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顺铂/长春新碱化疗用于幼儿下丘脑/视路星形细胞瘤

Cisplatin/vincristine chemotherapy for hypothalamic/visual pathway astrocytomas in young children.

作者信息

Kato T, Sawamura Y, Tada M, Ikeda J, Ishii N, Abe H

机构信息

Department of Neurosurgery, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

J Neurooncol. 1998 May;37(3):263-70. doi: 10.1023/a:1005866021835.

DOI:10.1023/a:1005866021835
PMID:9524084
Abstract

Hypothalamic/visual pathway astrocytomas in children are usually quiescent, but certain cases contain aggressive neoplasms that cause progressive neurological and visual deterioration. Radiotherapy is not recommended in young children because of its adverse effects later in life. This report describes the efficacy of a chemotherapeutic regimen. Four young children with hypothalamic/visual pathway astrocytoma, with a mean of 18 months of age at diagnosis, were treated with chemotherapy. Three patients had diencephalic syndrome at the disease's onset. Three patients with pilocytic astrocytoma were histologically verified, and another infant was clinically diagnosed. A combination chemotherapy using cisplatin and vincristine was administered in a total of 8 cycles in 3 children and 4 in one child. One patient who demonstrated renal insufficiency after 4 cycles of this regimen was treated with additional 4 cycles using carboplatin instead of cisplatin. The acute and subacute hematologic and otologic toxicities were mild, and a transient renal insufficiency in a child during chemotherapy improved. After chemotherapy, tumor regression was documented in 3 patients, and the disease was observed to be stable in one patient with an evidence of intratumoral necrosis on MRI. Three patients showed neurological and endocrinological improvements. These results suggest that this regimen is feasible in young children and may be useful as a first-line treatment for hypothalamic/visual pathway astrocytomas, which in turn may allow potentially deleterious irradiation on the maturing brain to be deferred until the disease progresses.

摘要

儿童下丘脑/视路星形细胞瘤通常生长缓慢,但某些病例存在侵袭性肿瘤,可导致进行性神经功能和视力恶化。由于放疗对儿童后期生活有不良影响,因此不建议对幼儿进行放疗。本报告描述了一种化疗方案的疗效。4名诊断时平均年龄为18个月的下丘脑/视路星形细胞瘤幼儿接受了化疗。3例患者在疾病发作时出现间脑综合征。3例毛细胞型星形细胞瘤患者经组织学证实,另1例婴儿经临床诊断。3名儿童共接受了8个周期的顺铂和长春新碱联合化疗,1名儿童接受了4个周期。1例患者在该方案4个周期后出现肾功能不全,随后使用卡铂替代顺铂又接受了4个周期的治疗。急性和亚急性血液学及耳毒性较轻,1名儿童化疗期间出现的短暂肾功能不全有所改善。化疗后,3例患者肿瘤缩小,1例患者疾病稳定,MRI显示肿瘤内有坏死。3例患者神经功能和内分泌功能有所改善。这些结果表明,该方案对幼儿可行,可能作为下丘脑/视路星形细胞瘤的一线治疗方法,从而可能将对发育中大脑有潜在危害的放疗推迟到疾病进展时进行。

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