Pasireotide to Reduce Clinically Relevant Digestive Leakage After Complete Cytoreductive Surgery (CRS) Plus Hyperthermic Intra-Peritoneal Chemotherapy (HIPEC) for Peritoneal Carcinomatosis

  • STATUS
    Recruiting
  • End date
    Sep 8, 2023
  • participants needed
    217
  • sponsor
    Gustave Roussy, Cancer Campus, Grand Paris
Updated on 8 April 2021

Summary

To assess the efficacy of pasireotide in the reduction of clinically relevant postoperative digestive leakage after CRS plus HIPEC compared to placebo

Details
Condition Abdominal Neoplasm, Neoplasm of unspecified nature of digestive system, Peritoneal Carcinomatosis, Abdominal Cancer, Digestive System Neoplasms
Treatment Pasireotide 0.9 MG/ML, Saline water
Clinical Study IdentifierNCT04826432
SponsorGustave Roussy, Cancer Campus, Grand Paris
Last Modified on8 April 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Male or female patients aged between 18 years and 75 years included
ECOG (Eastern Cooperative Oncology Group) Performance Status 2
Primary (pseudomyxoma peritonei, peritoneal mesothelioma) or Secondary (colorectal or ovarian) peritoneal malignancies
Curative intent resection obtained by a complete resection according to the Completeness of Cytoreduction score (CC) (CC 0-1) followed by HIPEC Different intraperitoneal drug administration modalities such as neoadjuvant systemic plus simultaneous intraperitoneal and intravenous chemotherapy (NIPS) or pressurized intra-peritoneal aerosol chemotherapy (PIPAC) does not represent exclusion criteria
Absence of extra-peritoneal metastatic disease or limited hepatic or lung metastases easily amenable to curative-intent resection or ablation
Intraoperative Peritoneal Cancer Index (PCI score) 10
Visceral resection with at least one digestive anastomosis with or without loop ileostomy or pancreatic or biliary resection
Negative serum pregnancy test for women of childbearing potential within 7 days prior to therapy
Sexually active women of childbearing potential must agree to use a highly effective method of contraception or to abstain from sexual activity during the study and for 3 months after the last study treatment administration. Sexually active males patients must agree to use condom or to abstain from sexual activity during the study and for 3 months after the last study treatment administration. Also, it is recommended their women of childbearing potential partner use a highly effective method of contraception during the same period
Patient should understand, sign, and date the written informed consent form prior to any protocol-specific procedures performed. Patient should be able and willing to comply with study visits and procedures as per protocol
Patients must be affiliated to a social security system or beneficiary of the same

Exclusion Criteria

Macroscopically incomplete surgical resection (CC 2)
Standard contraindications to pasireotide
patients with uncontrolled diabetes mellitus or a fasting plasma glucose > 250mg/dl (14 mMol/L)
patients who have congestive heart failure (NYHA Class III or IV), unstable angina, sustained ventricular tachycardia, ventricular fibrillation, clinically significant bradycardia including a corrected QT (QTc) interval longer than 450 msec, advanced heart block or a history of acute myocardial infarction within the six months preceding enrollment
patients with liver disease such as severe hepatic impairment (Child Pugh C), chronic active hepatitis or chronic persistent hepatitis with abnormal coagulation (INR>1.5)
patients with the presence of active or suspected acute or chronic uncontrolled infection
hypersensitivity to somatostatin analogues or any component of pasireotide formulations
patients with uncontrolled hypothyroidism
Patients participating or who have participated to another study evaluating the effect of a new drug other than pasireotide within 1 month prior to dosing
Patient who have already participated to this study (a patient can only be included once in the study)
Patients with a history of non-compliance to medical regimens or who are considered potentially unreliable or will be unable to complete the entire study
Women who are pregnant or likely to be so, or who are breastfeeding
Patient under guardianship or deprived of his liberty by a judicial or administrative decision or incapable of giving its consent
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