Postoperative chemotherapy in children less than 4 years of age with malignant brain tumors: Promising initial response to a VETOPEC-based regimen - A study of the Australian and New Zealand Children's Cancer Study Group (ANZCCSG)

被引:46
作者
White, L
Kellie, S
Gray, E
Toogood, I
Waters, K
Lockwood, L
Macfarlane, S
Johnston, H
机构
[1] New Childrens Hosp, Sydney, NSW, Australia
[2] Womens & Childrens Hosp, Adelaide, SA, Australia
[3] Royal Childrens Hosp, Melbourne, Vic, Australia
[4] Monash Hosp, Melbourne, Vic, Australia
[5] Royal Childrens Hosp, Brisbane, Qld 4029, Australia
[6] Univ Queensland, Mater Childrens Hosp, Brisbane, Qld 4101, Australia
[7] Univ Otago, Christchurch Hosp, Dunedin, New Zealand
[8] Starship Childrens Hlth, Auckland, New Zealand
[9] Sydney Childrens Hosp, Sydney, NSW, Australia
关键词
brain tumor; child; chemotherapy; cyclophosphamide;
D O I
10.1097/00043426-199803000-00007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Postoperative chemotherapy with indefinite postponement of radiation therapy in children <4 years old with brain tumors was investigated in a multi-institutional study. Patients and Methods: From 1991 to 1995, 42 patients aged 3 to 47 months (median 20) with brain tumors were enrolled in a 2-phase chemotherapy protocol: 16 patients had medulloblastoma (MB); 8 had supratentorial primitive neuroectodermal tumor (PNET); 14 had ependymoma; and 4 had other tumors. The initial phase was comprised of 4 courses of the 3-drug regimen: vincristine (VCR), etoposide (VP-16), and intensive cyclophosphamide (CPA) in a previously reported schedule (VETOPEC). The continuation phase was comprised of 2-drug courses: A, CPA + VCR; B, cisplatin + VP-16; and C, carboplatin + VP-16, for a total duration of 64 weeks. Results: Response to VETOPEC was evaluable in 28 patients with postresection residual (25) and/or metastatic (1 M2, 6 M3) tumor. There were 9 complete responses (CR) and 9 partial responses (PR) with a combined CR + PR of 64% (95% confidence interval [CI] 44 to 81). In 12 evaluable patients with MB, CR + PR was 82% (48 to 98); in 6 patients with PNET, 50% (12 to 88); and, in 8 patients with ependymoma, 86% (42 to 99). Of 40 patients eligible for further analysis, 6 remain progression-free at a median of 30 months, 14 are alive at a median of 38 months, 29 have progressed at a median of 7 months (range, 2 to 37 months), and 26 have died. The progression-free and overall survival rates at 36 months are estimated to be 11% (95% CI 1 to 22) and 34% (18 to 50), respectively. Conclusions: The initial response to the VETOPEC regimen is encouraging and warrants study of further dose escalation. Survival remains poor with current strategies in this high-risk population.
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页码:125 / 130
页数:6
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