Minniti Giuseppe, Scaringi Claudia, Lanzetta Gaetano, Bozzao Alessandro, Romano Andrea, De Sanctis Vitaliana, Valeriani Maurizio, Osti Mattia, Enrici Riccardo Maurizi
Unit of Radiation Oncology, Sant'Andrea Hospital, University Sapienza, Via di Grottarossa 1035, 00189, Rome, Italy.
IRCCS Neuromed, 86077, Pozzilli, IS, Italy.
J Neurooncol. 2014 Jun;118(2):329-334. doi: 10.1007/s11060-014-1435-0. Epub 2014 Apr 10.
A second course of whole brain radiation therapy (WBRT) has been employed in selected patients with progressive brain metastases providing favorable symptomatic palliation with acceptable toxicity, although its efficacy and safety remain matter of debate. In the present study we have evaluated the outcomes in patients with progressive intracranial disease treated with WBRT reirradiation and concurrent temozolomide between October 2010 and May 2013. Data were obtained from a prospectively maintained database including patients with brain tumors treated with radiotherapy at Sant'Andrea Hospital. We identified 27 patients (10 males and 17 females) with a median age of 54 years who received WBRT reirradiation at a dose of 25 Gy in ten fractions plus concomitant daily temozolomide administered orally at a dose of 75 mg/m(2). At the time of repeat WBRT all patients had a KPS ≥ 60. The primary disease sites were lung (n = 18) and breast (n = 9). The median overall survival after the second course of WBRT was 6.2 months and the median time to progression was 5.5 months. Eight patients experienced complete resolution of symptoms, 9 patients had a significant improvement, and 6 patients had no change in their neurologic function. Four patients had further deterioration after reirradiation. Overall, 85 % of patients improved or maintained their neurologic status. No severe acute toxicity during or after the second course of WBRT reirradiation was observed. On multivariate analysis with the Cox proportional hazards model, stable or absent extracranial metastases (p = 0.005) and response to treatment (p = 0.01) were independent favorable prognostic factors for survival. The median and 12-month survival rates were 12 months and 50 % in patients with stable or absent extracranial disease and 4.6 months and 7 % in those with progressive extracranial disease (p = 0.001). In conclusion, in the respect to the small number of treated patients, repeat WBRT plus concomitant temozolomide may be a treatment option in selected patients with multiple brain metastases to improve or maintain neurological conditions and quality of life with acceptable toxicity. The favorable effects of concomitant temozolomide on survival remain unclear.
对于部分脑转移进展患者,已采用第二疗程的全脑放射治疗(WBRT),其能提供良好的症状缓解且毒性可接受,尽管其疗效和安全性仍存在争议。在本研究中,我们评估了2010年10月至2013年5月期间接受WBRT再照射及同步替莫唑胺治疗的颅内疾病进展患者的预后。数据来自前瞻性维护的数据库,该数据库包括在圣安德烈亚医院接受放射治疗的脑肿瘤患者。我们确定了27例患者(10例男性和17例女性),中位年龄54岁,接受了剂量为25 Gy分10次的WBRT再照射,同时每日口服剂量为75 mg/m²的替莫唑胺。在重复WBRT时,所有患者的KPS≥60。原发疾病部位为肺(n = 18)和乳腺(n = 9)。第二疗程WBRT后的中位总生存期为6.2个月,中位疾病进展时间为5.5个月。8例患者症状完全缓解,9例患者有显著改善,6例患者神经功能无变化。4例患者再照射后病情进一步恶化。总体而言,85%的患者神经状态得到改善或维持。在第二疗程WBRT再照射期间或之后未观察到严重急性毒性。使用Cox比例风险模型进行多因素分析时,颅外转移稳定或无转移(p = 0.005)和对治疗的反应(p = 0.01)是生存的独立有利预后因素。颅外疾病稳定或无转移患者的中位生存期和12个月生存率分别为12个月和50%,颅外疾病进展患者分别为4.6个月和7%(p = 0.001)。总之,鉴于治疗患者数量较少,重复WBRT加同步替莫唑胺可能是部分多发脑转移患者改善或维持神经状况及生活质量且毒性可接受的一种治疗选择。同步替莫唑胺对生存的有利影响仍不清楚。