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. 2024 Mar 6;14(5):564. doi: 10.3390/diagnostics14050564

Table 4.

Studies of EUS-RFA and EUS-PDT for Unresectable PDAC.

Author, Year n Study Groups Indications Outcomes Adverse Events (AEs, %)
Song 2016 [115] 6 EUS-RFA PDAC Technical success 100% No major AEs, mild abdominal pain (33%)
Scopelliti 2018 [117] 10 EUS-RFA PDAC Technical success 100% No major AEs, mild abdominal pain (20%)
Crino 2018 [116] 8 EUS-RFA PDAC Technical success 100%, Pancreatic mass reduced 30% at 1 month No major AEs, mild abdominal pain (38%)
Jiang 2021 [118] 8 EUS-RFA PDAC Technical success 100%
Pancreatic mass reduced 34% at 1 month
No major AEs
Oh 2022 [119] 22 EUS-RFA PDAC Technical success 100%
Median survival 24 months
Peritonitis (5%), mild abdominal pain (14%)
Thosani 2022 [120] 10 EUS-RFA PDAC Technical success 100%
Tumor regression 78%
Median survival 21 months
No major AEs, abdominal pain (55%)
Kongkam 2023 [121] 22 EUS-RFA + chemotherapy (10)
Chemotherapy alone (12)
PDAC Higher rate of tumor necrosis, slower rate in tumor growth, and less narcotics in RFA group
No difference on survival
No major AEs, mild acute pancreatitis (1 patients with RFA)
Choi 2015 [127] 4 (only 1 PDAC) EUS-PDT Locally advanced pancreaticobiliary malignancies (two: Caudate lobe, one: distal bile duct, one: pancreatic tail) Disease was stable in all patients in follow up of 5 months No AEs
DeWitt 2017 [128] 12 EUS-PDT PDAC Technical success 100%, tumor necrosis in 50% of patients, tumor downstaging that permitted surgical resection in 2 patients No major AEs, 33% had sunburned hands from sun exposure, nausea, photosensitivity, and skin hyperpigmentation
Hanada 2021 [129] 8 EUS-PDT PDAC Treatment necrosis 63%
7 patients had survival duration of 209 days and one patient had survival duration of 407 days
No major AEs
Day 2: moderate abdominal pain (13%), minimal pain (53%)
Day 14: abdominal pain and diarrhea (12.5), abdominal pain requiring ER visit (12.5), hematochezia (12.5)

PDAC: pancreatic ductal adenocarcinoma; RFA: radiofrequency ablation; PDT: photodynamic therapy; G1: Group 1, G2: Group 2.