Duke University, Durham, NC.
J Oncol Pract. 2018 Jan;14(1):23-31. doi: 10.1200/JOP.2017.026500.
Metastatic lung cancer has long been considered incurable, with the goal of treatment being palliation. However, a clinically meaningful number of these patients with limited metastases (approximately 25%) are living long term after definitive treatment to all sites of active disease. These patients with so-called oligometastatic disease likely represent a distinct clinical group who may possess a more indolent biology compared with their more widely metastatic counterparts. Hellman and Weichselbaum proposed the existence of the oligometastatic state, on the basis of the spectrum theory of cancer spread. The literature suggests that an oligometastatic state exists in patients with non-small-cell lung cancer (NSCLC). This observation in the setting of rapidly evolving systemic therapies, including immune checkpoint inhibitors and an increasing number of targeted therapies, represents a unique clinical opportunity. Metastasis-directed therapies to address sites of disease include surgery (metastasectomy) and/or radiation therapy. Available evidence suggests that treating patients with limited or oligometastases may improve outcomes in a meaningful way; however, the majority of the randomized data includes patients with intracranial metastatic disease, and there are limited robust, randomized data available in the setting of NSCLC with only extracranial sites of metastatic disease. Ongoing randomized trials, including NRG-LU002 and the UK Conventional Care Versus Radioablation (Stereotactic Body Radiotherapy) for Extracranial Oligometastases trial, are aimed at evaluating this question further. One of the current limitations of aggressive treatment of oligometastatic NSCLC is the inability to accurately identify these patients before therapy, yet molecular markers, including microRNA profiles, are being investigated as a promising way to identify these patients.
转移性肺癌长期以来被认为是无法治愈的,治疗的目的是缓解症状。然而,在对所有活跃疾病部位进行明确治疗后,相当数量的局限性转移(约 25%)的这些患者能够长期存活。这些所谓的寡转移疾病患者可能代表了一个独特的临床群体,与广泛转移的患者相比,他们可能具有更惰性的生物学特性。Hellman 和 Weichselbaum 基于癌症扩散的谱理论提出了寡转移状态的存在。文献表明,非小细胞肺癌(NSCLC)患者中存在寡转移状态。在快速发展的全身治疗(包括免疫检查点抑制剂和越来越多的靶向治疗)的背景下观察到这一点,代表了一个独特的临床机会。针对疾病部位的转移定向治疗包括手术(转移切除术)和/或放射治疗。现有证据表明,以有针对性的方式治疗局限性或寡转移患者可能会显著改善患者的预后;然而,大多数随机数据包括有颅内转移的患者,并且在仅有颅外转移部位的 NSCLC 中,只有有限的强有力的随机数据可用。正在进行的随机试验,包括 NRG-LU002 和英国常规护理与放射消融(立体定向体部放射治疗)治疗颅外寡转移瘤试验,旨在进一步评估这个问题。目前,对寡转移 NSCLC 进行积极治疗的一个局限性是在治疗前无法准确识别这些患者,然而,包括 microRNA 谱在内的分子标志物正在被作为一种有前途的识别这些患者的方法进行研究。