Conill Carlos, Jorcano Sandra, Domingo-Doménech Josep, Gallego Rosa, Malvehy Josep, Puig Susana, Sánchez Marcelo, Vilella Ramón, Castel Teresa
Department of Radiation Oncology, Hospital Clinic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
Clin Transl Oncol. 2006 Apr;8(4):266-70. doi: 10.1007/BF02664937.
Whole brain irradiation (WBRT) remains a recommended treatment for patients with brain metastases from malignant melanoma in terms of symptom palliation, especially when extracranial systemic disease is present. Temozolomide (TMZ) has shown efficacy in the treatment of metastatic melanoma. The objective was to evaluate the potential benefit in survival of two different schedules of total dose and fractionation (20 Gy/5 fractions vs 30 Gy/10 fractions) and further TMZ based chemotherapy.
We have conducted a retrospective study in a group of twenty-one patients (RTOG Recursive Partitioning Analysis class II) of the use of WBRT with 20 Gy/5 fractions (n = 11) and 30 Gy/10 fractions (n = 10). All patients received further TMZ based chemotherapy administered as a single chemotherapeutic agent or in combination with chemo-immunotherapy.
Prognostic variables such as: age, Karnofsky performance status, extracranial metastases and number of brain metastases, were analyzed in both groups of treatment without statistically significant differences. The median survival time (MST) for WBRT 20 Gy group was 4 months (CI 95%: range 2- 6 months) and for WBRT 30 Gy group was 4 months (CI 95%: range 0-7 months) without statistically significant differences (Log rank p = 0.74). There was one complete response and two partial responses.
The results suggest that MST was not significantly affected by the total dose/fractionation schedule.
全脑照射(WBRT)仍然是恶性黑色素瘤脑转移患者缓解症状的推荐治疗方法,特别是在存在颅外系统性疾病的情况下。替莫唑胺(TMZ)已显示出对转移性黑色素瘤的治疗效果。目的是评估两种不同总剂量和分割方案(20 Gy/5次分割与30 Gy/10次分割)以及进一步基于TMZ的化疗对生存的潜在益处。
我们对一组21例患者(RTOG递归分区分析II级)进行了一项回顾性研究,这些患者使用了20 Gy/5次分割(n = 11)和30 Gy/10次分割(n = 10)的WBRT。所有患者均接受了进一步基于TMZ的化疗,作为单一化疗药物或与化疗免疫疗法联合使用。
对两组治疗中的年龄、卡诺夫斯基表现状态、颅外转移和脑转移数量等预后变量进行了分析,无统计学显著差异。WBRT 20 Gy组的中位生存时间(MST)为4个月(95%CI:范围2 - 6个月),WBRT 30 Gy组为4个月(95%CI:范围0 - 7个月),无统计学显著差异(对数秩检验p = 0.74)。有1例完全缓解和2例部分缓解。
结果表明,MST不受总剂量/分割方案的显著影响。