Phase I study of intraperitoneal aerosolized nanoparticle albumin based paclitaxel (NAB-PTX) for unresectable peritoneal metastases
Background Pressurized intraperitoneal aerosolized chemotherapy (PIPAC) is a novel method to treat patients with peritoneal metastases (PM). We aimed to study the tolerability, safety, pharmacokinetics, and tumour response of nanoparticle albumin bound paditaxel (NAB-PTX) during PIPAC in a Phase I s...
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creator | Ceelen, Wim Sandra, Louis Van de Sande, Leen Graversen, M Mortensen, MB Vermeulen, An Gasthuys, Elke Reynders, Dries Cosyns, Sarah Hoorens, Anne Willaert, Wouter |
description | Background Pressurized intraperitoneal aerosolized chemotherapy (PIPAC) is a novel method to treat patients with peritoneal metastases (PM). We aimed to study the tolerability, safety, pharmacokinetics, and tumour response of nanoparticle albumin bound paditaxel (NAB-PTX) during PIPAC in a Phase I study.
Methods Eligible patients with biopsy-proven PM from ovarian, breast, gastric, hepatobiliary, or pancreatic origin underwent three PIPAC treatments using NAB-PTX with a four-week interval. The dose of NAB-PTX was escalated from 35 to 140 mg/m(2) using a Bayesian design to estimate the maximum tolerated dose (MTD).
Findings Twenty-three patients were induded; thirteen (65%) patients combined PIPAC therapy with continued systemic chemotherapy. The most frequent toxicities were liver toxicity and anaemia. Treatment resulted in seven (35%) responders, six (30%) non-responders and seven (35%) patients with stable PM. Systemic absorption of NAB-PTX was slow, with median peak plasma concentrations reached after 3 to 4 h. Median NAB-PTX tumour tissue concentrations suggested accumulation: 14.6 ng/mg, 19.2 ng/mg and 40.8 ng/mg after the first, second and third PIPAC procedure respectively. EORTC QoL and VAS scores remained stable. Overall survival after one year was 57%.
Interpretation PIPAC with NAB-PTX results in a favourable PK profile and promising anticancer activity in patients with unresectable PM. The MTD and recommended Phase II clinical trial dose are 140 mg/m(2). In patients with impaired hepatobiliary function, a dose of 112.5 mg/m(2) is recommended. Copyright (C) 2022 The Author(s). Published by Elsevier B.V. |
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Methods Eligible patients with biopsy-proven PM from ovarian, breast, gastric, hepatobiliary, or pancreatic origin underwent three PIPAC treatments using NAB-PTX with a four-week interval. The dose of NAB-PTX was escalated from 35 to 140 mg/m(2) using a Bayesian design to estimate the maximum tolerated dose (MTD).
Findings Twenty-three patients were induded; thirteen (65%) patients combined PIPAC therapy with continued systemic chemotherapy. The most frequent toxicities were liver toxicity and anaemia. Treatment resulted in seven (35%) responders, six (30%) non-responders and seven (35%) patients with stable PM. Systemic absorption of NAB-PTX was slow, with median peak plasma concentrations reached after 3 to 4 h. Median NAB-PTX tumour tissue concentrations suggested accumulation: 14.6 ng/mg, 19.2 ng/mg and 40.8 ng/mg after the first, second and third PIPAC procedure respectively. EORTC QoL and VAS scores remained stable. Overall survival after one year was 57%.
