Oxaliplatin use in pressurized intraperitoneal aerosol chemotherapy (PIPAC) is safe and effective: A multicenter study
Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is a new drug delivery method used in patients with peritoneal cancer (PC) of primary or secondary origin. Intraperitoneal use of oxaliplatin raises concerns about toxicity, especially abdominal pain. The objective of this study was to assess...
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Veröffentlicht in: | European journal of surgical oncology 2019-12, Vol.45 (12), p.2386-2391 |
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container_title | European journal of surgical oncology |
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creator | Sgarbura, Olivia Hübner, Martin Alyami, Mohammad Eveno, Clarisse Gagnière, Johan Pache, Basile Pocard, Marc Bakrin, Naoual Quénet, François |
description | Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is a new drug delivery method used in patients with peritoneal cancer (PC) of primary or secondary origin. Intraperitoneal use of oxaliplatin raises concerns about toxicity, especially abdominal pain. The objective of this study was to assess the tolerance of PIPAC with oxaliplatin (PIPAC-Ox) in a large cohort of patients and to identify the risk factors for high grade toxicity, discontinuation of treatment and impaired survival.
This retrospective cohort study included all consecutive patients treated with PIPAC-Ox (92 mg/m2) in five centers specialized in the treatment of PC. The procedure was repeated every 6 weeks. Outcomes of interest were Common Terminology Criteria for Adverse Events (CTCAE), symptoms and survival (Kaplan-Meier). Univariate risk factors were included in a multinominal regression model to control for bias.
Overall, 251 PIPAC-Ox treatments were performed in 101 patients (45 female) having unresectable PC of various origins: 66 colorectal, 15 gastric, 5 ovarian, 3 mesothelioma, 2 pseudomyxoma, 10 other malignancies (biliary, pancreatic, endocrine) respectively. The median PCI was 19 (IQR: 10–28). Postoperative abdominal pain was present in 23 patients. Out of the 9 patients with grade 3 abdominal pain, only 3 needed a change of PIPAC drug. CTCAE 4.0 toxicity grade 4 or higher was encountered in 16(15.9%) patients. The patients had a mean of 2.5 procedures/patient (SD = 1.5). 50 subjects presented with symptom improvement.
Oxaliplatin-based PIPAC appears to be a safe treatment that offers good symptom control and promising survival for patients with advanced peritoneal disease. |
doi_str_mv | 10.1016/j.ejso.2019.05.007 |
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This retrospective cohort study included all consecutive patients treated with PIPAC-Ox (92 mg/m2) in five centers specialized in the treatment of PC. The procedure was repeated every 6 weeks. Outcomes of interest were Common Terminology Criteria for Adverse Events (CTCAE), symptoms and survival (Kaplan-Meier). Univariate risk factors were included in a multinominal regression model to control for bias.
Overall, 251 PIPAC-Ox treatments were performed in 101 patients (45 female) having unresectable PC of various origins: 66 colorectal, 15 gastric, 5 ovarian, 3 mesothelioma, 2 pseudomyxoma, 10 other malignancies (biliary, pancreatic, endocrine) respectively. The median PCI was 19 (IQR: 10–28). Postoperative abdominal pain was present in 23 patients. Out of the 9 patients with grade 3 abdominal pain, only 3 needed a change of PIPAC drug. CTCAE 4.0 toxicity grade 4 or higher was encountered in 16(15.9%) patients. The patients had a mean of 2.5 procedures/patient (SD = 1.5). 50 subjects presented with symptom improvement.
