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替莫唑胺化疗联合同步低分割调强放疗治疗新诊断多形性胶质母细胞瘤的Ⅰ期临床试验

Phase I trial of hypofractionated intensity-modulated radiotherapy with temozolomide chemotherapy for patients with newly diagnosed glioblastoma multiforme.

机构信息

Department of Radiation Oncology, University of Colorado School of Medicine, Aurora, CO 80045, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2011 Nov 15;81(4):1066-74. doi: 10.1016/j.ijrobp.2010.07.021. Epub 2010 Oct 6.

Abstract

PURPOSE

To determine the maximal tolerated biologic dose intensification of radiotherapy using fractional dose escalation with temozolomide (TMZ) chemotherapy in patients with newly diagnosed glioblastoma multiforme.

METHODS AND MATERIALS

Patients with newly diagnosed glioblastoma multiforme after biopsy or resection and with adequate performance status, bone marrow, and organ function were eligible. The patients underwent postoperative intensity-modulated radiotherapy (IMRT) with concurrent and adjuvant TMZ. All patients received a total dose of 60 Gy to the surgical cavity and residual tumor, with a 5-mm margin. IMRT biologic dose intensification was achieved by escalating from 3 Gy/fraction (Level 1) to 6 Gy/fraction (Level 4) in 1-Gy increments. Concurrent TMZ was given at 75 mg/m(2)/d for 28 consecutive days. Adjuvant TMZ was given at 150-200 mg/m(2)/d for 5 days every 28 days. Dose-limiting toxicity was defined as any Common Terminology Criteria for Adverse Events, version 3, Grade 3-4 nonhematologic toxicity, excluding Grade 3 fatigue, nausea, and vomiting. A standard 3+3 Phase I design was used.

RESULTS

A total of 16 patients were accrued (12 men and 4 women, median age, 69 years; range, 34-84. The median Karnofsky performance status was 80 (range, 60-90). Of the 16 patients, 3 each were treated at Levels 1 and 2, 4 at Level 3, and 6 at Level 4. All patients received IMRT and concurrent TMZ according to the protocol, except for 1 patient, who received 14 days of concurrent TMZ. The median number of adjuvant TMZ cycles was 7.5 (range, 0-12). The median survival was 16.2 months (range, 3-33). One patient experienced vision loss in the left eye 7 months after IMRT. Four patients underwent repeat surgery for suspected tumor recurrence 6-12 months after IMRT; 3 had radionecrosis.

CONCLUSIONS

The maximal tolerated IMRT fraction size was not reached in our study. Our results have shown that 60 Gy IMRT delivered in 6-Gy fractions within 2 weeks with concurrent and adjuvant TMZ is tolerable in selected patients with a T(1)-weighted enhancing tumor <6 cm.

摘要

目的

在新诊断的多形性胶质母细胞瘤患者中,通过分次递增剂量联合替莫唑胺(TMZ)化疗,确定放疗的最大耐受生物剂量强化。

方法和材料

活检或切除后且体能状态、骨髓和器官功能良好的新诊断的多形性胶质母细胞瘤患者符合入组条件。所有患者均接受术后强度调制放疗(IMRT),并同时给予 TMZ 化疗及辅助治疗。所有患者均接受 60 Gy 全脑照射,其中 5 Gy 用于手术野和残余肿瘤,边缘扩大 5 mm。通过 1 Gy 递增量,从 3 Gy/分次(1 级)递增至 6 Gy/分次(4 级),实现 IMRT 生物剂量强化。同步 TMZ 剂量为 75 mg/m2/d,连用 28 天。辅助 TMZ 剂量为 150-200 mg/m2/d,每 28 天用 5 天。剂量限制性毒性定义为任何不良事件通用术语标准,第 3 版,3-4 级非血液学毒性,不包括 3 级疲劳、恶心和呕吐。采用标准的 3+3 期 I 设计。

结果

共入组 16 例患者(男 12 例,女 4 例,中位年龄 69 岁,范围 34-84 岁;中位 Karnofsky 体能状态评分为 80 分(范围 60-90 分)。16 例患者中,各有 3 例接受 1 级和 2 级治疗,4 例接受 3 级治疗,6 例接受 4 级治疗。除 1 例患者接受 14 天同步 TMZ 治疗外,其余患者均按方案接受 IMRT 和同步 TMZ 治疗。中位辅助 TMZ 周期数为 7.5 个(范围 0-12 个)。中位生存期为 16.2 个月(范围 3-33 个月)。1 例患者在 IMRT 后 7 个月出现左眼视力丧失。4 例患者在 IMRT 后 6-12 个月因疑似肿瘤复发而再次手术;其中 3 例为放射性坏死。

结论

在本研究中,未达到 IMRT 的最大耐受分次剂量。我们的结果表明,在选择的 T1 加权增强肿瘤<6 cm 的患者中,2 周内给予 6 Gy 分次的 60 Gy IMRT,并同时给予替莫唑胺化疗及辅助治疗是可以耐受的。

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