Carboplatin and vincristine chemotherapy for children with newly diagnosed progressive low-grade gliomas

被引:415
作者
Packer, RJ
Ater, J
Allen, J
Phillips, P
Geyer, R
Nicholson, HS
Jakacki, R
Kurczynski, E
Needle, M
Finlay, J
Reaman, G
Boyett, JM
机构
[1] GEORGE WASHINGTON UNIV, CHILDRENS NATL MED CTR, DEPT PEDIAT, WASHINGTON, DC USA
[2] GEORGE WASHINGTON UNIV, CHILDRENS NATL MED CTR, DEPT HEMATOL ONCOL, WASHINGTON, DC USA
[3] MD ANDERSON CANC CTR, DIV PEDIAT, HOUSTON, TX 77030 USA
[4] NYU MED CTR, DEPT NEUROONCOL, NEW YORK, NY 10016 USA
[5] UNIV PENN, CHILDRENS HOSP, DEPT NEUROL, PHILADELPHIA, PA 19104 USA
[6] UNIV PENN, CHILDRENS HOSP, DEPT ONCOL, PHILADELPHIA, PA 19104 USA
[7] UNIV WASHINGTON, CHILDRENS HOSP & MED CTR, DEPT ONCOL, SEATTLE, WA USA
[8] TEXAS SCOTTISH RITE HOSP CHILDREN, DEPT ONCOL, INDIANAPOLIS, IN USA
[9] MEM SLOAN KETTERING CANC CTR, DEPT PEDIAT ONCOL, NEW YORK, NY USA
[10] ST JUDE CHILDRENS RES HOSP, DEPT BIOSTAT, MEMPHIS, TN 38105 USA
关键词
glioma; chiasmatic glioma; low-grade glioma; brainstem tumor; chemotherapy; children;
D O I
10.3171/jns.1997.86.5.0747
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The optimum treatment of nonresectable low-grade gliomas of childhood remains undecided. There has been increased interest in the use of chemotherapy for young children, but little information concerning the long-term efficacy of such treatment. Seventy-eight children with a mean age of 3 years (range 3 months-16 years) who had newly diagnosed, progressive low-grade gliomas were treated with combined carboplatin and vincristine chemotherapy. The patients were followed for a median of 30 months from diagnosis, with 31 patients followed for more than 3 years. Fifty-eight children had diencephalic tumors, 12 had brainstem gliomas, and three had diffuse leptomeningeal gliomas. Forty-four (56%) of 78 patients showed an objective response to treatment. Progression-free survival rates were 75 +/- 6% at 2 years and 68 +/- 7% at 3 years. There was no statistical difference in progression-free survival rates between children with neurofibromatosis Type 1 and those without the disease (2-year, progression-free survival 79 +/- 11% vs. 75 +/- 6%, respectively). The histological subtype of the tumor, its location, and its maximum response to chemotherapy did not have an impact on the duration of disease control. The only significant prognostic factor was age: children 5 years old or younger at the time of treatment had a 3-year progression-free survival rate of 74 +/- 7% compared with a rate of 39 +/- 21% in older children (p < 0.01). Treatment with carboplatin and vincristine is effective, especially in younger children, in controlling newly diagnosed progressive low-grade gliomas.
引用
收藏
页码:747 / 754
页数:8
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