Phase II study of temozolomide and cisplatin as primary treatment prior to radiotherapy in newly diagnosed glioblastoma multiforme patients with measurable disease.: A study of the Spanish Medical Neuro-Oncology Group (GENOM)

被引:27
作者
Balaña, C
López-Pousa, A
Berrocal, A
Yaya-Tur, R
Herrero, A
García, JL
Martín-Broto, J
Benavides, M
Cerdá-Nicolás, M
Ballester, R
Balart, J
Capellades, J
机构
[1] Hosp Univ Germans Trias & Pujol, Inst Catala Oncol, Med Oncol Serv, Barcelona 08916, Spain
[2] Hosp Santa Creu & Sant Pau, Med Oncol Serv, Barcelona, Spain
[3] Hosp Gen Valencia, Med Oncol Serv, Valencia, Spain
[4] Inst Valenciano Oncol, Med Oncol Serv, Valencia, Spain
[5] Hosp Univ Miguel Servet, Med Oncol Serv, Zaragoza, Spain
[6] Hosp Ramon y Cajal, Med Oncol Serv, E-28034 Madrid, Spain
[7] Hosp Son Dureta, Med Oncol Serv, Palma de Mallorca, Spain
[8] Hosp Reg Carlos Haya, Med Oncol Serv, Malaga, Spain
[9] Hosp Clin Univ, Dept Patol, Pathol Cent Review, Valencia, Spain
[10] Hosp Univ Germans Trias & Pujol, Inst Catala Oncol, Oncol Serv, Barcelona, Spain
[11] Hosp Univ Germans Trias & Pujol, Inst Catala Oncol, Radiotherapy Serv, Barcelona, Spain
[12] Hosp Santa Creu & Sant Pau, Oncol Serv, Barcelona, Spain
[13] Hosp Santa Creu & Sant Pau, Radiotherapy Serv, Barcelona, Spain
[14] Hosp Univ Germans Trias & Pujol, Inst Diagnost Imatge, Radiol Cent Review, Barcelona, Spain
关键词
cisplatin; chemotherapy; glioblastoma; pre-radiotherapy; temozolomide;
D O I
10.1007/s11060-004-9175-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This phase II study evaluates the activity of temozolomide and cisplatin administered before radiation therapy in newly diagnosed glioblastoma multiforme patients, in terms of response, time to progression and survival. Patients and methods: Forty patients with measurable disease after surgery, a Karnofsky status> 60, and Barthel Index> 10 were included. They were treated with three cycles of temozolomide 200 mg/m(2)/day for 5 days and cisplatin 100 mg/m(2) on day 1. Conventional focal radiation therapy to 60 Gy was administered after response evaluation. Results: Three patients were not evaluable for central reviewed response but all 40 were evaluable for toxicity, time to progression and survival. Objective responses by Macdonald criteria on an intent to treat basis were 45% including complete response in three patients (7.5%), and partial response in 15 patients (37.5%). Responses were seen in biopsy-only patients (33.4%) as well as in partial surgery patients (52%). Median survival for all patients was 12.5 months. Biopsy-only patients had a median survival of 12.8 months. Grade 3 to 4 neutropenia was the most important toxicity, and occurred in 37.5% of patients. A delay in 18.2% and a dose reduction in 9.6% of cycles were necessary due to myelosuppression on day 28. Two patients had neutropenic fever resulting in one treatment-related death. Eighty-two percent of patients received radiotherapy. Conclusion: This regimen has significant activity, as it induces objective responses even in biopsy-only patients, appearing to improve their median survival. A better combination schedule is needed to improve the toxicity profile.
引用
收藏
页码:359 / 369
页数:11
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