Phase II trial of temozolomide and pegylated liposomal doxorubicin in the treatment of patients with glioblastoma multiforme following concurrent radiotherapy and chemotherapy
Field | Value | Language |
dc.contributor.author | Ananda, Sumitra | |
dc.contributor.author | Nowak, Anna | |
dc.contributor.author | Cher, Lawrence | |
dc.contributor.author | Dowling, Anthony | |
dc.contributor.author | Brown, Chris | |
dc.contributor.author | Simes, John | |
dc.contributor.author | Rosenthal, Mark A | |
dc.date.accessioned | 2015-12-10 | |
dc.date.available | 2015-12-10 | |
dc.date.issued | 2011-08-02 | |
dc.identifier.citation | Ananda S, Nowak A, Cher L, Dowling A, Brown C, Simes J, Rosenthal M, and for the Cooperative Trials Group for Neuro-Oncology (COGNO). Phase 2 trial of temozolomide and pegylated liposomal doxorubicin in the treatment of patients with glioblastoma multiforme following concurrent radiotherapy and chemotherapy. Journal of Clinical Neuroscience 2011; 18(11): 1444–1448. | en_AU |
dc.identifier.uri | http://hdl.handle.net/2123/14128 | |
dc.description.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, 200 mg/m2 orally) and PLD (day 1, 40 mg/m2 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. | en_AU |
dc.description.sponsorship | Schering-Plough and by Cancer Australia | en_AU |
dc.language.iso | en | en_AU |
dc.publisher | Elsevier | en_AU |
dc.subject | glioblastoma | en_AU |
dc.subject | temozolomide | en_AU |
dc.subject | Pegylated liposomal doxorubicin | en_AU |
dc.subject | phase 2 trial | en_AU |
dc.title | Phase II trial of temozolomide and pegylated liposomal doxorubicin in the treatment of patients with glioblastoma multiforme following concurrent radiotherapy and chemotherapy | en_AU |
dc.type | Article | en_AU |
dc.type.pubtype | Pre-print | en_AU |
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