Abstract

Pressurized intraperitoneal aerosol chemotherapy (PIPAC) has emerged as a novel method to treat extensive, small volume peritoneal metastases. The clinical use of chemotherapy containing aerosols represents a potential occupational health hazard. We report the results of toxicological analysis during the first two clinical PIPAC procedures performed at Ghent University Hospital. After extensive preparation and in vitro testing, two patients were treated with PIPAC: the first using doxorubicin (2.86 mg in 51.43 mL) and cisplatin (14.28 mg in 164.3 mL), the second using oxaliplatin (182.10 mg in 186.42 mL). A standardized safety checklist was developed and used. Aerosol delivery was combined with electrostatic precipitation (ePIPAC). The following samples were obtained at several time points and locations: environmental air, floor surface wipes, surgeon's gloves, surgeon's hand wipes, circuit filters, and fluid from the water seal collection chamber container placed along the closed aerosol waste evacuating line. Platinum concentration was measured in these samples using voltammetry. Sample collection and analysis were performed by an independent external laboratory. Platinum was not detected on the four floor locations after both procedures (detection limit 0.02 ng/cm2). Similarly, no platinum was detected in environmental air during both PIPACs at the surgeon's or anesthesiologist's position (detection limit 4.0-27 ng/m3). No platinum contamination was detected on the hands, outer pair of gloves, or inner pair of gloves of the surgeon (detection limit 70 and 50 ng respectively). Platinum was not detected on the filters and in the air-seal container liquid. With adequate preparation and precautions, a clinical PIPAC program can be established without measurable chemotherapy exposure to the operating room environment or healthcare workers.

Highlights

  • Peritoneal metastasis is a defining feature of stage III ovarian cancer and occurs in approximately 13 % of gastric cancers, 9 % of pancreas cancers, and 8 % of colorectal cancers [1,2,3,4]

  • *Corresponding author: Wim Ceelen, Department of GI Surgery, Ghent University Hospital, route 1275, De Pintelaan 185, 9000, Ghent, Belgium; Cancer research institute Ghent (CRIG), Ghent, Belgium, E-mail: Wim.ceelen@ugent.be Wouter Willaert, Department of GI Surgery, Ghent University Hospital, route 1275, De Pintelaan 185, 9000, Ghent, Belgium, E-mail: wouter.willaert@ugent.be Paul Sessink, Exposure Control Sweden AB, Bohus-Björkö, Sweden, E-mail: info@exposurecontrol.nl not detected on the filters and in the air-seal container liquid

  • With adequate preparation and precautions, a clinical PIPAC program can be established without measurable chemotherapy exposure to the operating room environment or healthcare workers

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Summary

Introduction

Peritoneal metastasis is a defining feature of stage III ovarian cancer and occurs in approximately 13 % of gastric cancers, 9 % of pancreas cancers, and 8 % of colorectal cancers [1,2,3,4]. The aerosol is generated by a high pressure line connected to a nozzle, the term pressurized intraperitoneal aerosol chemotherapy or PIPAC. Advantages of this approach include minimal morbidity, efficient drug distribution, and tissue penetration, and the possibility to repeat the procedure which allows for visual and histological assessment of treatment response. Small volume but unresectable peritoneal metastasis, preliminary clinical experience has demonstrated the safety and antitumor efficacy of PIPAC [9,10,11]. Pressurized intraperitoneal aerosol chemotherapy (PIPAC) has emerged as a novel method to treat extensive, small volume peritoneal metastases. Results: Platinum was not detected on the four floor locations after both procedures (detection limit 0.02 ng/ cm).

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