CC BY-NC-ND 3.0 · Journal of Digestive Endoscopy 2017; 08(04): 206-209
DOI: 10.4103/jde.JDE_72_17
News and Views
Journal of Digestive Endoscopy

Endoscopic Ultrasound-Guided Pancreatic Cyst Ablation

Ravi Sharma
Department of Gastroenterology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
Surinder Singh Rana
Department of Gastroenterology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
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25. September 2019 (online)


In the recent years, due to advancement and widespread availability of imaging modalities, the incidence of pancreatic cystic lesions (PCL) has increased considerably.[1] This increased detection of asymptomatic but potentially malignant or malignant cystic lesion poses a difficult management dilemma. Pancreatic cysts can be classified into two groups as follows: (i) acute or chronic pancreatitis (acute fluid collections and pseudocysts without lining epithelium lining and no malignant potential) and (ii) cystic neoplasms lined by epithelium. The current diagnostic algorithm involves an accurate diagnosis of cystic epithelial lesions and thereafter accurate identification of malignant potential. The symptomatic cystic lesions or cysts with a malignant potential are offered surgical resection. However, surgical resection is associated with high morbidity (20%–40%) as well as mortality (~2%).[2] [3] [4] Therefore, there have been concerted efforts to develop minimally invasive treatment modalities for treatment of these patients. Endoscopic ultrasound (EUS)-guided pancreatic cyst ablation (PCA) with ethanol and/or paclitaxel has been evaluated as a minimally invasive alternative to surgery in patients who are high-risk for or refuse surgery.[5],[6] The initial results have been encouraging with complete (<5% of original cyst volume) or partial (5%–25% of original cyst volume) image-defined response documented in 60%–70% of patients and moreover, elimination of baseline cyst fluid DNA mutations has also been reported.[6],[7] However, the effect of PCA on cyst sonographic morphology, cyst fluid cytology, and the quality and quantity of cyst fluid DNA is not available, and moreover, the long-term sustainability of the ablative effect of PCA is not known. In the news and views of this issue, we discuss two studies that have looked at these lacunae in the literature.

First, a prospective single center study from Indiana University Health Hospital evaluated the morphological as well as cytological changes along with a change in cyst fluid DNA after PCA on PCL that measured 10–50 mm in diameter and contained 5 or fewer septations.[8] Majority of patients included in this needed surgical resection but surgery was refused either by patients or patient was declared unfit for surgery. Before, PCA EUS morphology (i.e. septations, cyst wall thickness, the presence of nodules) and maximal 2-dimension cross-sectional diameter was recorded. Thereafter, EUS-guided fluid aspiration was done, and quantity, viscosity, and color of fluid were recorded. The aspirated sample was also sent for cytology in all patients and carcinoembryonic antigen and molecular analysis (RedPath Integrated Technologies) in selected patients.

The protocol for PCA was variable depending on the year of enrolment as the patients were enrolled in different studies during various time periods. From 2004–2009, they underwent initial ablation with saline solution or ethanol alone (as part of a randomized trial) and from 2009 to 2014 they underwent PCA with ethanol plus paclitaxel (in a prospective cohort study). Thereafter, all patients underwent follow-up EUS 2–3 months later and during the years 2004–2009, diagnostic EUS was followed by fine-needle aspiration (FNA) for cytology and finally an index or second ethanol lavage (depending on initial randomization). Patients enrolled from 2009 to 2014 underwent follow-up diagnostic EUS, repeat EUS-FNA for cytology in all patients and molecular analysis (when possible) and finally repeat cyst ablation in patients with an initial suboptimal response. In all patients (regardless of initial ablation regimen), repeat computed tomography (CT), MRI, or EUS was performed 3–6 months later and then yearly.

