A Phase I Dose Escalation Study of Oxaliplatin, Cisplatin and Doxorubicin Applied as PIPAC in Patients with Peritoneal Carcinomatosis
Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) is an innovative laparoscopic intraperitoneal chemotherapy approach with the advantage of a deeper tissue penetration. Thus far, oxaliplatin has been administered at an arbitrary dose of 92 mg/m<sup>2</sup>, cisplatin at 7.5 mg/m&l...
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doaj-4b2b28ee678b48428920aacc9cc7a0172021-03-04T00:00:37ZengMDPI AGCancers2072-66942021-03-01131060106010.3390/cancers13051060A Phase I Dose Escalation Study of Oxaliplatin, Cisplatin and Doxorubicin Applied as PIPAC in Patients with Peritoneal CarcinomatosisManuela Robella0Michele De Simone1Paola Berchialla2Monica Argenziano3Alice Borsano4Shoeb Ansari5Ornella Abollino6Eleonora Ficiarà7Armando Cinquegrana8Roberta Cavalli9Marco Vaira10Unit of Surgical Oncology, Candiolo Cancer Institute, FPO—IRCCS, 10060 Candiolo, ItalyUnit of Surgical Oncology, Candiolo Cancer Institute, FPO—IRCCS, 10060 Candiolo, ItalyDepartment of Clinical and Biological Sciences, University of Torino, 10126 Torino, ItalyDepartment of Drug Science and Technology, University of Torino, 10125 Torino, ItalyUnit of Surgical Oncology, Candiolo Cancer Institute, FPO—IRCCS, 10060 Candiolo, ItalyDepartment of Drug Science and Technology, University of Torino, 10125 Torino, ItalyDepartment of Drug Science and Technology, University of Torino, 10125 Torino, ItalyDepartment of Neuroscience, University of Torino, 10126 Torino, ItalyUnit of Surgical Oncology, Candiolo Cancer Institute, FPO—IRCCS, 10060 Candiolo, ItalyDepartment of Drug Science and Technology, University of Torino, 10125 Torino, ItalyUnit of Surgical Oncology, Candiolo Cancer Institute, FPO—IRCCS, 10060 Candiolo, ItalyPressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) is an innovative laparoscopic intraperitoneal chemotherapy approach with the advantage of a deeper tissue penetration. Thus far, oxaliplatin has been administered at an arbitrary dose of 92 mg/m<sup>2</sup>, cisplatin at 7.5 mg/m<sup>2</sup> and doxorubicin 1.5 mg/m<sup>2</sup>. This is a model-based approach phase I dose escalation study with the aim of identifying the maximum tolerable dose of the three different drugs. The starting dose of oxaliplatin was 100 mg/m<sup>2</sup>; cisplatin was used in association with doxorubicin: 15 mg/m<sup>2</sup> and 3 mg/m<sup>2</sup> were the respective starting doses. Safety was assessed according to Common Terminology Criteria for Adverse Events (CTCAE version 4.03). Thirteen patients were submitted to one PIPAC procedure. Seven patients were treated with cisplatin and doxorubicin and 6 patients with oxaliplatin; no dose limiting toxicities and major side effects were found. Common adverse events included postoperative abdominal pain and nausea. The maximum tolerable dose was not reached. The highest dose treated cohort (oxaliplatin 135 mg/m<sup>2</sup>; cisplatin 30 mg/m<sup>2</sup> and doxorubicin 6 mg/m<sup>2</sup>) tolerated PIPAC well. Serological analyses revealed no trace of doxorubicin at any dose level. Serum levels of cis- and oxaliplatin reached a peak at 60–120 min after PIPAC and were still measurable in the circulation 24 h after the procedure. Cisplatin and doxorubicin may be safely used as PIPAC at a dose of 30 mg/m<sup>2</sup> and 6 mg/m<sup>2</sup>, respectively; oxaliplatin can be used at an intraperitoneal dose of 135 mg/m<sup>2</sup>. The dosages achieved to date are the highest ever used in PIPAC.https://www.mdpi.com/2072-6694/13/5/1060PIPACperitoneal carcinomatosischemotherapyphase Ilocoregional |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Manuela Robella Michele De Simone Paola Berchialla Monica Argenziano Alice Borsano Shoeb Ansari Ornella Abollino Eleonora Ficiarà Armando Cinquegrana Roberta Cavalli Marco Vaira |