Oxaliplatin-based PIPAC appears to be a safe treatment that offers good symptom control and promising survival for patients with advanced peritoneal disease.</description><identifier>ISSN: 0748-7983</identifier><identifier>EISSN: 1532-2157</identifier><identifier>DOI: 10.1016/j.ejso.2019.05.007</identifier><identifier>PMID: 31092362</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Cancer ; Intraperitoneal chemotherapy ; Life Sciences ; Oxaliplatin ; Peritoneal cancer ; PIPAC ; Tolerance</subject><ispartof>European journal of surgical oncology, 2019-12, Vol.45 (12), p.2386-2391</ispartof><rights>2019 Elsevier Ltd, BASO ~ The Association for Cancer Surgery, and the European Society of Surgical Oncology</rights><rights>Copyright © 2019 Elsevier Ltd, BASO ~ The Association for Cancer Surgery, and the European Society of Surgical Oncology. All rights reserved.</rights><rights>Attribution - NonCommercial</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-306625d6431fb161e74ea6a038ed2cdc957f3a05f443758ec992b6df066f4c353</citedby><cites>FETCH-LOGICAL-c434t-306625d6431fb161e74ea6a038ed2cdc957f3a05f443758ec992b6df066f4c353</cites><orcidid>0000-0002-4793-0008 ; 0000-0002-6965-3697</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejso.2019.05.007$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31092362$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.umontpellier.fr/hal-02432145$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Sgarbura, Olivia</creatorcontrib><creatorcontrib>Hübner, Martin</creatorcontrib><creatorcontrib>Alyami, Mohammad</creatorcontrib><creatorcontrib>Eveno, Clarisse</creatorcontrib><creatorcontrib>Gagnière, Johan</creatorcontrib><creatorcontrib>Pache, Basile</creatorcontrib><creatorcontrib>Pocard, Marc</creatorcontrib><creatorcontrib>Bakrin, Naoual</creatorcontrib><creatorcontrib>Quénet, François</creatorcontrib><title>Oxaliplatin use in pressurized intraperitoneal aerosol chemotherapy (PIPAC) is safe and effective: A multicenter study</title><title>European journal of surgical oncology</title><addtitle>Eur J Surg Oncol</addtitle><description>Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is a new drug delivery method used in patients with peritoneal cancer (PC) of primary or secondary origin. Intraperitoneal use of oxaliplatin raises concerns about toxicity, especially abdominal pain. The objective of this study was to assess the tolerance of PIPAC with oxaliplatin (PIPAC-Ox) in a large cohort of patients and to identify the risk factors for high grade toxicity, discontinuation of treatment and impaired survival.
This retrospective cohort study included all consecutive patients treated with PIPAC-Ox (92 mg/m2) in five centers specialized in the treatment of PC. The procedure was repeated every 6 weeks. Outcomes of interest were Common Terminology Criteria for Adverse Events (CTCAE), symptoms and survival (Kaplan-Meier). Univariate risk factors were included in a multinominal regression model to control for bias.
Overall, 251 PIPAC-Ox treatments were performed in 101 patients (45 female) having unresectable PC of various origins: 66 colorectal, 15 gastric, 5 ovarian, 3 mesothelioma, 2 pseudomyxoma, 10 other malignancies (biliary, pancreatic, endocrine) respectively. The median PCI was 19 (IQR: 10–28). Postoperative abdominal pain was present in 23 patients. Out of the 9 patients with grade 3 abdominal pain, only 3 needed a change of PIPAC drug. CTCAE 4.0 toxicity grade 4 or higher was encountered in 16(15.9%) patients. The patients had a mean of 2.5 procedures/patient (SD = 1.5). 50 subjects presented with symptom improvement.
Oxaliplatin-based PIPAC appears to be a safe treatment that offers good symptom control and promising survival for patients with advanced peritoneal disease.</description><subject>Cancer</subject><subject>Intraperitoneal chemotherapy</subject><subject>Life Sciences</subject><subject>Oxaliplatin</subject><subject>Peritoneal cancer</subject><subject>PIPAC</subject><subject>Tolerance</subject><issn>0748-7983</issn><issn>1532-2157</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kc1vEzEQxVcIREPhH-CAfGwPu4y_drOISxQBrRSpPcDZcuyx4mi_sL1Rw1-PVyk9chrNzHvv8H5F8ZFCRYHWn48VHuNYMaBtBbICaF4VKyo5KxmVzetiBY1Yl0275lfFuxiPANDypn1bXHEKLeM1WxWnhyfd-anTyQ9kjkjymALGOAf_B21eU9ATBp_GAXVHNIYxjh0xB-zHdMD8PJObx_vHzfaW-Eiidkj0YAk6hyb5E34hG9LPXfIGh4SBxDTb8_vijdNdxA_P87r49f3bz-1duXv4cb_d7EojuEglh7pm0taCU7enNcVGoK418DVaZqxpZeO4BumE4I1co2lbtq-tyzYnDJf8uri95B50p6bgex3OatRe3W12arkBE5xRIU80a28u2imMv2eMSfU-Guw6PeA4R8UYZ8BqgCWWXaQmtxEDupdsCmpho45qYaMWNgqkymyy6dNz_rzv0b5Y_sHIgq8XAeZGTh6DisbjYND6kLtUdvT_y_8LuvmgFw</recordid><startdate>201912</startdate><enddate>201912</enddate><creator>Sgarbura, Olivia</creator><creator>Hübner, Martin</creator><creator>Alyami, Mohammad</creator><creator>Eveno, Clarisse</creator><creator>Gagnière, Johan</creator><creator>Pache, Basile</creator><creator>Pocard, Marc</creator><creator>Bakrin, Naoual</creator><creator>Quénet, François</creator><general>Elsevier