The cyst volume was evaluated by two-dimensional (linear EUS) or three-dimensional (CT or MRI) measurements. Two-dimensional cyst volume was measured using formula 4/3 πr3, where r represents the radius of the maximal cyst by linear EUS image. Three-dimensional volume was calculated by the simplified formula d1 × d2 × d3/2, where d1, d2, and d3 represent the maximal diameters in the axial, coronal, and sagittal planes, respectively. The response was labeled as complete response (CR), partial response (PR), or persistent with <5%, 5% to 25%, and >25% change of the original cyst volume, respectively. Molecular analysis was performed by clinically blinded laboratory personnel. DNA was isolated by using 200 μl of pancreatic cyst fluid (Qiagen, Valencia, Calif, USA) and quantity measured by using spectrophotometer (NanoDrop, Willmington, Del, USA). DNA amplification was done by using polymerase chain reaction (PCR; i Cycler; BioRad, Hercules, Calif, USA).

The authors studied 36 patients (24 females) with a mean age of 69.1 ± 12.2 years. In 22 (61.1%) patients, the cysts were located in the body and tail with the cyst size ranging from 10 to 50 mm. The presumed clinical diagnosis was 16 (44.4%) mucinous cystic neoplasms (MCN), 14 (38.9%) branched intraductal papillary mucinous neoplasms (IPMN), 5 (13.9%) SCA and 1 pseudocyst. EUS guided PCA was initially performed by using ethanol only in eight patients and in 28 patients by using a combination of ethanol and paclitaxel injection. Second PCA was performed in 17 patients, and third PCA was performed in only one patient. Repeat PCA was not performed in 18 patients due to decrease cyst size in 11, acute pancreatitis in 3, decreased cyst size with increased internal debris (n=1), pseudocyst formation at gastric wall (n=1), markedly increased internal debris (n=1), and refusal (n=1) after the first ablation. CR, PR and nonresponse were achieved in 19 out of 34 (56%), 7 (21%), and 8 (23%) patients, respectively. A total of 54 PCA (First PCA in 36 patients + Second PCA in 17+ third PCA 1 patients) were performed, and 9 patients had procedure-related complication including pain abdomen in 4 patients. pancreatitis in 4 patients and hemorrhage in cyst in one patient.

Post-PCA, EUS was performed in 34 patients, and it showed an increase of cyst wall diameter in 23 of 34 patients, decrease in a number of cysts in 3 patients, loss of septations in 5 patients, increase in septations in 2 patients and loss of mural nodule in 5 patients. Intra-cystic debris developed in 8 patients and 1 patient developed a new mural calcification, whereas one patient developed both mural nodule loss and development of calcification. Post-PCA cytology assessed in 34 patients showed increased in epithelial cellularity in 9 patients, decrease or loss of an atypical cell in five patients and increase or newly developed atypical cell in 3 patients. Microscopically, post-PCA increase in cyst debris was observed in 12 patients, and fluid viscosity alteration was observed in 14 patients. No difference in sonographic or cytological changes was present between complete responders compared to those with a partial or nonresponse.

Preablation DNA quantity was evaluated in 20 patients who underwent PCA by using ethanol and paclitaxel, and it revealed mean DNA quantity and quality of 60.4 ± 239.6 ng/uL (range 1.6–1,078.0) and 29.3 ± 2.8 (range 24.3–36.8) (Ct value), respectively. Post-PCA DNA quantity and quality was evaluated in 17 of these 20 patients and mean postablation DNA quantity and quality were 35.8 ± 60.6 ng/uL (range 1.5–255.4) and 27.1 ± 2.9 (range 23.8–32.9), respectively. When classified by imaging response, postablation DNA amount increased in 12 out of 17 (70.6%), including 10 of 12 (83.3%) in the CR group, whereas overall, postablation DNA Ct value decreased in 12 of 17 (70.6%) patients, including 9 of 12 (75%) in CR group. For CR group, mean DNA quantity significantly increased after ablation (44.8 ± 70.7 vs. 6.7 ± 9.5, P=0.023), but there was no change in quality (P=0.136). The authors concluded that EUS-guided PCA induces morphological and cytological changes in the pancreatic cystic neoplasms, but none of these predicts overall imaging-defined response to ablation.

