Phase 2 Trial of Temozolomide Using Protracted Low-dose and Whole-brain Radiotherapy for Nonsmall Cell Lung Cancer and Breast Cancer Patients With Brain Metastases

被引:120
作者
Addeo, Raffaele [1 ]
De Rosa, Carmine [2 ]
Faiola, Vincenzo [1 ]
Leo, Luigi [3 ]
Cennamo, Gregorio [1 ]
Montella, Liliana [1 ]
Guarrasi, Rosario [1 ]
Vincenzi, Bruno [4 ]
Caraglia, Michele [5 ]
Del Prete, Salvatore [1 ]
机构
[1] S Giovanni Dio Hosp, Oncol Unit, I-80028 Naples, Italy
[2] San Giovanni Bosco Hosp, Neurosurg Unit, Naples, Italy
[3] Hosp Piedimonte Matese, Day Hosp, Oncol Unit, Caserta, Italy
[4] Biomed Univ, Sect Oncol, Rome, Italy
[5] Univ Naples 2, Dept Biochem & Biophys, Naples, Italy
关键词
brain metastases; metronomic therapy; temozolomide; whole-brain radiotherapy;
D O I
10.1002/cncr.23859
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
BACKGROUND. Temozolomide (TMZ), an oral methylating imidazotetrazinone, has antitumor activity against gliomas, malignant melanomas, and brain metastasis and is presently administered as a 5-day oral schedule every 4 weeks. METHODS. A single-institution phase 2 clinical trial was conducted to determine the efficacy and the safety profile of a new regimen based on a dose-intensified, protracted course of TMZ after whole-brain radiotherapy (TRT). Patients were eligible if they had at least 1 bidimensionally measurable brain metastasis from breast cancer and nonsmall cell lung cancer (NSCLC). Twenty-seven patients were treated with 30 grays (Gy) of WBRT with concomitant TMZ (75 mg/m(2)/day) for 10 days, and subsequent TMZ at a dose of 75 mg/m(2) per day for 21 days every 4 weeks, for Lip to 12 cycles. RESULTS. Two complete responses (7.4%) and 11 partial responses (40.7%) were achieved. The schedule appeared to be well tolerated, with grade 3 toxicity (graded according to National Cancer Institute Common Toxicity Criteria) observed in only 2 patients. The overall median survival was 8.8 months and the median progression-free survival was 6 months. CONCLUSIONS. The concomitant use of WBRT and protracted low-dose TMZ appears to be an active, well-tolerated regimen. The observed antitumor activity suggests the need for further investigation of this schedule in combination with other anticancer agents for the concomitant treatment of brain metastases and primary cancers. Cancer 2008; 113:2524-31. (C) 2008 American Cancer Society.
引用
收藏
页码:2524 / 2531
页数:8
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