Ltd</general><general>WB Saunders</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-4793-0008</orcidid><orcidid>https://orcid.org/0000-0002-6965-3697</orcidid></search><sort><creationdate>201912</creationdate><title>Oxaliplatin use in pressurized intraperitoneal aerosol chemotherapy (PIPAC) is safe and effective: A multicenter study</title><author>Sgarbura, Olivia ; Hübner, Martin ; Alyami, Mohammad ; Eveno, Clarisse ; Gagnière, Johan ; Pache, Basile ; Pocard, Marc ; Bakrin, Naoual ; Quénet, François</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-306625d6431fb161e74ea6a038ed2cdc957f3a05f443758ec992b6df066f4c353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Cancer</topic><topic>Intraperitoneal chemotherapy</topic><topic>Life Sciences</topic><topic>Oxaliplatin</topic><topic>Peritoneal cancer</topic><topic>PIPAC</topic><topic>Tolerance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sgarbura, Olivia</creatorcontrib><creatorcontrib>Hübner, Martin</creatorcontrib><creatorcontrib>Alyami, Mohammad</creatorcontrib><creatorcontrib>Eveno, Clarisse</creatorcontrib><creatorcontrib>Gagnière, Johan</creatorcontrib><creatorcontrib>Pache, Basile</creatorcontrib><creatorcontrib>Pocard, Marc</creatorcontrib><creatorcontrib>Bakrin, Naoual</creatorcontrib><creatorcontrib>Quénet, François</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>European journal of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sgarbura, Olivia</au><au>Hübner, Martin</au><au>Alyami, Mohammad</au><au>Eveno, Clarisse</au><au>Gagnière, Johan</au><au>Pache, Basile</au><au>Pocard, Marc</au><au>Bakrin, Naoual</au><au>Quénet, François</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oxaliplatin use in pressurized intraperitoneal aerosol chemotherapy (PIPAC) is safe and effective: A multicenter study</atitle><jtitle>European journal of surgical oncology</jtitle><addtitle>Eur J Surg Oncol</addtitle><date>2019-12</date><risdate>2019</risdate><volume>45</volume><issue>12</issue><spage>2386</spage><epage>2391</epage><pages>2386-2391</pages><issn>0748-7983</issn><eissn>1532-2157</eissn><abstract>Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is a new drug delivery method used in patients with peritoneal cancer (PC) of primary or secondary origin. Intraperitoneal use of oxaliplatin raises concerns about toxicity, especially abdominal pain. The objective of this study was to assess the tolerance of PIPAC with oxaliplatin (PIPAC-Ox) in a large cohort of patients and to identify the risk factors for high grade toxicity, discontinuation of treatment and impaired survival.
This retrospective cohort study included all consecutive patients treated with PIPAC-Ox (92 mg/m2) in five centers specialized in the treatment of PC. The procedure was repeated every 6 weeks. Outcomes of interest were Common Terminology Criteria for Adverse Events (CTCAE), symptoms and survival (Kaplan-Meier). Univariate risk factors were included in a multinominal regression model to control for bias.
Overall, 251 PIPAC-Ox treatments were performed in 101 patients (45 female) having unresectable PC of various origins: 66 colorectal, 15 gastric, 5 ovarian, 3 mesothelioma, 2 pseudomyxoma, 10 other malignancies (biliary, pancreatic, endocrine) respectively. The median PCI was 19 (IQR: 10–28). Postoperative abdominal pain was present in 23 patients. Out of the 9 patients with grade 3 abdominal pain, only 3 needed a change of PIPAC drug. CTCAE 4.0 toxicity grade 4 or higher was encountered in 16(15.9%) patients. The patients had a mean of 2.5 procedures/patient (SD = 1.5). 50 subjects presented with symptom improvement.
Oxaliplatin-based PIPAC appears to be a safe treatment that offers good symptom control and promising survival for patients with advanced peritoneal disease.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>31092362</pmid><doi>10.1016/j.ejso.2019.05.007</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-4793-0008</orcidid><orcidid>https://orcid.org/0000-0002-6965-3697</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Cancer Intraperitoneal chemotherapy Life Sciences Oxaliplatin Peritoneal cancer PIPAC Tolerance |
title | Oxaliplatin use in pressurized intraperitoneal aerosol chemotherapy (PIPAC) is safe and effective: A multicenter study |
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