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NCT Number: NCT06681038

Systemic Antitumor Treatment with or Without Pressurized Intraperitoneal Aerosol Chemotherapy for Colon Peritoneal Metastases (PIPOX02)

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Centre François Baclesse, Caen, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ECOG performance status of 0 to 2;
  • Histopathologically confirmed colonic adenocarcinoma with synchronous or metachronous peritoneal metastasis (PM);
  • Unresectable PM defined as any of the following:
  • PCI >15
  • Extended small bowell involvement
  • Poor general condition contra-indication to a major abdominal surgery (eg: a complete cytoreductive surgery), as decided by the medico-surgical team of the investigator's site specialised in peritoneal carcinomatosis in charge of the patient.
  • A surgical exploration performed less than 4 weeks before inclusion (if not, a laparoscopic exploration must be performed);
  • First line systemic chemotherapy for advanced / metastatic colonic adenocarcinoma. Systemic chemotherapy in an adjuvant setting is allowed if completed more than 6 months before recurrence and without persistent oxaliplatin-induced neuropathy;
  • No extended intraperitoneal adherences defined by at least 9 out of 13 abdominal regions correctly explored during surgical exploration (laparoscopy or laparotomy;

Exclusion criteria

  • Other cancer treated within the last 3 years, with the exception of in situ cervical carcinoma or basocellular carcinoma;
  • Rectal cancer primary (tumor <15 cm from the anal verge);
  • Mutational status corresponding to microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR);
  • Complete or partial bowel obstruction unresponsive to medical treatment;
  • Extraperitoneal polymetastatic diseases. (Only oligometastatic1 diseases are allowed for inclusion);
  • History of abdominal fistula, gastrointestinal perforation, intra-abdominal abscess within 6 months prior to enrolment;
  • Active gastrointestinal bleeding;
  • Inflammatory bowel disease;
  • Peripheral neuropathy according to the Common Toxicity Criteria for Adverse Events (CTCAE) version 5.0, grade ≥2

Treatment and study plan

Standard Medical Therapy

Drug

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.

PIPAC

Procedure

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.

Primary outcomes

  1. Progression free survival (PFS) between the two groups

    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.

Secondary outcomes

  1. Overall survival (OS) between the two groups

    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

  2. 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 score of EORTC QLQ-C30 questionnaire

  3. EORTC QLQ-CR29 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

  4. Peritoneal progression free survival (PPFS) between the two groups

    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.

  5. Obstruction-free survival (OFS) between the two groups

    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.

  6. Histological tumor response

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Emilie DEBEAUPUIS

CONTACT

[email protected]

+33240679844

Frédéric DUMONT, MD

CONTACT

[email protected]

+33240679900

Sponsors and collaborators

Lead sponsor

Institut Cancerologie de l'Ouest

Other

Registry information

Official study title

Systemic Antitumor Treatment with or Without Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) for Colon Peritoneal Metastases - a Multicentre Phase II Randomized Trial (PIPOX02)

Acronym: PIPOX02

Important dates

Study start
2025
Primary completion
2029
Study completion
2029
First posted
Nov 8, 2024
Registry last updated
Nov 8, 2024

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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