin in the treatment of patients with glioblastoma multiforme following concurrent radiotherapy and chemotherapy
Abstract
Concurrent and post-radiotherapy temozolomide (T) significantly improves survival in patient with newly diagnosed glioblastoma multiforme. We aimed to assess the activity of the combination of T and pegylated liposomal doxorubicin (PLD) in this population. A combination of T (days 1-5, 200mg/m(2) orally) and PLD (day 1, 40 mg/m(2) intravenous) was given every 4 weeks for six cycles following chemo-radiotherapy as a post-operative treatment. The primary endpoint was 6-month progression free survival (6PFS). Of the 40 patients who enrolled (53 years median age, 73% male), the 6PFS was 58% (95% confidence interval [CI], 41-72%). The median time to progression was 6.2 months (95% CI, 5.6-8.0 months) and overall survival (OS) was 13.4 months (95% CI, 12.7-15.8 months). Thirty-four patients had measurable disease: one had a complete response (3%), 28 had stable disease (82%), and five had progressive disease (15%). Treatment was well tolerated: hematological toxicity included grade 3 neutropenia (8%). Grade 3 non-hematologic toxicity included nausea and vomiting (8%) and palmar-plantar toxicity (5%). We concluded that combination T and PLD is well tolerated but does not add significant clinical benefit regarding 6PFS and OS.
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The effects of pegylated liposomal doxorubicin (Doxil or Caelyx) in glioblastoma are unconvincing.
“The effects of a pegylated liposomal doxorubicin (Doxil or Caelyx) have recently been investigated in glioblastoma, but the results obtained are unconvincing (Glas et al., 2007;Beier et al., 2009;Ananda et al., 2011).”
From The association of statins plus LDL receptor‐targeted liposome‐encapsulated doxorubicin increases in vitro drug delivery across blood–brain barrier cells (2012) · cites this paper as Ananda et al., 2011
Phase I/II trials with pegylated liposomal doxorubicin have shown that the drug has very few side effects and is well tolerated, but does not offer a significant advantage in overall survival or progression-free survival compared to standard protocols.
“Phase I/II trials with pegylated liposomal doxorubicin have shown that the drug has very few side effects and is well tolerated, but does not offer a significant advantage in terms of overall survival or progression-free survival in comparison to the standard protocols based on radio-chemotherapy (Glas et al., 2007;Beier et al., 2009;Ananda et al., 2011).”
From The association of statins plus LDL receptor‐targeted liposome‐encapsulated doxorubicin increases in vitro drug delivery across blood–brain barrier cells (2012) · cites this paper as Ananda et al., 2011
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Multicenter phase II trial of temozolomide in patients with glioblastoma multiforme at first relapse
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Vieira, D., & Gamarra, L. (2016) · International Journal of Nanomedicine · doi:10.2147/ijn.s117210 · Cited by 427
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Metadata
- Authors
- Ananda, S., Nowak, A. K., Cher, L., Dowling, A., Brown, C., Simes, J., & Rosenthal, M. A.
- Venue
- Journal of Clinical Neuroscience
- Publisher
- Elsevier BV
- Published
- 2011-11
- Volume
- 18
- Issue
- 11
- Pages
- 1444-1448
- ISSN
- 0967-5868
- Cited by
- 116
- References
- 2
- Language
- en
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