Langston Jacob, Patil Tejas, Ross Camidge D, Bunn Paul A, Schenk Erin L, Pacheco Jose M, Jurica James, Waxweiler Timothy V, Kavanagh Brian D, Rusthoven Chad G
University of Colorado School of Medicine, Department of Radiation Oncology, USA.
University of Colorado School of Medicine, Division of Medical Oncology, Department of Medicine, USA.
Lung Cancer. 2023 Apr;178:103-107. doi: 10.1016/j.lungcan.2023.02.006. Epub 2023 Feb 8.
For extensive brain metastases (BrM) presentations arising from oncogene-addicted lung cancer, tyrosine kinase inhibitors (TKIs) with high response rates in the central nervous system (CNS) could potentially downstage the CNS disease burden, allowing for the avoidance of upfront whole-brain radiotherapy (WBRT) and the conversion of some patients into candidates for focal stereotactic radiosurgery (SRS).
We describe the outcomes of patients with ALK, EGFR, and ROS1-driven NSCLC with extensive BrM presentations (defined as > 10 BrMs or leptomeningeal disease) treated with upfront newer generation CNS-active TKIs alone, including osimertinib, alectinib, brigatinib, lorlatinib, and entrectinib, from 2012 to 2021 at our institution. All BrMs were contoured at study entry, best CNS response (nadir), and first CNS progression.
Twelve patients met criteria including 6 with ALK, 3 with EGFR, and 3 with ROS1-driven NSCLC. The median number and volume of BrMs at presentation were 49 and 19.6 cm, respectively. Eleven patients (91.7 %) achieved a CNS response by modified-RECIST criteria to upfront TKI (10 partial responses, 1 complete response, 1 stable disease) with nadir observed at a median of 5.1 months. At nadir, the median number and volume of BrMs were 5 (median 91.7 % reduction per-patient) and 0.3 cm(median 96.5 % reduction per-patient), respectively. Eleven patients (91.6 %) developed subsequent CNS progression (7 local failures, 3 local + distant, 1 distant) at a median of 17.9 months. At CNS progression, the median number and volume of BrMs were 7 and 0.7 cm, respectively. Seven patients (58.3 %) received salvage SRS and no patients received salvage WBRT. The median overall survival from initiation of TKI for the extensive BrM presentation was 43.2 months.
In this initial case series, we describe CNS downstaging as a promising multidisciplinary treatment paradigm involving the upfront administration CNS-active systemic therapy and close MRI surveillance for extensive BrMs as a strategy to avoid upfront WBRT and to convert some patients into SRS candidates.
对于由致癌基因成瘾性肺癌引起的广泛脑转移(BrM)表现,在中枢神经系统(CNS)中具有高缓解率的酪氨酸激酶抑制剂(TKIs)可能会降低CNS疾病负担,从而避免 upfront 全脑放疗(WBRT),并使一些患者转变为适用于局灶性立体定向放射外科治疗(SRS)的候选人。
我们描述了2012年至2021年在我们机构接受 upfront 新一代中枢神经系统活性TKIs单独治疗的ALK、EGFR和ROS1驱动的非小细胞肺癌(NSCLC)且伴有广泛BrM表现(定义为>10个BrM或软脑膜疾病)患者的结局。所有BrM在研究入组时、最佳CNS缓解(最低点)和首次CNS进展时进行轮廓勾画。
12名患者符合标准,包括6名ALK驱动、3名EGFR驱动和3名ROS1驱动的NSCLC患者。就诊时BrM的中位数数量和体积分别为49个和19.6 cm。11名患者(91.7%)根据改良RECIST标准对 upfront TKI达到CNS缓解(10例部分缓解,1例完全缓解,1例疾病稳定),最低点出现在中位时间5.1个月。在最低点时,BrM的中位数数量和体积分别为5个(每位患者中位数减少91.7%)和0.3 cm(每位患者中位数减少96.5%)。11名患者(91.6%)随后出现CNS进展(7例局部失败,3例局部+远处,1例远处),中位时间为17.9个月。在CNS进展时,BrM的中位数数量和体积分别为7个和0.7 cm。7名患者(58.3%)接受了挽救性SRS,无患者接受挽救性WBRT。对于广泛BrM表现,从开始使用TKI起的中位总生存期为43.2个月。
在这个初始病例系列中,我们将CNS降期描述为一种有前景的多学科治疗模式,包括 upfront 给予中枢神经系统活性全身治疗以及对广泛BrM进行密切的MRI监测,作为避免 upfront WBRT并使一些患者转变为SRS候选人的策略。