Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Cancer. 2020 Oct 15;126(20):4572-4583. doi: 10.1002/cncr.33109. Epub 2020 Jul 30.
Progressive, metastatic non-small cell lung cancer (NSCLC) often requires the initiation of new systemic therapy. However, in patients with NSCLC that is oligoprogressive (≤3 lesions), local radiotherapy (RT) may allow for the eradication of resistant microclones and, therefore, the continuation of otherwise effective systemic therapy.
Patients treated from 2008 to 2019 with definitive doses of RT to all sites of intracranial or extracranial oligoprogression without a change in systemic therapy were identified. Radiographic progression-free survival (rPFS) and time to new therapy (TNT) were measured. Associations between baseline clinical and treatment-related variables were correlated with progression-free survival via Cox proportional hazards modeling.
Among 198 unique patients, 253 oligoprogressive events were identified. Intracranial progression occurred in 51% of the patients, and extracranial progression occurred in 49%. In the entire cohort, the median rPFS was 7.9 months (95% CI, 6.5-10.0 months), and the median TNT was 8.8 months (95% CI, 7.2-10.9 months). On adjusted modeling, patients with the following disease characteristics were associated with better rPFS: better performance status (P = .003), fewer metastases (P = .03), longer time to oligoprogression (P = .009), and fewer previous systemic therapies (P = .02). Having multiple sites of oligoprogression was associated with worse rPFS (P < .001).
In select patients with oligoprogression, definitive RT is a feasible treatment option to delay the initiation of next-line systemic therapies, which have more limited response rates and efficacy. Further randomized prospective data may help to validate these findings and identify which patients are most likely to benefit.
进展性、转移性非小细胞肺癌(NSCLC)常需要开始新的全身治疗。然而,在寡进展(≤3 个病灶)的 NSCLC 患者中,局部放疗(RT)可能能够根除耐药微克隆,从而继续进行有效的全身治疗。
本研究纳入了自 2008 年至 2019 年期间,接受过全脑或颅外寡进展部位根治剂量放疗且未改变全身治疗的患者。测量了影像学无进展生存期(rPFS)和新治疗时间(TNT)。通过 Cox 比例风险模型,将基线临床和治疗相关变量与无进展生存相关联。
在 198 名患者中,共识别出 253 例寡进展事件。颅内进展发生于 51%的患者,颅外进展发生于 49%的患者。在整个队列中,中位 rPFS 为 7.9 个月(95%CI,6.5-10.0 个月),中位 TNT 为 8.8 个月(95%CI,7.2-10.9 个月)。在调整后的模型中,具有以下疾病特征的患者 rPFS 较好:较好的体能状态(P=0.003)、转移灶较少(P=0.03)、寡进展时间较长(P=0.009)、以及接受过的全身治疗较少(P=0.02)。有多个部位寡进展与 rPFS 较差相关(P<0.001)。
在选择的寡进展患者中,根治性 RT 是一种可行的治疗选择,可以延迟下一阶段全身治疗的开始,后者的缓解率和疗效有限。进一步的随机前瞻性数据可能有助于验证这些发现,并确定哪些患者最有可能受益。