Radiation and concomitant weekly administration of paclitaxel in patients with glioblastoma multiforme. A phase II study

被引:21
作者
Fountzilas, G
Karavelis, A
Capizzello, A
Kalogera-Fountzila, A
Karkavelas, G
Zamboglou, N
Selviaridis, P
Foroglou, G
Tourkantonis, A
机构
[1] Aristotle Univ Thessaloniki, AHEPA Hosp, Dept Neurosurg, Thessaloniki 54636, Macedonia, Greece
[2] Aristotle Univ Thessaloniki, AHEPA Hosp, Dept Radiat, Thessaloniki 54636, Macedonia, Greece
[3] Aristotle Univ Thessaloniki, AHEPA Hosp, Dept Radiol, Thessaloniki 54636, Macedonia, Greece
[4] Aristotle Univ Thessaloniki, AHEPA Hosp, Dept Pathol, Thessaloniki 54636, Macedonia, Greece
[5] Stadt Kliniken, Dept Radiat Oncol, Offenbach, Germany
[6] Aristotle Univ Thessaloniki, AHEPA Hosp, Dept Internal Med, Thessaloniki 54636, Macedonia, Greece
关键词
radiotherapy; chemotherapy; paclitaxel; brain tumors;
D O I
10.1023/A:1006386114104
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The present study was conducted to evaluate the activity and toxicity profile of radiation (RT) and concomitant chemotherapy in patients with glioblastoma multiforme (GBM). Thirty-nine patients were treated postoperatively with RT and concomitant administration of paclitaxel. Cranial irradiation was initiated 2-3 weeks postoperatively and was administered in 2.0 fractions, one fraction per day, for 5 consecutive days per week, to a total of 60 Gy. Paclitaxel was delivered at a dose of 100 mg/m(2) over 3-h once weekly for 6 weeks. Thirty-three patients received all 6 cycles of paclitaxel according to the protocol. Totally, 217 cycles were delivered all of them at full dose. The median relative dose intensity of paclitaxel was (range 0.88-1.1). Three (7.5%) patients achieved complete and 9 (23%) partial response, while 12 (30.5%) patients demonstrated stabilization of the disease. Side effects from combined chemoradiotherapy were mainly mild. Grade III toxicity included infection (7.5%) and alopecia (5%). Median time to progression was 6 (range 0.9-27) months and median survival 10.7 (range 0.9-39.5+) months. The present study has clearly shown that 100 mg/m(2) of paclitaxel in 1-h infusion weekly can be safely given concomitantly with RT in patients with GBM with manageable toxicity. However, the efficacy of this combined modality treatment does not appear to be superior to that of RT alone.
引用
收藏
页码:159 / 165
页数:7
相关论文
共 35 条
[1]   p53 protein in pediatric malignant astrocytomas: A study of 21 patients [J].
Bhattacharjee, MB ;
Bruner, JM .
JOURNAL OF NEURO-ONCOLOGY, 1997, 32 (03) :225-233
[2]   CANCER STATISTICS, 1994 [J].
BORING, CC ;
SQUIRES, TS ;
TONG, T ;
MONTGOMERY, S .
CA-A CANCER JOURNAL FOR CLINICIANS, 1994, 44 (01) :7-26
[3]   Incidence and risk of thromboembolism during treatment of high-grade gliomas: a prospective study [J].
Brandes, AA ;
Scelzi, E ;
Salmistraro, G ;
Ermani, M ;
Carollo, C ;
Berti, F ;
Zampieri, P ;
Baiocchi, C ;
Fiorentino, MV .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (10) :1592-1596
[4]  
BRIASOULIS E, 1997, P AN M AM SOC CLIN, V16, P812
[5]  
BURGER PC, 1985, CANCER, V56, P1106, DOI 10.1002/1097-0142(19850901)56:5<1106::AID-CNCR2820560525>3.0.CO
[6]  
2-2
[7]  
CAHAN MA, 1994, CANCER CHEMOTH PHARM, V33, P441, DOI 10.1007/BF00686276
[8]   SALVAGE CHEMOTHERAPY WITH PACLITAXEL FOR RECURRENT PRIMARY BRAIN-TUMORS [J].
CHAMBERLAIN, MC ;
KORMANIK, P .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (08) :2066-2071
[9]   Phase I study of paclitaxel in patients with recurrent malignant glioma: A North American brain tumor consortium report [J].
Chang, SM ;
Kuhn, JG ;
Rizzo, J ;
Robins, HI ;
Schold, SC ;
Spence, AM ;
Berger, MS ;
Mehta, MP ;
Bozik, ME ;
Pollack, I ;
Gilbert, M ;
Fulton, D ;
Rankin, C ;
Malec, M ;
Prados, MD .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (06) :2188-2194
[10]  
CHERUKU R, 1991, CANCER, V68, P2621, DOI 10.1002/1097-0142(19911215)68:12<2621::AID-CNCR2820681218>3.0.CO