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卡铂和长春新碱化疗用于新诊断的进展性低级别胶质瘤儿童患者。

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

作者信息

Packer R J, Ater J, Allen J, Phillips P, Geyer R, Nicholson H S, Jakacki R, Kurczynski E, Needle M, Finlay J, Reaman G, Boyett J M

机构信息

Department of Neurology, Children's National Medical Center, George Washington University, Washington, D.C. 20010, USA.

出版信息

J Neurosurg. 1997 May;86(5):747-54. doi: 10.3171/jns.1997.86.5.0747.

Abstract

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.

摘要

儿童不可切除性低级别胶质瘤的最佳治疗方案仍未确定。对于年幼儿童使用化疗的关注度有所增加,但关于这种治疗的长期疗效的信息却很少。78名平均年龄为3岁(范围3个月至16岁)的新诊断为进展性低级别胶质瘤的儿童接受了卡铂和长春新碱联合化疗。从诊断开始,患者的中位随访时间为30个月,其中31名患者随访超过3年。58名儿童患有间脑肿瘤,12名患有脑干胶质瘤,3名患有弥漫性软脑膜胶质瘤。78名患者中有44名(56%)显示出客观的治疗反应。2年无进展生存率为75±6%,3年为68±7%。1型神经纤维瘤病患儿和无此病患儿的无进展生存率无统计学差异(2年无进展生存率分别为79±11%和75±6%)。肿瘤的组织学亚型、位置及其对化疗的最大反应对疾病控制的持续时间没有影响。唯一显著的预后因素是年龄:治疗时5岁及以下的儿童3年无进展生存率为74±7%,而年龄较大的儿童为39±21%(p<0.01)。卡铂和长春新碱治疗对于控制新诊断的进展性低级别胶质瘤有效,尤其是在年幼儿童中。

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