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PIPAC - Pressurized IntraPeritoneal Aerosol Chemotherapy - Cancer under Pressure (Hardcover, Digital original)
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PIPAC - Pressurized IntraPeritoneal Aerosol Chemotherapy - Cancer under Pressure (Hardcover, Digital original)
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Peritoneal dissemination is a common route of cancer metastasis.
The benefit of administering chemotherapy directly into the
peritoneal cavity is supported by preclinical and pharmacokinetic
data. In comparison to intravenous (IV) treatment, intraperitoneal
(IP) administration results in a several-fold increase in drug
concentration within the abdominal cavity. There is now growing
evidence from clinical studies showing a survival advantage for IP
chemotherapy in various tumor typies, including ovarian, gastric
and colorectal cancer. However, while the use of IP chemotherapy is
slowly gaining acceptance, it is not universal, largely due to the
greater toxicity associated with this approach. Moreover, efficacy
of IP chemotherapy is limited by poor distribution within the
abdominal cavity and by poor tissue penetration. A new way of IP
chemotherapy is the application of cytotoxics in form of a
pressurized aerosol into the abdominal of thoracic cavity.
Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is applied
through laparoscopic access using two balloon trocars in an
operating room equipped with laminar air-flow. In a first step,a
normothermic capnoperitoneum is established with a pressure of 12
mmHg. A cytotoxic solution (about 10% of a normal systemic dose) is
nebulized with a micropump into the abdominal cavity, and
maintained for 30 min. The aerosol is then removed through a closed
suction system. Applying an aerosol in the peritoneal cavity allows
a homogeneous distribution of the chemotherapeutic agent within the
abdomen. Furthermore, an artificial pressure gradient is generated
that overcomes tumoral interstitial fluid pressure, an obstacle in
cancer therapy. This results in a higher local drug concentration
compared to conventional IP or IV chemotherapy. At the same time
the plasma concentration of the chemotherapeutic agent remains low.
In first clinical studies with limited number of patients in
ovarian, gastric and colorectal cancer, as well as peritoneal
mesothelioma, PIPAC has obtained encouraging tumor response rates
and survival, with a low-side effects profile. Larger clinical
trials are currently ongoing to examine if these data can be
reproduced and extrapolated to other situations.
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