Wang Feng, Ning Fangling, Liu Changmin, Hao Yanzhang, Li LiMian, Yu Zeshun, Chen Shaoshui, Li Baosheng
Shandong Cancer Hospital, Shandong University, Ji Yan Road No. 440, Jinan, 250117, Shandong, China.
Cell Biochem Biophys. 2015 Mar;71(2):1261-5. doi: 10.1007/s12013-014-0286-9.
The purpose of this study is to compare the efficacy and safety of Gefitinib versus VMP in combination with three-dimensional conformal radiotherapy (3D-CRT) for multiple brain metastases from non-small cell lung cancer (NSCLC). A total of 73 NSCLC patients with brain metastases from January 2010 to August 2013 were randomly divided into Gefitinib group (37 patients) and VMP chemotherapy group (36 patients). Patients in VMP group received VM-26 100 mg/day by intravenous injection, from day 1 to day 3, cisplatin 25 mg/m2 by intravenous injection, from day 1 to day 3. One cycle was defined as a 21-day therapy duration, with a total of 3 cycles; 2 cycles were used for consolidation. Patients in Gefitinib group received Gefitinib orally. Both groups received 3D-CRT, DT50 Gy/25f/35d from first day and target areas were treated with whole brain radiotherapy. The results of the study are listed below: There was no significant difference in the short-term effects of the two groups (P > 0.05). Median survival time (MST) of Gefitinib was 13.3 months whereas median survival time of VMP group is 12.7 months (P < 0.05). In Gefitinib group, we did not observe any difference of the median survival time between the patients with and without mutation EGFR. Toxicity of Gefitinib groups were characterized by rash, whereas chemotherapy resulted in hematologic toxicities, which included 6 cases of III/IV leucopenia (17.6 %), 3 cases of anemia (8.8 %), and 5 cases of thrombocytopenia (14.7 %), and non-hematological toxicity which was less serious symptoms for gastrointestinal disorders, hair loss, etc. These adverse reactions can be released after symptomatic treatment. No treatment-related deaths occurred. Two patients in VMP group quit due to IV leucopenia. Both oral Gefitinib and systemic VMP chemotherapy in combination with three-dimensional conformal radiotherapy (3D-CRT) could be used to treat brain metastases from non-small cell lung cancer. There were no difference in the short-term effects of the two groups, but long-term effect of Gefitinib group was slightly better than VMP group. Moreover, Gefitinib group showed low toxicity. All together, our finding implicated that Gefitinib is an effective method for patients with brain metastases from NSCLC.
本研究旨在比较吉非替尼与长春花碱酰胺和顺铂联合三维适形放疗(3D-CRT)治疗非小细胞肺癌(NSCLC)多发脑转移的疗效和安全性。2010年1月至2013年8月,共73例NSCLC脑转移患者被随机分为吉非替尼组(37例)和长春花碱酰胺和顺铂化疗组(VMP组,36例)。VMP组患者于第1至3天静脉注射长春花碱酰胺100mg/天,第1至3天静脉注射顺铂25mg/m²。一个周期定义为21天的治疗疗程,共3个周期;2个周期用于巩固治疗。吉非替尼组患者口服吉非替尼。两组均接受3D-CRT,从第一天开始DT50Gy/25f/35d,靶区接受全脑放疗。研究结果如下:两组短期疗效无显著差异(P>0.05)。吉非替尼组的中位生存时间(MST)为13.3个月,而VMP组为12.7个月(P<0.05)。在吉非替尼组中,我们未观察到有或无表皮生长因子受体(EGFR)突变患者的中位生存时间有任何差异。吉非替尼组的毒性表现为皮疹,而化疗导致血液学毒性,其中包括6例III/IV级白细胞减少(17.6%)、3例贫血(8.8%)和5例血小板减少(14.7%),非血液学毒性为胃肠道紊乱、脱发等较轻症状。这些不良反应经对症治疗后可缓解。未发生与治疗相关的死亡。VMP组有2例患者因IV级白细胞减少而退出。口服吉非替尼和全身VMP化疗联合三维适形放疗(3D-CRT)均可用于治疗非小细胞肺癌脑转移。两组短期疗效无差异,但吉非替尼组的长期疗效略优于VMP组。此外,吉非替尼组毒性较低。总体而言,我们的研究结果表明吉非替尼是治疗NSCLC脑转移患者的一种有效方法。