Yegya-Raman Nikhil, Aisner Joseph, Kim Sinae, Sayan Mutlay, Li Diana, Langenfeld John, Patel Malini, Malhotra Jyoti, Jabbour Salma K
Department of Radiation Oncology, Rutgers Cancer Institute of New Jersey, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, New Jersey.
Division of Medical Oncology, Rutgers Cancer Institute of New Jersey, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, New Jersey.
Adv Radiat Oncol. 2019 Mar 22;4(3):541-550. doi: 10.1016/j.adro.2019.03.005. eCollection 2019 Jul-Sep.
We examined long-term clinical outcomes among patients with synchronous oligometastatic non-small cell lung cancer (NSCLC) treated at our institution with definitive thoracic chemoradiation therapy (CRT) and local therapy to all oligometastatic lesions.
A retrospective review identified 38 patients with synchronous oligometastatic NSCLC (≤3 metastatic lesions) who were treated with definitive CRT to the primary tumor and regional lymph nodes between 1999 and 2017 at our institution. Of the 38 patients, 27 patients (71%) received induction chemotherapy, all of whom responded or stabilized with initial systemic therapy before consideration of CRT. Most patients received chemotherapy concurrently with radiation therapy (n = 32; 84%) and local therapy to the metastatic disease site(s) (n = 34; 89%). We assessed patterns of progression or failure, overall survival (OS), progression-free survival (PFS), and toxicities.
The median follow-up duration was 54.9 months. Most patients (84%) presented with N2 to N3 disease. The brain or central nervous system was the most common site of disease progression and occurred in 16 of 28 patients (57%) experiencing any progression and 10 of 16 patients (63%) who initially presented with brain oligometastases. Median OS was 21.1 months (95% confidence interval [CI], 15.6-49.0 months), and median PFS 9.7 months (95% CI, 8.2-14.4 months). The 1-, 2-, and 4-year OS rates were 75.7%, 45.0%, and 33.7%, respectively. On multivariate analysis, both locoregional progression (hazard ratio: 5.8; 95% CI, 2.2-15.0; = .0003) and distant progression (hazard ratio: 6.0; 95% CI, 2.3-15.4; = .0002), when treated as time-dependent covariates, were associated with inferior OS. Grade ≥3 esophagitis occurred in 9% and grade ≥3 pneumonitis in 5% of patients with evaluable data.
Patients with synchronous oligometastatic NSCLC and a high regional nodal burden treated with definitive thoracic CRT experienced favorable survival outcomes and low toxicity. At our institution, treating oligometastatic disease with CRT after systemic therapy is incorporated into the treatment plan from the onset of therapy, and we monitor the neuraxis closely for progression during and after treatment. Future research should focus on novel treatment combinations, such as immunotherapy or targeted systemic therapy as appropriate to further improve tumor control and survival.
我们研究了在本院接受确定性胸部放化疗(CRT)及对所有寡转移病灶进行局部治疗的同步寡转移非小细胞肺癌(NSCLC)患者的长期临床结局。
一项回顾性研究确定了38例同步寡转移NSCLC(转移灶≤3个)患者,他们于1999年至2017年在本院接受了针对原发肿瘤和区域淋巴结的确定性CRT治疗。在这38例患者中,27例(71%)接受了诱导化疗,所有这些患者在考虑CRT之前,初始全身治疗均有反应或病情稳定。大多数患者在放疗时同时接受化疗(n = 32;84%),并对转移病灶部位进行局部治疗(n = 34;89%)。我们评估了疾病进展或失败模式、总生存期(OS)、无进展生存期(PFS)和毒性反应。
中位随访时间为54.9个月。大多数患者(84%)表现为N2至N3期疾病。脑或中枢神经系统是最常见的疾病进展部位,在28例出现任何进展的患者中有16例(57%),在最初表现为脑寡转移的16例患者中有10例(63%)。中位OS为21.1个月(95%置信区间[CI],15.6 - 49.0个月),中位PFS为9.7个月(95%CI,8.2 - 14.4个月)。1年、2年和4年OS率分别为75.7%、45.0%和33.7%。多因素分析显示,当将局部区域进展(风险比:5.8;95%CI,2.2 - 15.0;P = 0.0003)和远处进展(风险比:6.0;95%CI,2.3 - 15.4;P = 0.0002)作为时间依赖性协变量处理时,均与较差的OS相关。在有可评估数据的患者中,9%发生≥3级食管炎,5%发生≥3级肺炎。
接受确定性胸部CRT治疗的同步寡转移NSCLC且区域淋巴结负荷高的患者生存结局良好且毒性低。在本院,从治疗开始就将全身治疗后用CRT治疗寡转移疾病纳入治疗计划,并且在治疗期间和治疗后密切监测神经轴是否进展。未来的研究应聚焦于新型治疗组合,如适当的免疫治疗或靶向全身治疗,以进一步改善肿瘤控制和生存情况。