Survival improvement in patients with glioblastoma multiforme during the last 20 years in a single tertiary-care center

被引:20
作者
Fazeny-Dörner, B
Gyries, A
Rössler, K
Ungersböck, K
Czech, T
Budinsky, A
Killer, M
Dieckmann, K
Piribauer, M
Baumgartner, G
Prayer, D
Veitl, M
Muhm, M
Marosi, C
机构
[1] Univ Vienna, Div Clin Oncol, A-1010 Vienna, Austria
[2] Univ Vienna, Ludwig Boltzmann Inst Clin Expt Oncol, Dept Med 1, A-1010 Vienna, Austria
[3] Univ Vienna, Dept Neurosurg, A-1010 Vienna, Austria
[4] Univ Vienna, Dept Radiooncol, A-1010 Vienna, Austria
[5] Lainz Hosp, Med Dept 5, Vienna, Austria
[6] Dept Anesthesiol, Vienna, Austria
[7] Dept Neuroradiol, Vienna, Austria
[8] Clin Inst Med & Chem Lab Diagnost, Vienna, Austria
关键词
Glioblastoma multiforme; adult; neuro-surgery; stereotactic biopsy; radiotherapy; concomitant chemotherapy; nitrosourea; fotemustine; dacarbazine;
D O I
10.1007/BF03040358
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Methodology: The survival of 357 consecutive patients with newly diagnosed glioblastoma multiforme (GBM) in three treatment groups reflecting different time-periods of diagnosis (A: 1982-1984; B: 1994/1995; C: 1996-1998) was analysed to assess the impact and the potential improvement of changing treatment strategies in our tertiary-care center. Patients and methods: Group A (n = 100) included all consecutive patients diagnosed from 1982 to 1984 and served as the historical control. Group B (n = 93) included all consecutive patients diagnosed in 1994/1995 and group C (n = 164) those diagnosed from 1996 to 1998. Survival in the three treatment groups (A vs. B vs. C) was analysed according to treatment given after neurosurgical intervention (i.e. no specific therapy versus radiotherapy versus combined radio-/chemotherapy), and according to first-line chemotherapy, age (<40, 40-60, >60), sex, and tumor location (hemispheric versus bilateral or multifocal tumors, and tumors involving eloquent brain areas). Survival was analysed using Kaplan-Meier's non-parametric method. A p-value <0.05 was considered statistically significant. Results: Patients in groups A and B received radio-and/or chemotherapy to a varying extent (radiotherapy: group A: 22%, group B: 62%; chemotherapy: group A: 6%, group B: 33%). Chemotherapy was administered after termination of radiotherapy in both groups. In group C, 96% of patients received combined radio-/chemotherapy which was administered concomitantly and started within three weeks after surgery. Median survival was 5.2 months in group A, 5.1 months in group B and 14.5 months in C (p<0.0001). Nine patients in group A (9%), 9 in group B (10%) and 40 in group C (25%) survived more than 18 months (p<0.05). Conclusions: Survival improvement in group C might be attributable to the early start of combined radio-/chemotherapy. Therapy was administered on a complete outpatient basis, enabled by a dedicated interdisciplinary neuro-oncologic team caring for group C. Toxicity was mild and patients' acceptance excellent.
引用
收藏
页码:389 / 397
页数:9
相关论文
共 51 条
[1]
Afra D, 2002, LANCET, V359, P1011
[2]
Boron neutron capture therapy of brain tumors - Current status and future prospects - Preface [J].
Barth, RF ;
Soloway, AH .
JOURNAL OF NEURO-ONCOLOGY, 1997, 33 (1-2) :3-7
[3]
A MEDICAL-RESEARCH-COUNCIL TRIAL OF 2 RADIOTHERAPY DOSES IN THE TREATMENT OF GRADE-3 AND GRADE-4 ASTROCYTOMA [J].
BLEEHEN, NM ;
STENNING, SP .
BRITISH JOURNAL OF CANCER, 1991, 64 (04) :769-774
[4]
Multicentre CRC phase II trial of temozolomide in recurrent or progressive high-grade glioma [J].
Bower, M ;
Newlands, ES ;
Bleehen, NM ;
Brada, M ;
Begent, RJH ;
Calvert, H ;
Colquhoun, I ;
Lewis, P ;
Brampton, MH .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1997, 40 (06) :484-488
[5]
Brada M, 2000, SEMIN ONCOL, V27, pS11
[6]
Brandes AA, 1996, J NEURO-ONCOL, V30, P247
[7]
PLACEBO-CONTROLLED TRIAL OF SAFETY AND EFFICACY OF INTRAOPERATIVE CONTROLLED DELIVERY BY BIODEGRADABLE POLYMERS OF CHEMOTHERAPY FOR RECURRENT GLIOMAS [J].
BREM, H ;
PIANTADOSI, S ;
BURGER, PC ;
WALKER, M ;
SELKER, R ;
VICK, NA ;
BLACK, K ;
SISTI, M ;
BREM, S ;
MOHR, G ;
MULLER, P ;
MORAWETZ, R ;
SCHOLD, SC .
LANCET, 1995, 345 (8956) :1008-1012
[8]
Burton Eric, 1999, Current Opinion in Oncology, V11, P157, DOI 10.1097/00001622-199905000-00003
[9]
Intra-arterial carboplatin chemotherapy for brain tumors: A dose escalation study based on cerebral blood flow [J].
Cloughesy, TF ;
Gobin, YP ;
Black, KL ;
Vinuela, F ;
Taft, F ;
Kadkhoda, B ;
Kabbinavar, F .
JOURNAL OF NEURO-ONCOLOGY, 1997, 35 (02) :121-131
[10]
Malignant glioma: Who benefits from adjuvant chemotherapy? [J].
DeAngelis, LM ;
Burger, PC ;
Green, SB ;
Cairncross, JG .
ANNALS OF NEUROLOGY, 1998, 44 (04) :691-695