Doherty Mark K, Korpanty Grzegorz J, Tomasini Pascale, Alizadeh Moein, Jao Kevin, Labbé Catherine, Mascaux Celine M, Martin Petra, Kamel-Reid Suzanne, Tsao Ming-Sound, Pintilie Melania, Liu Geoffrey, Bradbury Penelope A, Feld Ronald, Leighl Natasha B, Chung Caroline, Shepherd Frances A
Department of Medical Oncology, Princess Margaret Cancer Centre, Toronto, Canada.
Department of Medical Oncology, Princess Margaret Cancer Centre, Toronto, Canada.
Radiother Oncol. 2017 May;123(2):195-202. doi: 10.1016/j.radonc.2017.03.007. Epub 2017 Mar 28.
Brain metastases in EGFR/ALK-driven NSCLC frequently pose treatment dilemmas. Tyrosine kinase inhibitors (TKIs) can control extracranial disease, but radiotherapy is often required for intracranial control. We aimed to evaluate the impact of first-line whole brain radiotherapy (WBRT), stereotactic radiotherapy (SRS) or TKI alone on outcomes of patients with brain metastases from EGFR/ALK-driven NSCLC.
This single center retrospective review included 184 patients with brain metastases from EGFR/ALK-driven NSCLC, and analyzed effect of treatment choice on time to intracranial progression (TTIP) and overall survival (OS).
First-line treatment for brain metastases consisted of WBRT in 120 patients, SRS in 37 and TKI alone in 27. WBRT-treated patients had more brain metastases, and more baseline symptoms. Median TTIP was longer in the WBRT group at 50.5months than SRS or TKI groups at 12 and 15months (p=0.0038). No significant difference was seen in median OS: 21.6months in the WBRT group, 23.9months in the SRS group and 22.6months in the TKI group (p=0.67). In multivariable analysis, age>65years (HR 2.2, p=0.0014), greater number of brain metastases (HR 2.48, p=0.0002) and greater number of extracranial metastatic sites (2 vs 0-1 HR=2.05, p=0.014 and 3+ vs 0-1 HR=2.95, p=0.0001 were associated with shorter OS. No independent effect was seen from first-line CNS treatment choice.
First-line WBRT for brain metastases from EGFR/ALK-driven NSCLC was associated with longer TTIP than SRS or TKI alone, with no difference in OS. These results could support deferral of WBRT until intracranial progression in selected patients who are closely monitored.
表皮生长因子受体(EGFR)/间变性淋巴瘤激酶(ALK)驱动的非小细胞肺癌(NSCLC)脑转移常常带来治疗难题。酪氨酸激酶抑制剂(TKIs)可控制颅外疾病,但颅内控制通常需要放疗。我们旨在评估一线全脑放疗(WBRT)、立体定向放疗(SRS)或单纯TKI对EGFR/ALK驱动的NSCLC脑转移患者预后的影响。
这项单中心回顾性研究纳入了184例EGFR/ALK驱动的NSCLC脑转移患者,分析了治疗选择对颅内进展时间(TTIP)和总生存期(OS)的影响。
脑转移的一线治疗包括120例患者接受WBRT,37例接受SRS,27例单纯接受TKI。接受WBRT治疗的患者脑转移更多,基线症状也更多。WBRT组的中位TTIP为50.5个月,长于SRS组的12个月和TKI组的15个月(p = 0.0038)。中位OS无显著差异:WBRT组为21.6个月,SRS组为23.9个月,TKI组为22.6个月(p = 0.67)。在多变量分析中,年龄>65岁(HR 2.2,p = 0.0014)、脑转移数量更多(HR 2.48,p = 0.0002)和颅外转移部位数量更多(2个vs 0 - 1个HR = 2.05,p = 0.014;3个及以上vs 0 - 1个HR = 2.95,p = 0.0001)与较短的OS相关。一线中枢神经系统治疗选择未显示出独立影响。
EGFR/ALK驱动的NSCLC脑转移一线WBRT与单独使用SRS或TKI相比,TTIP更长,OS无差异。这些结果可能支持在密切监测的特定患者中,将WBRT推迟至颅内进展时使用。