Mehta Hiren J, Jantz Michael A
Division of Pulmonary/Critical care/Sleep Medicine, University of Florida College of Medicine;
Division of Pulmonary/Critical care/Sleep Medicine, University of Florida College of Medicine.
J Vis Exp. 2017 Feb 12(120):54855. doi: 10.3791/54855.
Isolated hilar and mediastinal recurrence (IMHR) following external beam radiation therapy (EBRT) in patients with lung cancer is common. These patients do not have many treatment options and are usually offered palliative chemotherapy or best supportive care. Endobronchial ultrasound (EBUS)-guided intratumoral injection of cisplatin (ITC) is a novel approach for these patients. The procedure is performed under conscious sedation. The lesion is located with a bronchoscopy using EBUS, and a 22-gauge EBUS needle is advanced through the working channel of the scope and locked in position. Under ultrasound guidance, the wall of the tracheobronchial tree is punctured and the needle is moved into the target lesion. The needle stylet is then removed and cisplatin (40 mg/40 mL) is injected into the lesion. One to two sites are treated per session. Details of the procedure are described in the protocol section of paper. At our center, 50 sites were treated in 36 patients (19 males, 17 females). The mean age of our cohort was 61.9 ±8.5 years. We performed final analyses on 35 patients and 41 sites. 24/35 (69%) had complete or partial response (responders), whereas 11/35 (31%) had stable or progressive disease (non-responders). Overall, survival in our group was 8 months (95% CI of 6-11 months), with patients who responded having significantly better survival than the ones who did not.
肺癌患者在接受外照射放疗(EBRT)后出现孤立性肺门和纵隔复发(IMHR)很常见。这些患者没有太多治疗选择,通常接受姑息化疗或最佳支持治疗。支气管内超声(EBUS)引导下瘤内注射顺铂(ITC)是针对这些患者的一种新方法。该操作在清醒镇静下进行。使用EBUS通过支气管镜定位病变,将一根22号EBUS针经内镜工作通道推进并锁定在适当位置。在超声引导下,穿刺气管支气管树壁,将针插入目标病变。然后拔出针芯,将顺铂(40mg/40mL)注入病变内。每次治疗1至2个部位。该操作的详细信息在论文的方案部分进行了描述。在我们中心,36例患者(19例男性,17例女性)共治疗了50个部位。我们研究队列的平均年龄为61.9±8.5岁。我们对35例患者和41个部位进行了最终分析。24/35(69%)有完全或部分缓解(缓解者),而11/35(31%)有疾病稳定或进展(无缓解者)。总体而言,我们组的生存期为8个月(95%CI为6至11个月),缓解者的生存期明显优于未缓解者。