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剂量密集诱导化疗的一项初步研究中“高危”儿童脑肿瘤的差异反应性

Differential responsiveness among "high risk" pediatric brain tumors in a pilot study of dose-intensive induction chemotherapy.

作者信息

Jennings Mark T, Cmelak Anthony, Johnson Mahlon D, Moots Paul L, Pais Ray, Shyr Yu

机构信息

Department of Neurology, Vanderbilt-Ingram Cancer Center, Nashville, Tennessee, USA.

出版信息

Pediatr Blood Cancer. 2004 Jul;43(1):46-54. doi: 10.1002/pbc.20043.

Abstract

BACKGROUND

These factors have been predictive for progressive disease on therapy (PDOT) among pediatric brain tumors: >1.5 cm(2) unresectable tumor, glioblastoma, supratentorial primitive neuroectodermal tumor, and metastatic medulloblastoma (MBL). This pilot study sought to correlate cytoreductive response with progression free survival.

PROCEDURES

Four courses of cisplatinum, cyclophosphamide, etoposide, and vincristine preceded hyperfractionated radiotherapy (RT). Maintenance chemotherapy consisted of eight cycles of carboplatin, etoposide, and vincristine. Biopsy specimens were immunohistochemically studied for labeling index, hypoxia, and multidrug resistance proteins.

RESULTS

Twenty newly diagnosed patients [nine primitive neuroectodermal tumors/MBL, one choroid plexus carcinoma, eight malignant gliomas, and two anaplastic ependymomas] were treated. Ten patients, who required neuraxis irradiation, constituted the "PNET" group. These demonstrated five complete and one partial response (PR), with an estimated median progression free survival of 44 months and median survival in excess of 53 months. Patients treated with involved field irradiation were designated the "Glioma" group. Induction chemotherapy produced partial and minor responses (MRs) among 5/10. Their estimated median progression free survival was 6.9 months (P = 0.035 relative to the PNET) with a median survival of 10.7 months (P = 0.04). Age, labeling index, the presence of hypoxia, and Pgp/MDR1 expression failed to discriminate between the two groups.

CONCLUSIONS

This induction regimen produced a cytoreductive response in 6/10 and achieved a significant improvement in progression free survival among 7/10 in the PNET group. Unfortunately, responses among Glioma patients did not translate into durable control. Expression of the biologic factors was similar between both groups and did not correlate with diagnosis or response.

摘要

背景

以下因素已被证明可预测小儿脑肿瘤治疗过程中的疾病进展(PDOT):肿瘤面积>1.5平方厘米且无法切除、胶质母细胞瘤、幕上原始神经外胚层肿瘤以及转移性髓母细胞瘤(MBL)。这项初步研究旨在将肿瘤细胞减灭反应与无进展生存期相关联。

程序

在超分割放疗(RT)之前,先进行四个疗程的顺铂、环磷酰胺、依托泊苷和长春新碱治疗。维持化疗包括八个疗程的卡铂、依托泊苷和长春新碱。对活检标本进行免疫组织化学研究,以检测标记指数、缺氧情况和多药耐药蛋白。

结果

对20例新诊断患者[9例原始神经外胚层肿瘤/MBL患者、1例脉络丛癌患者、8例恶性胶质瘤患者和2例间变性室管膜瘤患者]进行了治疗。10例需要全脑全脊髓照射的患者组成“PNET”组。这些患者中有5例完全缓解,1例部分缓解(PR),估计无进展生存期的中位数为44个月,中位生存期超过53个月。接受累及野照射的患者被指定为“胶质瘤”组。诱导化疗使10例患者中的5例出现部分缓解和轻微缓解(MR)。他们估计的无进展生存期中位数为6.9个月(相对于PNET组,P = 0.035),中位生存期为10.7个月(P = 0.04)。年龄、标记指数、缺氧情况以及Pgp/MDR1表达未能区分这两组患者。

结论

这种诱导方案在10例患者中的6例产生了肿瘤细胞减灭反应,并使PNET组10例患者中的7例无进展生存期有显著改善。不幸的是,胶质瘤患者的缓解并未转化为持久的病情控制。两组患者生物学因素的表达相似,且与诊断或反应无关。

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