spellingShingle |
Manuela Robella Michele De Simone Paola Berchialla Monica Argenziano Alice Borsano Shoeb Ansari Ornella Abollino Eleonora Ficiarà Armando Cinquegrana Roberta Cavalli Marco Vaira A Phase I Dose Escalation Study of Oxaliplatin, Cisplatin and Doxorubicin Applied as PIPAC in Patients with Peritoneal Carcinomatosis Cancers PIPAC peritoneal carcinomatosis chemotherapy phase I locoregional |
author_facet |
Manuela Robella Michele De Simone Paola Berchialla Monica Argenziano Alice Borsano Shoeb Ansari Ornella Abollino Eleonora Ficiarà Armando Cinquegrana Roberta Cavalli Marco Vaira |
author_sort |
Manuela Robella |
title |
A Phase I Dose Escalation Study of Oxaliplatin, Cisplatin and Doxorubicin Applied as PIPAC in Patients with Peritoneal Carcinomatosis |
title_short |
A Phase I Dose Escalation Study of Oxaliplatin, Cisplatin and Doxorubicin Applied as PIPAC in Patients with Peritoneal Carcinomatosis |
title_full |
A Phase I Dose Escalation Study of Oxaliplatin, Cisplatin and Doxorubicin Applied as PIPAC in Patients with Peritoneal Carcinomatosis |
title_fullStr |
A Phase I Dose Escalation Study of Oxaliplatin, Cisplatin and Doxorubicin Applied as PIPAC in Patients with Peritoneal Carcinomatosis |
title_full_unstemmed |
A Phase I Dose Escalation Study of Oxaliplatin, Cisplatin and Doxorubicin Applied as PIPAC in Patients with Peritoneal Carcinomatosis |
title_sort |
phase i dose escalation study of oxaliplatin, cisplatin and doxorubicin applied as pipac in patients with peritoneal carcinomatosis |
publisher |
MDPI AG |
series |
Cancers |
issn |
2072-6694 |
publishDate |
2021-03-01 |
description |
Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) is an innovative laparoscopic intraperitoneal chemotherapy approach with the advantage of a deeper tissue penetration. Thus far, oxaliplatin has been administered at an arbitrary dose of 92 mg/m<sup>2</sup>, cisplatin at 7.5 mg/m<sup>2</sup> and doxorubicin 1.5 mg/m<sup>2</sup>. This is a model-based approach phase I dose escalation study with the aim of identifying the maximum tolerable dose of the three different drugs. The starting dose of oxaliplatin was 100 mg/m<sup>2</sup>; cisplatin was used in association with doxorubicin: 15 mg/m<sup>2</sup> and 3 mg/m<sup>2</sup> were the respective starting doses. Safety was assessed according to Common Terminology Criteria for Adverse Events (CTCAE version 4.03). Thirteen patients were submitted to one PIPAC procedure. Seven patients were treated with cisplatin and doxorubicin and 6 patients with oxaliplatin; no dose limiting toxicities and major side effects were found. Common adverse events included postoperative abdominal pain and nausea. The maximum tolerable dose was not reached. The highest dose treated cohort (oxaliplatin 135 mg/m<sup>2</sup>; cisplatin 30 mg/m<sup>2</sup> and doxorubicin 6 mg/m<sup>2</sup>) tolerated PIPAC well. Serological analyses revealed no trace of doxorubicin at any dose level. Serum levels of cis- and oxaliplatin reached a peak at 60–120 min after PIPAC and were still measurable in the circulation 24 h after the procedure. Cisplatin and doxorubicin may be safely used as PIPAC at a dose of 30 mg/m<sup>2</sup> and 6 mg/m<sup>2</sup>, respectively; oxaliplatin can be used at an intraperitoneal dose of 135 mg/m<sup>2</sup>. The dosages achieved to date are the highest ever used in PIPAC. |
topic |
PIPAC peritoneal carcinomatosis chemotherapy phase I locoregional |
url |
https://www.mdpi.com/2072-6694/13/5/1060 |
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