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. 2021 Mar;10(3):1271-1275.
doi: 10.21037/gs-2019-ursoc-11.

Rotational intraperitoneal pressurized aerosol chemotherapy in a porcine model

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Rotational intraperitoneal pressurized aerosol chemotherapy in a porcine model

Jaehee Mun et al. Gland Surg. 2021 Mar.

Abstract

Peritoneal carcinomatosis (PC) commonly represent drug resistance to intravenous (IV) chemotherapy in advanced or recurrent disease of solid tumors. For improving the prognosis of PC, intraperitoneal (IP) chemotherapy has been introduced in the clinical setting, and phase III trials proved the superiority of IP chemotherapy to IV chemotherapy, in particular, in advanced ovarian cancer. However, increased toxicities by IP chemotherapy lead to reduced cycles of chemotherapy, which does not guarantee its effectiveness. Moreover, hyperthermic IP chemotherapy after cytoreductive surgery also showed improved survival compared to IV chemotherapy in advanced ovarian cancer. Nevertheless, limited distribution and diffusion of drugs, and grade 3 or 4 renal and hepatic toxicity of 20% preclude the expansion of its application. On the other hand, pressurized intraperitoneal aerosol chemotherapy (PIPAC) is known to show the effect by delivering drugs to the parietal and visceral peritoneum in the form of aerosol under the abdominal pressure of 12 mmHg induced by laparoscopic system. Although low dose equivalent to about 1% dose of resistant drugs for IV chemotherapy and normothermia are used in PIPAC, it may improve tumor response and quality of life by repetitive application of PIPAC due to the increased distribution and penetration depth of drugs. However, the heterogeneous distribution of drugs is still the major limitation of PIPAC because the nozzle is placed at the possible outlying position to the tumor-bearing tissues during laparoscopic surgery. Therefore, we developed a novel prototype for PIPAC, rotational intraperitoneal pressurized aerosol chemotherapy (RIPAC) system because rotation of the nozzle and change of spray direction can contribute to homogenous distribution of drugs, and compared the distribution of drugs between PIPAC and RIPAC in a porcine model mimicking human body. As a result, RIPAC was more effective than PIPAC in terms of the distribution of drugs into the visceral and parietal peritoneum.

Keywords: Rotational; aerosol; chemotherapy; intraperitoneal (IP); pressurized.

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Conflict of interest statement

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/gs-2019-ursoc-11). The series “Ultra-Radical Surgery in Ovarian Cancer: Surgical Techniques for Gynecologic Oncologist” was commissioned by the editorial office without any funding or sponsorship. The authors have no other conflicts of interest to declare.

Figures

Video 1
Video 1
Intraperitoneal chemotherapy using pressurized intraperitoneal aerosol chemotherapy and novel prototype for pressurized intraperitoneal aerosol chemotherapy in a porcine model.
Figure 1
Figure 1
Novel prototype for PIPAC. PIPAC, pressurized intraperitoneal aerosol chemotherapy.
Figure 2
Figure 2
Setting of RIPAC in swine. RIPAC, rotational intraperitoneal pressurized aerosol chemotherapy.
Figure 3
Figure 3
Comparison of the distribution of drugs by using 1% methylene blue staining between (A) PIPAC and (B) RIPAC. PIPAC, pressurized intraperitoneal aerosol chemotherapy; RIPAC, rotational intraperitoneal pressurized aerosol chemotherapy.

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