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新辅助治疗胰腺癌患者中自膨式金属支架胆道减压的疗效和安全性:一项前瞻性研究。

Efficacy and safety of self-expandable metal stents for biliary decompression in patients receiving neoadjuvant therapy for pancreatic cancer: a prospective study.

机构信息

Division of Gastroenterology and Hepatology, Medical College of Wisconsin and Veterans Affairs Medical Center, Milwaukee, Wisconsin 53226, USA.

出版信息

Gastrointest Endosc. 2012 Jul;76(1):67-75. doi: 10.1016/j.gie.2012.02.041. Epub 2012 Apr 5.

Abstract

BACKGROUND

Increasing numbers of patients with resectable pancreatic cancer are receiving neoadjuvant therapy. Biliary drainage with plastic stents during this period can be associated with recurrent episodes of stent occlusion resulting in unplanned ERCPs and interruptions in therapy.

OBJECTIVE

To evaluate the efficacy and safety of self-expandable metal stents (SEMSs) during the neoadjuvant period for resectable pancreatic cancer.

DESIGN

Patients with proven pancreatic adenocarcinoma with biliary obstruction underwent placement of SEMSs, and data on stent patency and complication rates were collected prospectively.

SETTING

Tertiary-care referral center.

PATIENTS

This study involved 55 patients with resectable and borderline resectable pancreatic duct adenocarcinoma who were recruited between March 2009 and December 2010.

INTERVENTION

SEMSs were placed for biliary decompression. The shortest length of stent required to bridge the stricture was used so as to leave enough of the normal bile duct above the stent available for subsequent surgical anastomosis. Endoscopic reintervention was performed in those with stent malfunction. Stents were not removed before surgery.

MAIN OUTCOME MEASUREMENTS

Stent patency rate during the neoadjuvant period, stent malfunction rate, and complication rates. Information on stent-related difficulties, if any, during surgery.

RESULTS

Fifty-five patients were recruited (29 men, 26 women; age, mean [± SD] 65.9 ± 11 years; resectable 23, borderline resectable 32). Median time for neoadjuvant therapy and restaging before surgery was 104 days (range 70-260 days). At the median time of 104 days, 88% of SEMSs remained patent. By 260 days, stent malfunction occurred in 15% of patients. These included stent occlusion in 13% and stent migration in 2%. SEMS malfunction occurred in 3 of 27 patients (11%) who ultimately underwent pancreaticoduodenectomy and in 5 of 21 patients (24%) with disease progression (P = not significant). The presence of SEMSs did not interfere with pancreaticoduodenectomy in any patients who underwent surgery.

LIMITATIONS

Nonrandomized study.

CONCLUSION

SEMSs are effective and safe in achieving durable biliary drainage in patients with pancreatic cancer receiving neoadjuvant therapy. It is not necessary to remove SEMSs before surgery if the shortest length of stent required to bridge the stricture is used.

摘要

背景

越来越多的可切除胰腺癌患者接受新辅助治疗。在此期间,使用塑料支架进行胆道引流可能会导致支架再次阻塞,导致计划外的内镜逆行胰胆管造影术 (ERCP) 和治疗中断。

目的

评估可切除胰腺癌新辅助治疗期间使用自膨式金属支架 (SEMS) 的疗效和安全性。

设计

经证实患有胰腺腺癌伴胆道梗阻的患者接受 SEMS 置入,并前瞻性收集支架通畅率和并发症发生率数据。

地点

三级转诊中心。

患者

这项研究涉及 55 名可切除和边缘可切除的胰腺导管腺癌患者,他们于 2009 年 3 月至 2010 年 12 月期间被招募。

干预措施

SEMS 用于胆道减压。使用最短长度的支架来桥接狭窄部位,以便在支架上方留有足够的正常胆管,以便进行后续的手术吻合。支架功能障碍者进行内镜再介入治疗。在手术前不取出支架。

主要观察指标

新辅助治疗期间的支架通畅率、支架功能障碍率和并发症发生率。如果有任何与支架相关的困难,在手术期间的信息。

结果

共招募 55 名患者(29 名男性,26 名女性;年龄,平均[±标准差]65.9±11 岁;可切除 23 例,边缘可切除 32 例)。新辅助治疗和手术前重新分期的中位时间为 104 天(范围 70-260 天)。在中位时间 104 天时,88%的 SEMS 仍保持通畅。到 260 天时,支架功能障碍的发生率为 15%。其中支架阻塞占 13%,支架迁移占 2%。3 例(11%)最终接受胰十二指肠切除术和 5 例(24%)疾病进展的患者(P = 无显著差异)发生支架功能障碍。支架的存在并没有干扰任何接受手术的患者的胰十二指肠切除术。

局限性

非随机研究。

结论

SEMS 可有效、安全地实现接受新辅助治疗的胰腺癌患者持久的胆道引流。如果使用最短长度的支架来桥接狭窄部位,则无需在手术前取出 SEMS。

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