A multicenter retrospective study of chemotherapy for recurrent intracranial ependymal tumors in adults by the Gruppo Italiano Cooperativo di Neuro-Oncologia

被引:60
作者
Brandes, AA
Cavallo, G
Reni, M
Tosoni, A
Nicolardi, L
Scopece, L
Franceschi, E
Sotti, G
Talacchi, A
Turazzi, S
Ermani, M
机构
[1] Azienda Osped Univ, Dept Med Oncol, I-35100 Padua, Italy
[2] Osped Bellaria, Dept Med Oncol, Bologna, Italy
[3] Univ Milan, Osped San Raffaele, I-20127 Milan, Italy
[4] Univ Padua, Azienda Osped, Dept Radiotherapy, Padua, Italy
[5] Univ Hosp Verona, Dept Neurosurg, Verona, Italy
[6] Univ Padua, AZienda Osped, Dept Neurol Sci, Padua, Italy
关键词
ependymomas; adults; recurrent; chemotherapy; prognostic factors; clinical trials;
D O I
10.1002/cncr.21110
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. No data on the role of chemotherapy in recurrent ependymal tumors are available in adults. The aim of the current study was to investigate outcomes after salvage chemotherapy in this setting, METHODS. A retrospective review was made of the charts of 28 adults (>= 18 years) with progressive or recurrent ependymal tumors after surgery and radiotherapy, who received chemotherapy between 1993 and 2003 in 3 institutions of the Gruppo Italiano Cooperativo di Neuro-Oncologia network. RESULTS. Thirteen patients (46.3%) received cisplatin-based chemotherapy (Group A) and 15 (53.7%) received regimens without cisplatin (Group 13). Platinum-based chemotherapy yielded 2 complete responses (CR) (15.4%) and 2 (15.4%) partial responses (PR), whereas 7 patients (53.8%) remained stable (SD). After regimens without cisplatin, there were no CR, 2 PR (13.3%), and 11 SD (73.3%). The overall median time to progression was 9.9 months (95% confidence interval [95% CI], 7.5-21.7 months), 9.9 months (5.2-not reached) for Group A and 10.9 months (95% CI, 7.17-23.9 months) for Group B. The overall median survival (OS) was 40.7 months (95% Cl, 16-not reached), 31 months (21-not reached) for Group A and 40.7 months (13.4-not reached) for Group B. CONCLUSIONS. Cisplatin-based chemotherapy achieved a higher response rate, but did not prolong disease progression-free survival or OS. More active regimens for the salvage treatment of ependymal tumors have yet to be found. (c) 2005 American Cancer Society.
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收藏
页码:143 / 148
页数:6
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