The second prospective study from a Korean center evaluated the long-term impact of EUS guided PCA in a large group of patients with PCL studied over 10 years period.[9] They enrolled 164 patients with PCL who underwent EUS-guided cyst ablation by using Ethanol and paclitaxel. In this study, following patients were included as follows: (i) unilocular or oligolocular cyst with 2–6 septations (ii) clinically indeterminate cyst for which EUS FNA was indicated to obtain additional information and (iii) cysts that increased in size during follow-up. All patients were asymptomatic, without abdominal pain that could be ascribed to pancreatic cysts and median largest diameter was 32 mm (interquartile range [IQR] 26–41). Sixteen patients (40.2%) had unilocular cysts and 98 patients (59.8%) had oligolocular cysts.

The cytological analysis of cyst fluid was performed in 125 (76.2%) of 164 samples and results were as follows: “negative” in 58 (46.4%), “nondiagnostic” in 52 (41.6%), “atypical cells” in 3 (2.4%), and “mucinous epithelium” in 12 (9.6%) patients. Based on the cyst fluid analysis and imaging the presumed diagnoses were as follows: MCN (n=71, 43.3%), SCN (n=16, 9.8%), IPMN (n=11, 6.7%), pseudocyst (n=3, 1.8%), and indeterminate cysts (n=63, 38.4%) patients, respectively. PCA was done using 22G needle and thereafter patients were followed up by a CT at 3 months and further follow-up CT at 6 months interval till resolution and yearly thereafter. Treatment response was assessed by comparing cyst volume at the time of PCA. Responses were arbitrarily classified as complete radiological resolution, partial resolution, or persistent cyst, corresponding to <5%, 5%–25%, and >25% of baseline cyst volume.

As six patients were lost to follow-up, 158 patients were finally analyzed with median follow-up of 69 months (IQR 48–81). Complete resolution was observed in 114 patients (72.2%) and partial resolution in 31 patients (19.6%), respectively, whereas 13 patients (8.2%) had persistent cysts. The median volume of cysts changed from 17.1 mL (IQR 13.1–25.3) at baseline to 3.1 mL (IQR 1.3–5.5) at the end of follow-up. On univariate analysis, EUS diameter (<35 mm; P=0.04) and locularity (unilocular lesion; P < 0.001) were significantly associated with complete resolution. The rates of complete resolution based on cystic fluid analysis were as follows: SCN, 87.5%; MCN, 76.1%; indeterminate cysts, 67.7%; IPMN, 50.0% (P > 0.05). On multivariate analysis, unilocular lesion (odds ratio [OR] 7.12, 95% confidence interval [CI] 2.72–18.67; P < 0.001) and smaller cyst diameter (OR 2.39, 95%CI 1.11–5.16, P=0.02) were independent predictors of complete resolution. There were 16 adverse events (9.8%; 1 severe, 4 moderate. and 11 mild) with early adverse events being fever without documented bacteremia on blood culture (n=1), pericystic spillage (n=1), intracystic hemorrhage (n=1), and acute pancreatitis (n=6) and late adverse events (after 14 days) being pseudocyst (n=2), abscess formation (n=2), portal vein thrombosis (n=1), splenic vein obliteration (n=1), and main pancreatic duct stricture requiring endoscopic stent placement (n=1).

On a follow-up of the median of 72 months, patients with initial complete resolution, radiological recurrence of the cyst was found in only two patients (1.7%) and recurrent cysts (presumed MCN 1 and indeterminate cyst 1) were found after cyst-free intervals of 36 and 48 months, respectively. More importantly, no malignancy was discovered during follow-up. The authors concluded that among patients with pancreatic cysts in whom complete resolution was achieved after EUS-guided PCA, 98.3% remained in remission at 6-year follow-up and unilocular form, as well as small cyst size, were predictive of complete resolution.