Status:
COMPLETED
Phase I Trial HIPEC With Nal-irinotecan
Lead Sponsor:
Stony Brook University
Collaborating Sponsors:
Ipsen
Barbara Ann Karmanos Cancer Institute
Conditions:
Peritoneal Cancer
Pseudomyxoma Peritonei
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
The purpose of this study is to assess the effectiveness and safety of intraperitoneal administration of heated nanoliposomal Irinotecan in cytoreductive surgery (CRS), which is surgery designed to re...
Detailed Description
Cytoreductive surgery and heated intraperitoneal chemotherapy consists of two parts: the first is the surgical removal of all grossly visible deposits of cancer from the abdomen; and the second is app...
Eligibility Criteria
Inclusion
- Patients with pseudomyxoma peritonei or peritoneal carcinomatosis of digestive origin or primary peritoneum: appendiceal mucinous tumor or adenocarcinoma (including goblet cell cancer and signet ring cell cancer), colorectal cancer, gastric cancer, primary peritoneal adenocarcinoma, and mesothelioma; regardless of the number of prior treatment lines. Diagnosis of peritoneal metastasis to be confirmed via either clinical or histopathology assessment.
- Age ≥18 years
- Eastern Cooperative Oncology Group performance status of 0 or 1
- Patients must be candidates for grossly complete cytoreduction surgery with life expectancy greater than 3 months
- Patients must have normal organ and marrow function as defined below:
- absolute neutrophil count \>1,500/microliter (mcL) and white blood cells \> 4000/mm3
- platelets \>75,000/microliters
- total bilirubin \< 3x upper limit normal for institutional limits
- aspartate aminotransferase (AST) / Alanine aminotransferase (ALT) \<2.5x institutional upper limit of normal
- creatinine within normal institutional limits
- Documentation of resectable disease extent by radiographic peritoneal carcinomatosis index (PCI) score or preoperative diagnostic surgery/laparoscopy with preoperative measurements taken within 6 weeks of study entry.
- Women of child-bearing potential and men must agree to use adequate contraception (barrier or hormonal plus barrier method of birth control; abstinence) prior to study entry and for the duration of study participation (at least first 6 months). Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
- Ability to understand and the willingness to sign a written informed consent document.
Exclusion
- Patients with peritoneal disease considered to be unresectable according to preoperative clinical criteria.
- Patients who undergo debulking for palliation with persistence of gross residual disease (complete of cytoreduction score 3, CC=3) will be ineligible for the study.
- Large burden visceral metastases or extra-abdominal metastases.
- Patients who have had radiotherapy within 4 weeks prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier. There is no limit on the number of prior lines of chemotherapy.
- Patients may not be receiving any other investigational agents.
- History of allergic reactions to nal-IRI or irinotecan.
- 7 Uncontrolled ongoing illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
- 8 Pregnant or breast-feeding women are excluded from this study.
- 9 HIV-positive patients on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions. In addition, these patients are at increased risk of lethal infections when treated with marrow-suppressive therapy.
Key Trial Info
Start Date :
October 22 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 14 2022
Estimated Enrollment :
18 Patients enrolled
Trial Details
Trial ID
NCT04088786
Start Date
October 22 2019
End Date
April 14 2022
Last Update
May 6 2022
Active Locations (2)
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1
University of Kentucky
Lexington, Kentucky, United States, 40536
2
Stony Brook University Cancer Center
Stony Brook, New York, United States, 11794