Chen Yuxian, Li Yang, Meng Hong, Li Chunhai, Kong Fanlei
Department of Radiology, Qilu Hospital of Shandong University, Jinan, China.
Department of Medical Oncology, The People's Hospital of Zouping City, Binzhou, China.
Front Oncol. 2024 Oct 7;14:1445245. doi: 10.3389/fonc.2024.1445245. eCollection 2024.
To evaluate the safety and efficacy of microwave ablation (MWA) for high-risk pulmonary nodules in patients infected with the Omicron variant within 3 months, a retrospective study was conducted.
The study included patients with multiple high-risk nodules who underwent CT-guided MWA from April 2022 to April 2023. Patients were divided into an observation group and a control group. The primary endpoints were postoperative complications and hospital length of stay, while the secondary endpoint was progression-free survival (PFS).
A total of 157 patients were included in the analysis, with 64 in the observation group and 93 in the control group. No deaths occurred within 30 days after MWA. In the observation group, the median follow-up time was 7 months, during which 5 patients experienced disease progression after MWA, including 3 cases of pulmonary metastases. Complications were primarily pneumothorax, pleural effusion, and hemorrhage, with an incidence rate of 57.8%, which was statistically significant (p=0.005). The median length of hospital stay was 5 days for the observation group and 6 days for the control group. There was no statistically significant difference in PFS between the two groups after the removal of lung metastases (p=0.265).
CT-guided MWA is an alternative treatment for patients with high-risk lung nodules who have been infected with Omicron within the past 3 months.
为评估微波消融(MWA)对3个月内感染奥密克戎变异株患者的高危肺结节的安全性和有效性,进行了一项回顾性研究。
该研究纳入了2022年4月至2023年4月期间接受CT引导下MWA的多发高危结节患者。患者分为观察组和对照组。主要终点为术后并发症和住院时间,次要终点为无进展生存期(PFS)。
共有157例患者纳入分析,观察组64例,对照组93例。MWA后30天内无死亡病例。观察组中位随访时间为7个月,期间5例患者MWA后出现疾病进展,其中3例发生肺转移。并发症主要为气胸、胸腔积液和出血,发生率为57.8%,差异有统计学意义(p=0.005)。观察组中位住院时间为5天,对照组为6天。去除肺转移灶后两组PFS差异无统计学意义(p=0.265)。
CT引导下MWA是过去3个月内感染奥密克戎的高危肺结节患者的一种替代治疗方法。