Lee B H, Choe D H, Lee J H, Kim K H, Chin S Y
Department of Radiology, Korea Cancer Center Hospital, Seoul, Korea.
AJR Am J Roentgenol. 1997 Mar;168(3):741-5. doi: 10.2214/ajr.168.3.9057527.
The purpose of this prospective study was to evaluate the long-term clinical efficacy of metallic stents when used as the initial palliative treatment of patients with inoperable malignant biliary obstruction.
From August 1991 through May 1995, 100 consecutive patients with malignant biliary obstruction were treated with percutaneous placement of metallic stents. The causes of obstruction were bile duct carcinoma (n = 50), pancreatic carcinoma (n = 17), gallbladder carcinoma (n = 6), hepatocellular carcinoma (n = 2), and metastatic lymphadenopathy in the hepatoduodenal ligament (n = 25). We used 123 stents: 64 Gianturco Z stents, 39 Hanaro spiral stents, 16 Wallstents, two tantalum Strecker stents, one Endocoil stent, and one Memotherm nitinol stent. Every 3 months we followed up all patients except those who died. The average length of follow-up was 220 days (range, 4-1125 days). Patient survival and stent patency rates were estimated by life-table analysis.
The median length of survival for the entire patient group was 246 days: 25-week and 50-week survival rates were 62% and 25%, respectively. We found no statistically significant difference in the median length of survival between patients with hilar obstruction (256 days) and patients with common bile duct (CBD) obstruction (227 days). Patients with bile duct carcinoma had longer median survival (269 days) than did patients with other conditions (197 days). The overall median length of patency for all stents was 360 days; the 25-week and 50-week patency rates were 81% and 53%, respectively. The stent patency rate at the median length of survival was 71%. The median length of stent patency in patients with hilar obstruction (617 days) was nearly double that of patients with CBD obstruction (324 days). However, the median length of stent patency in patients with bile duct carcinoma showed no statistically significant difference from the median length in patients with other disease. Four patients (4%) died within 1 month after stent placement. Twenty-one patients (21%) developed recurrent jaundice or cholangitis. In order of frequency, the causes of recurrent jaundice were tumor overgrowth, incrustation of bile sludge, duodenal obstruction due to tumor invasion, stent impaction into the bile duct wall, stent malposition, and tumor ingrowth.
Metallic stents showed a favorable patency rate with regard to patient survival. In patients with hilar obstruction, the clinical efficacy of metallic stents was superior to that in patients with CBD obstruction. We believe that placement of metallic stents is the procedure of choice for palliation of malignant biliary obstruction.
本前瞻性研究的目的是评估金属支架作为无法手术的恶性胆管梗阻患者初始姑息治疗的长期临床疗效。
1991年8月至1995年5月,连续100例恶性胆管梗阻患者接受了金属支架经皮置入治疗。梗阻原因包括胆管癌(n = 50)、胰腺癌(n = 17)、胆囊癌(n = 6)、肝细胞癌(n = 2)以及肝十二指肠韧带转移性淋巴结病(n = 25)。我们使用了123枚支架:64枚Gianturco Z支架、39枚Hanaro螺旋支架、16枚Wallstent支架、2枚钽制Strecker支架、1枚Endocoil支架和1枚Memotherm镍钛合金支架。除死亡患者外,每3个月对所有患者进行随访。平均随访时间为220天(范围4 - 1125天)。通过寿命表分析评估患者生存率和支架通畅率。
整个患者组的中位生存时间为246天:25周和50周生存率分别为62%和25%。我们发现肝门部梗阻患者(256天)和胆总管(CBD)梗阻患者(227天)的中位生存时间在统计学上无显著差异。胆管癌患者的中位生存期(269天)长于其他疾病患者(197天)。所有支架的总体中位通畅时间为360天;25周和50周通畅率分别为81%和53%。在中位生存时间时支架通畅率为71%。肝门部梗阻患者的支架中位通畅时间(617天)几乎是CBD梗阻患者(324天)的两倍。然而,胆管癌患者的支架中位通畅时间与其他疾病患者的中位通畅时间在统计学上无显著差异。4例患者(4%)在支架置入后1个月内死亡。21例患者(21%)出现复发性黄疸或胆管炎。按发生频率排序,复发性黄疸的原因依次为肿瘤过度生长、胆泥结痂、肿瘤侵犯导致十二指肠梗阻、支架嵌入胆管壁、支架位置不当以及肿瘤长入。
金属支架在患者生存方面显示出良好的通畅率。在肝门部梗阻患者中,金属支架的临床疗效优于CBD梗阻患者。我们认为金属支架置入是恶性胆管梗阻姑息治疗的首选方法。