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Proposing synchronous oligometastatic non–small‐cell lung cancer based on progression after first‐line systemic therapy

机译:在一线全身疗法后提出基于进展的同步寡粒子非小细胞肺癌

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摘要

Despite the importance of accurate disease definitions for effective management and treatment decisions, there is currently no consensus on what constitutes oligometastatic non–small‐cell lung cancer (NSCLC). Predominant patterns of initial progressive disease (PD) after first‐line systemic therapy have been shown to be a substantial basis for local ablative therapy (LAT) for all disease sites in patients with oligometastatic NSCLC, suggesting that these patterns could be helpful in defining synchronous oligometastatic NSCLC. Therefore, this retrospective study aimed to propose a threshold number of metastases for synchronous oligometastatic NSCLC, based on the pattern of initial PD after first‐line systemic therapy. The cut‐off threshold number of metastases compatible with synchronous oligometastatic NSCLC was determined using receiver operating characteristic (ROC) curve analyses of PD at the initially involved sites alone. ROC analysis of 175 patients revealed that the presence of 1‐3 metastases before first‐line treatment (sensitivity, 85.9%; specificity, 97.3%; area under the curve, 0.91) was compatible with oligometastatic NSCLC, therefore we divided patients into oligometastatic NSCLC and non‐oligometastatic NSCLC groups. Multivariate logistic regression analyses revealed oligometastatic NSCLC to be the only independent predictor of PD at initially involved sites alone (odds ratio 165.7; P < .001). The median survival times in patients with oligometastatic or non‐oligometastatic NSCLC were 23.0 and 10.9 mo (hazard ratio, 0.51; P = .002), respectively. Based on these findings, we propose synchronous oligometastatic NSCLC as 1‐3 metastases in accordance with patterns of initial progression. The result of our study might be contributory to provide a common definition of synchronous oligometastatic NSCLC.
机译:尽管准确的疾病定义对于有效的管理和治疗决策具有重要性,但目前没有关于构成寡核桃瘤非小细胞肺癌(NSCLC)的共识。初始渐进性疾病(PD)的主要模式已被证明是寡核素患者患者患者局部消融治疗(LAT)的主要基础,表明这些模式可能有助于定义同步寡矩形NSCLC。因此,该回顾性研究旨在提出基于首次全身治疗后初始PD的图案的同步寡粒状NSCLC的阈值数量的转移。使用在最初涉及的位点在最初涉及的位点处,使用接收器操作特性(ROC)曲线分析来确定与同步寡素塑料NSCLC兼容的转移截止阈值数。 175名患者的ROC分析表明,一线治疗前1-3种转移(敏感性,85.9%;特异性,97.3%;曲线下的面积为0.91)与寡素塑料NSCLC相容,因此我们将患者分为寡核桃素NSCLC和非寡粒子素的NSCLC基团。多变量逻辑回归分析显示寡矩形NSCLC是最初涉及单独涉及的位点的Pd的唯一独立预测因子(差距165.7; p <.001)。寡矩形或非寡粒子患者的中位存活时间分别为23.0和10.9Mo(危害比,0.51; p = .002)。基于这些发现,我们根据初始进展的模式提出了同步的寡素球阀作为1-3转移率。我们研究的结果可能是提供同步寡粒子塑料NSCLC的共同定义的贡献。

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