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Endoscopic ultrasound-guided radiofrequency ablation (EUS-RFA) for advanced pancreatic and periampullary adenocarcinoma
被引:32
|作者:
Thosani, Nirav
[1
]
Cen, Putao
[2
]
Rowe, Julie
[2
]
Guha, Sushovan
[1
]
Bailey-Lundberg, Jennifer M.
[3
]
Bhakta, Dimpal
[1
]
Patil, Prithvi
[1
]
Wray, Curtis J.
[4
]
机构:
[1] Univ Texas Hlth Sci Ctr Houston, Dept Med, Ctr Intervent Gastroenterol, Houston, TX 77030 USA
[2] Univ Texas Hlth Sci Ctr Houston, Dept Med, Div Oncol, McGovern Med Sch, Houston, TX 77030 USA
[3] Univ Texas Hlth Sci Ctr Houston, Dept Anesthesia, Houston, TX 77030 USA
[4] Univ Texas Hlth Sci Ctr Houston, Dept Surg, 6431 Fannin St,MSB 4-164a, Houston, TX 77030 USA
关键词:
CANCER;
SURVIVAL;
CHEMOTHERAPY;
PANCREATICODUODENECTOMY;
GEMCITABINE;
RESECTION;
IMPROVES;
THERAPY;
D O I:
10.1038/s41598-022-20316-2
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Long term prognosis and 5-year survival for pancreatic adenocarcinoma (PDAC) remains suboptimal. Endoscopic ultrasound (EUS) guided RFA (EUS-RFA) is an emerging technology and limited data exist regarding safety and long-term outcomes. The aim of this study is to report safety-profile, feasibility and outcomes of EUS-RFA for advanced PDAC. Prospective review of patients with diagnosis of locally-advanced or metastatic PDAC undergoing EUS-RFA between October 2016 to March 2018 with long-term follow up (> 30 months). Study patients underwent a total of 1-4 RFA sessions. All patients were enrolled in longitudinal cohort study and received standard of care chemotherapy. 10 patients underwent EUS-RFA. Location of the lesions was in the head(4), neck(2), body(2), and tail(2). 22 RFA sessions were performed with a range of 1-4 sessions per patient. There were no major adverse events (bleeding, perforation, infection, pancreatitis) in immediate (up to 72 h) and short-term follow up (4 weeks). Mild worsening of existing abdominal pain was noted during post-procedure observation in 12/22 (55%) of RFA treatments. Follow-up imaging demonstrated tumor progression in 2 patients, whereas tumor regression was noted in 6 patients (> 50% reduction in size in 3 patients). Median survival for the cohort was 20.5 months (95% CI, 9.93-42.2 months). Currently, 2 patients remain alive at 61 and 81 months follow-up since initial diagnosis. One patient had 3 cm PDAC with encasement of the portal confluence, abutment of the celiac axis, common hepatic and superior mesenteric artery. This patient had significant reduction in tumor size and underwent standard pancreaticoduodenectomy. In our experience, EUS-RFA was safe, well-tolerated and could be concurrently performed with standard chemotherapy. In this select cohort, median survival was improved when compared to published survival based upon SEER database and clinical trials. Future prospective trials are needed to understand the role of EUS-RFA in overall management of PDAC.
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