New method
Experimental endoscopy
US-guided application of a new hybrid probe in human pancreatic adenocarcinoma: an ex vivo study

https://doi.org/10.1016/j.gie.2010.02.014Get rights and content

Background

Ablative therapies such as radiofrequency and cryotechnology are widely used in oncological intervention but not in the pancreatic field because of their high operative risks. A new flexible bipolar ablation device (Cryotherm probe [CTP]) was developed combining radiofrequency and cryotechnology.

Objective

To evaluate the efficacy of the CTP in destroying neoplastic tissue of explanted pancreatic tumors of patients with pancreatic adenocarcinoma.

Design

Ex vivo clinical study.

Setting

Inpatient hospital setting.

Patients

This study involved 16 explanted pancreatic tumors from 16 patients.

Interventions

CTP application was performed on explanted pancreatic tumors. Anatomic specimens were divided into 4 groups; each group received a predefined application time of 120 to 600 seconds.

Main Outcome Measurements

The coagulation diameter (short axis) perpendicular to the device's longitudinal axis was used as the primary outcome measure.

Results

All pancreatic specimens showed histological signs of coagulative necrosis. There was a positive correlation between the short axis of the obtained necrosis and duration of application (r = 0.74).

Limitations

This study was an ex vivo study with all limitations typical of this kind of study.

Conclusions

The CTP is effective in destroying neoplastic pancreatic tissue, creating an ablation zone, the extent of which is related to the duration of application.

Section snippets

Patients and methods

Sixteen patients (8 men, age 59 ± 13 years) who underwent pancreatic resection were enrolled. The study protocol was approved by the institutional review board of Scientific Institute San Raffaele (number CTP ex vivo 2007).

Immediately after resection, pancreatic specimens were treated by CTP. Surface real-time US was used to guide the CTP into the tumor by using a 7.5- to 10-MHz probe (Fig. 3). During application, a hyperechoic area appeared around the distal tip (diameter of the active part

Results

The tumor size was 29 ± 9 mm (range 20-42 mm). All 16 pancreatic specimens were related to adenocarcinoma and showed histological signs of coagulative necrosis. The ablated area was restricted to within the tumor.

Histological analysis of the specimens showed 2 different areas: the first with defined coagulative necrosis (zone A) and the second with edema and cellular damage, but with no signs of cellular death (zone B) (Fig. 4).

The diameter of the mean short axis of the zone A, varied from 10

Discussion

RFA of pancreatic tumors bears a major risk of thermal injury to important adjacent structures such as the bile duct, the duodenum, and the larger vessels around the pancreas. The CTP is the first device to combine RF and cryotechnology and was designed to be used under EUS guidance. This new device was developed to achieve the maximum ablation size within the shortest time technically possible, which is especially important for endoscopic therapies in the clinical setting. We applied the CTP

References (8)

There are more references available in the full text version of this article.

Cited by (30)

  • Endoscopic ultrasound-guided therapies for pancreatic solid tumors: An overview

    2021, Seminars in Oncology
    Citation Excerpt :

    Importantly, systemic immunostimulating effects secondary to the activation of peritumoral immunological and systemic cell-mediated responses can also contribute to the therapeutic effect [20-22] and may be useful for specific immunotherapy combinations [23-24]. After animal and ex vivo studies [25,26], a single prospective, feasibility report on the use of the HybridTherm probe (ERBE Elektromedizin GmbH, Tübingen, Germany), a flexible bipolar RFA probe, internally carbon dioxide-cooled, with a length of 150 cm (Fig. 1), in 22 patients with unresectable stage III PDAC has been published [27]. The RFA power of 18W was delivered with a mean application time of 107 ± 86 seconds, based on tumor size.

  • Devices for endoscopic ultrasound-guided tissue acquisition

    2018, Techniques in Gastrointestinal Endoscopy
    Citation Excerpt :

    The EUS-RFA probes are available as a “through-the-needle” device (Habib EUS-RFA catheter (EMcision Ltd, London, UK)) and as an “EUS-FNA needle-type” device (19 G EUS-FNA needle electrode (Radionics Inc, Burlington, MA), 14 G hybrid cryotherm probe (Hybrid-Therm; ERBE, Tübingen, Germany), and 19 G EUSRA RF electrode (STARmed, Koyang, Korea) (Table 3). The Hybrid cryotherm probe is bipolar and the rest are monopolar probes [57]. All the RF probes are connected to generators to deliver accurate energy to the target lesion.

  • Feasibility and safety of EUS-guided cryothermal ablation in patients with locally advanced pancreatic cancer

    2012, Gastrointestinal Endoscopy
    Citation Excerpt :

    The firm position during the treatment was helpful in controlling the ablation area and avoiding sonographic artifacts. According to the previous studies6-8 and to the distance between the electrodes of the active part of the probe, a tumor size with a longitudinal axis ≥2 cm was eligible for inclusion into the study. There were no restrictions to location within the pancreas.

View all citing articles on Scopus

DISCLOSURE: The following authors disclosed financial relationships relevant to this publication: M.C. Petrone: Grant support from ERBE Elektromedizin GmbH. M.D. Enderle: Employee of ERBE Elektromedizin GmbH. A. Neugebauer: Employee of ERBE Elektromedizin GmbH. The other authors disclosed no financial relationships relevant to this publication.

If you would like to chat with an author of this article, you may contact Dr. Petrone at [email protected].

View full text