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4岁以下恶性脑肿瘤患儿的术后化疗:基于VETOPEC方案的初步反应良好。澳大利亚和新西兰儿童癌症研究组(ANZCCSG)的一项研究

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).

作者信息

White L, Kellie S, Gray E, Toogood I, Waters K, Lockwood L, Macfarlane S, Johnston H

机构信息

Sydney Children's Hospital, NSW, Australia.

出版信息

J Pediatr Hematol Oncol. 1998 Mar-Apr;20(2):125-30. doi: 10.1097/00043426-199803000-00007.

Abstract

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.

摘要

目的

在一项多机构研究中,对4岁以下脑肿瘤患儿术后化疗并无限期推迟放疗进行了调查。

患者与方法

1991年至1995年,42例年龄在3至47个月(中位年龄20个月)的脑肿瘤患者纳入了一项两阶段化疗方案:16例为髓母细胞瘤(MB);8例为幕上原始神经外胚层肿瘤(PNET);14例为室管膜瘤;4例为其他肿瘤。初始阶段由4个疗程的三联药物方案组成:长春新碱(VCR)、依托泊苷(VP - 16)和强化环磷酰胺(CPA),采用先前报道的方案(VETOPEC)。延续阶段由两药疗程组成:A,CPA + VCR;B,顺铂 + VP - 16;C,卡铂 + VP - 16,总疗程为64周。

结果

28例术后有残留(25例)和/或转移(1例M2,6例M3)肿瘤的患者对VETOPEC的反应可评估。有9例完全缓解(CR)和9例部分缓解(PR),CR + PR合计为64%(95%置信区间[CI] 44%至81%)。在12例可评估的MB患者中,CR + PR为82%(48%至98%);在6例PNET患者中,为50%(12%至88%);在8例室管膜瘤患者中,为86%(42%至99%)。在40例符合进一步分析条件的患者中,6例在中位时间30个月时无进展,14例在中位时间38个月时存活,29例在中位时间7个月(范围2至37个月)时病情进展,26例死亡。36个月时的无进展生存率和总生存率估计分别为11%(95% CI 1%至22%)和34%(18%至50%)。

结论

VETOPEC方案的初始反应令人鼓舞,值得进一步研究剂量递增。在这个高危人群中,目前的治疗策略生存率仍然很低。

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