RNOP-09: Pegylated liposomal doxorubicine and prolonged temozolomide in addition to radiotherapy in newly diagnosed glioblastoma - a phase II study

被引:104
作者
Beier, Christoph P. [1 ]
Schmid, Christina [1 ]
Gorlia, Thierry [2 ]
Kleinletzenberger, Christine [1 ]
Beier, Dagmar [1 ]
Grauer, Oliver [1 ]
Steinbrecher, Andreas [1 ]
Hirschmann, Birgit [1 ]
Brawanski, Alexander [3 ]
Dietmaier, Christopher [4 ]
Jauch-Worley, Tanja [1 ]
Koelbl, Oliver [5 ]
Pietsch, Torsten [6 ]
Proescholdt, Martin [3 ]
Ruemmele, Petra [7 ]
Muigg, Armin [8 ]
Stockhammer, Guenther [8 ]
Hegi, Monika [9 ,10 ]
Bogdahn, Ulrich [1 ]
Hau, Peter [1 ]
机构
[1] Univ Regensburg, Dept Neurol, D-93053 Regensburg, Germany
[2] Eortc Data Ctr, B-1200 Brussels, Belgium
[3] Univ Regensburg, Dept Neurosurg, D-93053 Regensburg, Germany
[4] Univ Appl Sci Amberg Weiden, D-92224 Weiden, Germany
[5] Univ Regensburg, Dept Radiooncol, D-93053 Regensburg, Germany
[6] Univ Bonn, Dept Neuropathol, D-53015 Bonn, Germany
[7] Dept Pathol, D-93053 Regensburg, Germany
[8] Univ Innsbruck, Dept Neurol, A-6020 Innsbruck, Austria
[9] Ctr Univ Romands Neurochirurg, Lab Brain Tumor Biol & Genet, CH-1011 Lausanne, Switzerland
[10] Univ Lausanne, CH-1011 Lausanne, Switzerland
关键词
METASTATIC BREAST-CARCINOMA; HIGH-GRADE GLIOMA; MALIGNANT GLIOMA; O-6-METHYLGUANINE-DNA METHYLTRANSFERASE; RESPONSE CRITERIA; RECURRENT GLIOMA; EFFICACY; CHEMOTHERAPY; TOXICITY; MODEL;
D O I
10.1186/1471-2407-9-308
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Although Temozolomide is effective against glioblastoma, the prognosis remains dismal and new regimens with synergistic activity are sought for. Methods: In this phase-I/II trial, pegylated liposomal doxorubicin (Caelyx (TM), PEG-Dox) and prolonged administration of Temozolomide in addition to radiotherapy was investigated in 63 patients with newly diagnosed glioblastoma. In phase-I, PEG-Dox was administered in a 3-by-3 dose-escalation regimen. In phase-II, 20 mg/m(2) PEG-Dox was given once prior to radiotherapy and on days 1 and 15 of each 28-day cycle starting 4 weeks after radiotherapy. Temozolomide was given in a dose of 75 mg/m(2) daily during radiotherapy (60 Gy) and 150-200 mg/m(2) on days 1-5 of each 28-day cycle for 12 cycles or until disease progression. Results: The toxicity of the combination of PEG-Dox, prolonged administration of Temozolomide, and radiotherapy was tolerable. The progression free survival after 12 months (PFS-12) was 30.2%, the median overall survival was 17.6 months in all patients including the ones from Phase-I. None of the endpoints differed significantly from the EORTC26981/NCIC-CE.3 data in a post-hoc statistical comparison. Conclusion: Together, the investigated combination is tolerable and feasible. Neither the addition of PEG-Dox nor the prolonged administration of Temozolomide resulted in a meaningful improvement of the patient's outcome as compared to the EORTC26981/NCIC-CE.3 data
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页数:10
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