Interpretation PIPAC with NAB-PTX results in a favourable PK profile and promising anticancer activity in patients with unresectable PM. The MTD and recommended Phase II clinical trial dose are 140 mg/m(2). In patients with impaired hepatobiliary function, a dose of 112.5 mg/m(2) is recommended. Copyright (C) 2022 The Author(s). Published by Elsevier B.V.</description><identifier>ISSN: 2352-3964</identifier><identifier>EISSN: 2352-3964</identifier><language>eng</language><subject>CARCINOMATOSIS ; GENETIC POLYMORPHISMS ; Medicine and Health Sciences ; METABOLISM ; Nanoparticle ; Paclitaxel ; Peritoneal carcinomatosis ; Peritoneal metastases ; PIPAC</subject><creationdate>2022</creationdate><rights>Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Public License (CC BY-NC-ND 4.0) info:eu-repo/semantics/openAccess</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,315,780,784,4024,27860</link.rule.ids></links><search><creatorcontrib>Ceelen, Wim</creatorcontrib><creatorcontrib>Sandra, Louis</creatorcontrib><creatorcontrib>Van de Sande, Leen</creatorcontrib><creatorcontrib>Graversen, M</creatorcontrib><creatorcontrib>Mortensen, MB</creatorcontrib><creatorcontrib>Vermeulen, An</creatorcontrib><creatorcontrib>Gasthuys, Elke</creatorcontrib><creatorcontrib>Reynders, Dries</creatorcontrib><creatorcontrib>Cosyns, Sarah</creatorcontrib><creatorcontrib>Hoorens, Anne</creatorcontrib><creatorcontrib>Willaert, Wouter</creatorcontrib><title>Phase I study of intraperitoneal aerosolized nanoparticle albumin based paclitaxel (NAB-PTX) for unresectable peritoneal metastases</title><description>Background Pressurized intraperitoneal aerosolized chemotherapy (PIPAC) is a novel method to treat patients with peritoneal metastases (PM). We aimed to study the tolerability, safety, pharmacokinetics, and tumour response of nanoparticle albumin bound paditaxel (NAB-PTX) during PIPAC in a Phase I study.
Methods Eligible patients with biopsy-proven PM from ovarian, breast, gastric, hepatobiliary, or pancreatic origin underwent three PIPAC treatments using NAB-PTX with a four-week interval. The dose of NAB-PTX was escalated from 35 to 140 mg/m(2) using a Bayesian design to estimate the maximum tolerated dose (MTD).
Findings Twenty-three patients were induded; thirteen (65%) patients combined PIPAC therapy with continued systemic chemotherapy. The most frequent toxicities were liver toxicity and anaemia. Treatment resulted in seven (35%) responders, six (30%) non-responders and seven (35%) patients with stable PM. Systemic absorption of NAB-PTX was slow, with median peak plasma concentrations reached after 3 to 4 h. Median NAB-PTX tumour tissue concentrations suggested accumulation: 14.6 ng/mg, 19.2 ng/mg and 40.8 ng/mg after the first, second and third PIPAC procedure respectively. EORTC QoL and VAS scores remained stable. Overall survival after one year was 57%.
Interpretation PIPAC with NAB-PTX results in a favourable PK profile and promising anticancer activity in patients with unresectable PM. The MTD and recommended Phase II clinical trial dose are 140 mg/m(2). In patients with impaired hepatobiliary function, a dose of 112.5 mg/m(2) is recommended. Copyright (C) 2022 The Author(s). Published by Elsevier B.V.</description><subject>CARCINOMATOSIS</subject><subject>GENETIC POLYMORPHISMS</subject><subject>Medicine and Health Sciences</subject><subject>METABOLISM</subject><subject>Nanoparticle</subject><subject>Paclitaxel</subject><subject>Peritoneal carcinomatosis</subject><subject>Peritoneal metastases</subject><subject>PIPAC</subject><issn>2352-3964</issn><issn>2352-3964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ADGLB</sourceid><recordid>eNqdjM1KA0EQhAcxYNC8Qx_1sLDZzZ9HFUUvkkMO3oae2d5sy2Rmme4V9eqLu4KHnAMFVVTx1ZmZVvWyKurb1eL8KF-Ymch7WZbz5WIsN1Pzs-1QCF5AdGi-ILXAUTP2lFlTJAyAlJOkwN_UQMSYeszKPhBgcMOBI7jxoIEefWDFTwpw_Xp3X2x3bzfQpgxDzCTkFd3IHP0eSFFGkVyZSYtBaPbvl6Z6etw9PBf7jqLawC6TR7UJ2WL2HX-QHfZ_kyO7Wa-qeV3WJ0G_ft1g-w</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Ceelen, Wim</creator><creator>Sandra, Louis</creator><creator>Van de