Experimental animals and study protocol
This study was conducted at the National Cancer Center Hospital East, Kashiwa, Japan. The study protocol was approved by the Animal Experiment Committee in National Cancer Center JapanK18-024, 2018/12/27), and all animal experiments were conducted in accordance with the Institutional guidelines and the ARRIVE guidelines (http://www.nc3rs.org.uk/page.asp?id=1357). We included three female pigs (weight 40–45 kg). The study protocol was designed to minimize pain or discomfort to the animals. To evaluate the feasibility of combination therapy in the various situation, we created four lesions on each of the three porcine normal esophagi using a DualKnife™ (Olympus, Tokyo, Japan). We employed three combination therapy strategies: (a) simultaneous procedure of EMR and CbFAS for Pig A, (b) CbFAS for post-EMR scar for Pig B, and (c) ER for post-CbFAS scar for Pig C. All EMR procedures were performed through EMR using the Cap method (EMR).
Study procedures
In vivo porcine specimens were obtained under general anesthesia: sedation was induced with intramuscular midazolam (1 mg/kg) and ketamine (15 mg/kg), and anesthesia was induced and maintained with propofol (3 mg/kg initially, and 6 mg/kg/h, respectively). The details of procedural protocol in each pig were as follows. In Pig A, we simultaneously used EMR and CbFAS (ER + CbFAS; the CbFAS was done immediately after EMR for a post-EMR mucosal defect), wherein EMR + CbFAS were undertaken at two lesions on Day 1, and at another two lesions on Day 28 (Fig. 1) (Supplementary Video). In Pig B, we conducted CbFAS for a post-EMR scar; the EMR was done for two lesions on Day 1, and the CbFAS was carried out on two lesions of EMR scarring as well as at two lesions with normal mucosa on Day 28 after the EMR (Fig. 2). In Pig C, we conducted EMR for post-CbFAS scarring; CbFAS was done for two lesions on Day 1, and EMR was carried out for two lesions on the post-CbFAS scarring as well as for two normal lesions on Day 28. All endoscopic procedures were undertaken as scheduled by three surgeons. (HS, YY. TY)
Cryoablation
We used the CryoBalloon focal ablation system (CbFAS; C2 Cryoballoon, HOYA Pentax Medical, Japan) in this study. The CbFAS comprises a portable hand-held Controller, a catheter with a self-sizing balloon with a spray hole located on a diffuser, foot pedal for adjusting the balloon and the diffuser, and a single-use cartridge of liquid nitrous oxide. The distal tip of the catheter (diameter 3.6 mm) is advanced through a PENTAX EG34-i10 therapeutic endoscope channel (HOYA Pentax Medical, Japan) and the proximal end is connected to the Controller to operate the catheter with the foot pedal. From the cartridge, which is also connected to the Controller, liquid nitrous oxide (−85°C) is released through the catheter. By rotating the diffuser clockwise or counterclockwise, the spray hole can be directed to the targeted area. The balloon probe is placed in contact with the tissue wall of the target region, and cryogenic fluid is sprayed while visualizing the target site through the balloon. A single application created an ice patch of approximately 2 cm2 on the targeted mucosa. Ablations of 8 seconds durations were performed in this study.
Endoscopic mucosal resection using a cap-fitted endoscope
The EMR technique requires a specialized transparent cap that is fitted to the tip of an endoscope. Saline is injected into the submucosa. The crescent-shaped snare (Olympus, Tokyo, Japan) is then pre-looped into the groove of the rim of the cap. Then, the lesion is suctioned with medium to high vacuum into the cap. After the endoscopist strangulates the lesion by closing the snare, electrosurgical current is used to resect the lesion.
Outcomes
The primary outcome was to evaluate the feasibility of combination treatment. We evaluated the technical success (defined treatment completion as intended) and device malfunction (defined as any failure in CbFAS components requiring device replacement). In addition, the difficulty of each process in all procedures, including injection of saline into the submucosa, lifting the mucosa, and snaring and cutting in ER, and stabilizing the balloon and ablation in CbFAS, was recorded. The degree of difficulty was classified into three levels: easy, moderate, and difficult. Easy was defined by the procedure being performed without any problems, and difficult as instances when the procedure had failed several times and needed to be repeated, or when the treatment was not performed as planned. Moderate was defined as being intermediate in terms of ease and difficulty. In addition, all procedures were evaluated as easy or moderate in the technical success case. The secondary outcome was safety. We evaluated bleeding and perforation during treatment and esophageal stenosis, weight loss/gain, and anorexia during this study period.
Histopathological analysis
All animals were euthanized by intravenous injection of potassium chloride on days 32 after the initial procedure, and tissue specimens of EMR were harvested for histopathological examination. Histopathological outcomes were evaluated on the basis of tissue damage on days 5 and 32 after treatment. Tissue sections were prepared from samples of the ablated areas and EMR specimens. All specimens were fixed in formalin (10%), embedded in paraffin, and stained with hematoxylin and eosin. Slices of the specimens were evaluated for depth of tissue damage and tissue finding caused by ablation damage in the esophageal wall. All specimens were assessed by a gastrointestinal pathologist.