Department of Thoracic Surgery, The Second Xiangya Hospital, Central South University, 139 Middle Renmin Road, Changsha, Hunan, 410013, China.
Xiangya School of Medicine, Central South University, Changsha, 410078, Hunan, China.
J Neurooncol. 2017 Nov;135(2):217-227. doi: 10.1007/s11060-017-2572-z. Epub 2017 Jul 19.
Brain metastasis is the leading cause of death among advanced non-small cell lung cancer (NSCLC) and breast cancer patients. The standard treatment for brain metastases is radiotherapy. The combination of radiotherapy and chemotherapy has been tested. However, the management of brain metastases has yet to be successful. Here, we aimed to determine the efficacy and safety of whole brain radiotherapy (WBRT) alone or in combination with temozolomide (TMZ) in NSCLC and breast cancer patients with brain metastases. A systematic review of PubMed, CNKI (China National Knowledge Infrastructure) and WANFANG (WANGFANG data) involving 870 patients were conducted. Fourteen randomized controlled trials (RCTs) were independently identified by two reviewers. The primary outcome measures were objective response rate (ORR), overall survival (OS), progression-free survival (PFS) and toxicity. The ORR was better with combination therapy of WBRT and TMZ than with WBRT alone (RR = 1.34, p < 0.00001) and subgroup analysis showed a significantly superior ORR in NSCLC patients (RR = 1.38, p < 0.00001), but not in breast cancer patients (RR = 1.03, p = 0.86). OS and PFS did not significantly differ between combination therapy and WBRT alone. A higher rate of toxicity was observed in combination therapy than in WBRT alone (RR = 1.83, p = 0.0006). No advantages of concurrent WBRT and TMZ were observed in breast cancer patients with brain metastases. Combination therapy was associated with improved ORR in NSCLC patients, especially in Chinese patients. As a "surrogate endpoint" for OS, ORR may allow a conclusion to be made about the management of NSCLC with brain metastases with the combination of WBRT and TMZ. However, it needs to be validated to show that improved ORR predicts the treatment effects on the clinical benefit. The ORR may be valid for a particular indication such as status of MGMT promoter methylation.
脑转移是晚期非小细胞肺癌(NSCLC)和乳腺癌患者死亡的主要原因。脑转移的标准治疗是放疗。已经测试了放疗联合化疗。然而,脑转移的治疗尚未成功。在这里,我们旨在确定单纯全脑放疗(WBRT)或联合替莫唑胺(TMZ)治疗 NSCLC 和乳腺癌脑转移患者的疗效和安全性。我们对PubMed、中国知网(CNKI)和万方(WANFANG data)进行了系统评价,共纳入 870 名患者。两名评审员独立识别了 14 项随机对照试验(RCTs)。主要观察指标为客观缓解率(ORR)、总生存期(OS)、无进展生存期(PFS)和毒性。WBRT 联合 TMZ 治疗的 ORR 优于单纯 WBRT(RR=1.34,p<0.00001),亚组分析显示 NSCLC 患者的 ORR 明显更高(RR=1.38,p<0.00001),但乳腺癌患者无明显差异(RR=1.03,p=0.86)。联合治疗与单纯 WBRT 相比,OS 和 PFS 无显著差异。联合治疗的毒性发生率高于单纯 WBRT(RR=1.83,p=0.0006)。联合 WBRT 和 TMZ 治疗对乳腺癌脑转移患者没有优势。联合治疗可提高 NSCLC 患者,尤其是中国患者的 ORR。作为 OS 的“替代终点”,ORR 可能有助于得出 NSCLC 合并脑转移患者采用 WBRT 和 TMZ 联合治疗的结论。然而,需要验证改善的 ORR 是否预测治疗对临床获益的效果。ORR 可能对特定的适应证有效,如 MGMT 启动子甲基化状态。