Standard Medical Therapy
DrugIntravenous doublet chemotherapy FOLFIRI or FOLFIRINOX + targeted systemic therapy (anti-EGFR or anti-VEGF).
Administered every 2 weeks for 12 cycles. Dosage and administration at recommended doses.
NCT Number: NCT06681038
The goal of this clinical trial is to learn if Pressurized intraperitoneal aerosol chemotherapy (PIPAC) significantly improve the progression-free survival (PFS) in patients with advanced peritoneal metastasis from colorectal cancer.
Researchers will compare 2 strategies, systemic treatments (chemotherapy + targeted therapy) corresponding to standard treatment with or without intraperitoneal oxaliplatin (PIPAC) to see if PIPAC improve the progression-free survival.
Participants will:
* receive a standard treatment every 2 weeks for 12 cycles of intravenous FOLFIRI or FOLFIRINOX + targeted systemic therapy (anti-EGFR or anti-VEGF) in the both arms. * receive up to a maximum of 4 PIPAC every 6 weeks with pressurized aerosol containing oxaliplatin in experimental arm. * receive a maintenance treatment until progression or until the onset of severe toxicity after 12 cycles. * be asked to perform a CT scan and carcinoembryonic antigen (CEA) assay every 8 weeks until progression
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Phase 2
Centre François Baclesse, Caen, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Intravenous doublet chemotherapy FOLFIRI or FOLFIRINOX + targeted systemic therapy (anti-EGFR or anti-VEGF).
Administered every 2 weeks for 12 cycles. Dosage and administration at recommended doses.
In addition to standard systemic treatment, patients receive also four PIPAC procedures with pressurized aerosol containing oxaliplatin.
The PIPAC procedure is repeated up to a maximum of 4 times every 6 weeks.
Time frame: From randomisation to 18 months after last patient randomisation
Progression free survival (PFS) is defined as the time (in months) from randomisation until the date of progression or death from any cause.
Time frame: From randomisation to 18 months after last patient randomisation
Overall survival (OS) defined as the time between randomisation and death from any cause
Time frame: At enrollment, week 16 and week 32 after the start of treatment
Quality of life between the two groups evaluated by the score of EORTC QLQ-C30 questionnaire
Time frame: At enrollment, week 16 and week 32 after the start of treatment
Quality of life between the two groups evaluated by the scores of EORTC QLQ-CR29 questionnaire
Time frame: From randomisation to 18 months after last patient randomisation
Peritoneal progression free survival defined as the time between the date of randomisation and the date of peritoneal progression or death from any cause.
Time frame: From randomisation to 18 months after last patient randomisation
Obstruction-free survival is defined as the time between the date of randomisation and the appearance of gastrointestinal obstruction requiring medication with high dose of corticosteroïd (> 1mg/kg) or intervention as nasogastric decompression, intraluminal stenting, surgical bypass, or decompression stomy (gastrostomy or ileo/colostomy) or death.
Time frame: At the end of the 12th course of treatment (week 24)
Peritoneal regression grading score (PRGS) on biopsies performed at surgical exploration in both groups, and systematically during 1st and 2nd PIPAC procedure.
Contact information is provided by the study sponsor or research team.
Emilie DEBEAUPUIS
CONTACT
Frédéric DUMONT, MD
CONTACT
Institut Cancerologie de l'Ouest
Other
Systemic Antitumor Treatment with or Without Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) for Colon Peritoneal Metastases - a Multicentre Phase II Randomized Trial (PIPOX02)
Acronym: PIPOX02
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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