Sande, Leen</creator><creator>Graversen, M</creator><creator>Mortensen, MB</creator><creator>Vermeulen, An</creator><creator>Gasthuys, Elke</creator><creator>Reynders, Dries</creator><creator>Cosyns, Sarah</creator><creator>Hoorens, Anne</creator><creator>Willaert, Wouter</creator><scope>ADGLB</scope></search><sort><creationdate>2022</creationdate><title>Phase I study of intraperitoneal aerosolized nanoparticle albumin based paclitaxel (NAB-PTX) for unresectable peritoneal metastases</title><author>Ceelen, Wim ; Sandra, Louis ; Van de Sande, Leen ; Graversen, M ; Mortensen, MB ; Vermeulen, An ; Gasthuys, Elke ; Reynders, Dries ; Cosyns, Sarah ; Hoorens, Anne ; Willaert, Wouter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-ghent_librecat_oai_archive_ugent_be_87621303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>CARCINOMATOSIS</topic><topic>GENETIC POLYMORPHISMS</topic><topic>Medicine and Health Sciences</topic><topic>METABOLISM</topic><topic>Nanoparticle</topic><topic>Paclitaxel</topic><topic>Peritoneal carcinomatosis</topic><topic>Peritoneal metastases</topic><topic>PIPAC</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ceelen, Wim</creatorcontrib><creatorcontrib>Sandra, Louis</creatorcontrib><creatorcontrib>Van de Sande, Leen</creatorcontrib><creatorcontrib>Graversen, M</creatorcontrib><creatorcontrib>Mortensen, MB</creatorcontrib><creatorcontrib>Vermeulen, An</creatorcontrib><creatorcontrib>Gasthuys, Elke</creatorcontrib><creatorcontrib>Reynders, Dries</creatorcontrib><creatorcontrib>Cosyns, Sarah</creatorcontrib><creatorcontrib>Hoorens, Anne</creatorcontrib><creatorcontrib>Willaert, Wouter</creatorcontrib><collection>Ghent University Academic Bibliography</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ceelen, Wim</au><au>Sandra, Louis</au><au>Van de Sande, Leen</au><au>Graversen, M</au><au>Mortensen, MB</au><au>Vermeulen, An</au><au>Gasthuys, Elke</au><au>Reynders, Dries</au><au>Cosyns, Sarah</au><au>Hoorens, Anne</au><au>Willaert, Wouter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phase I study of intraperitoneal aerosolized nanoparticle albumin based paclitaxel (NAB-PTX) for unresectable peritoneal metastases</atitle><date>2022</date><risdate>2022</risdate><issn>2352-3964</issn><eissn>2352-3964</eissn><abstract>Background Pressurized intraperitoneal aerosolized chemotherapy (PIPAC) is a novel method to treat patients with peritoneal metastases (PM). We aimed to study the tolerability, safety, pharmacokinetics, and tumour response of nanoparticle albumin bound paditaxel (NAB-PTX) during PIPAC in a Phase I study.
Methods Eligible patients with biopsy-proven PM from ovarian, breast, gastric, hepatobiliary, or pancreatic origin underwent three PIPAC treatments using NAB-PTX with a four-week interval. The dose of NAB-PTX was escalated from 35 to 140 mg/m(2) using a Bayesian design to estimate the maximum tolerated dose (MTD).
Findings Twenty-three patients were induded; thirteen (65%) patients combined PIPAC therapy with continued systemic chemotherapy. The most frequent toxicities were liver toxicity and anaemia. Treatment resulted in seven (35%) responders, six (30%) non-responders and seven (35%) patients with stable PM. Systemic absorption of NAB-PTX was slow, with median peak plasma concentrations reached after 3 to 4 h. Median NAB-PTX tumour tissue concentrations suggested accumulation: 14.6 ng/mg, 19.2 ng/mg and 40.8 ng/mg after the first, second and third PIPAC procedure respectively. EORTC QoL and VAS scores remained stable. Overall survival after one year was 57%.
Interpretation PIPAC with NAB-PTX results in a favourable PK profile and promising anticancer activity in patients with unresectable PM. The MTD and recommended Phase II clinical trial dose are 140 mg/m(2). In patients with impaired hepatobiliary function, a dose of 112.5 mg/m(2) is recommended. Copyright (C) 2022 The Author(s). Published by Elsevier B.V.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CARCINOMATOSIS GENETIC POLYMORPHISMS Medicine and Health Sciences METABOLISM Nanoparticle Paclitaxel Peritoneal carcinomatosis Peritoneal metastases PIPAC |
title | Phase I study of intraperitoneal aerosolized nanoparticle albumin based paclitaxel (NAB-PTX) for unresectable peritoneal metastases |
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