Surgery, Tamoxifen, Carboplatin, and Radiotherapy in the Treatment of Newly Diagnosed Glioblastoma Patients

被引:0
作者
Maximilian J.A. Puchner
Hans-Dietrich Herrmann
Jöurgen Berger
Loris Cristante
机构
[1] Gilead Hospital,Department of Neurosurgery; Department of Neurosurgery
[2] University Hospital Eppendorf,Department of Neurosurgery
[3] University Hospital Eppendorf,Institute of Mathematics and Computer Sciences in Medicine
[4] University of Manitoba,Department of Neurosurgery; Division of Neurosurgery
来源
Journal of Neuro-Oncology | 2000年 / 49卷
关键词
glioblastoma; glioma; tamoxifen; carboplatin; radiotherapy; protein kinase C;
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摘要
A historically controlled phase II study was undertaken to investigate the efficacy and toxicity of a postoperative treatment consisting of high-dose continuous tamoxifen, carboplatin and radiotherapy in patients with newly diagnosed glioblastoma. Between 1995 and 1998, 50 patients with newly diagnosed glioblastomas underwent surgery and were subsequently treated with 200 mg day−1 tamoxifen continuously, 3 cycles of carboplatin (300 mg m−2), and radiotherapy. Survival data for a historical control group were calculated from respective prognostic indices and were obtained from studies with comparable patient populations treated with operation and radiotherapy only. In our study, the median time to tumor progression was 30 weeks and the median survival time (MST) 55 weeks (95% confidence interval: 46–63 weeks). The MST of the control group (48 weeks) showed to be within this interval. In addition to already known prognostic factors in malignant gliomas (age, Karnofsky performance score, extent of tumor resection), the gender (females lived longer than males, p = 0.0025) showed to influence survival. Serious side effects (thrombosis, pulmonary embolism) occurred in 6 patients. A high incidence of multifocal tumor recurrences (33%), which might be related to study-treatment, was observed. In conclusion, the combined therapy failed to demonstrate a higher efficacy than standard treatment for glioblastoma patients.
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页码:147 / 155
页数:8
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共 147 条
[1]  
Legha SS(1988)Tamoxifen in the treatment of breast cancer Ann Intern Med 109 219-228
[2]  
Pollack IF(1990)Effect of tamoxifen on DNA synthesis and proliferation of human malignant glioma lines Cancer Res 50 7134-7138
[3]  
Randall MS(1990)Sex steroid receptors in intracranial tumors Cancer 65 1968-1970
[4]  
Kristofik MP(1993)Protein kinase C inhibitors suppress cell growth in established and low-passage glioma cell lines. A comparison between staurosporine and tamoxifen Neurosurgery 33 495-501
[5]  
Kelly RH(2000)Tamoxifen-resistant glioma-cell-subpopulations are characterized by increased migration and proliferation Int J Cancer 86 468-473
[6]  
Selker RG(1992)Protein kinase C activity correlates with the growth rate of malignant gliomas: part II: effects of glioma mitogens and modulators of protein kinase C Neurosurgery 31 717-724
[7]  
Vertosick FT(1992)Intracellular signaling by hydrolysis of phospholipids and activation of protein kinase C Science 258 607-614
[8]  
Stojkovic RR(1993)Clinical and radiographic response in a minority of patients with recurrent malignant gliomas treated with high-dose tamoxifen Neurosurgery 32 485-490
[9]  
Jovancevic M(1992)The treatment of intracranial malignant gliomas using orally administered tamoxifen therapy: preliminary results in a series of 'failed' patients Neurosurgery 30 897-903
[10]  
Santel DJ(1994)Tamoxifen: is it useful in the treatment of patients with metastatic melanoma? J Clin Oncol 12 617-626