RecruitingPhase 2NCT04779554

Flat Dose vs. Weight-based IP Chemotherapy for CRS/HIPEC

A Randomized Phase 2 Trial of Flat Dose vs. Weight-based Dose of Intra-peritoneal (IP) Chemotherapy for Patients Undergoing Cytoreductive Surgery and Heated Intra-peritoneal Chemotherapy (CRS/HIPEC) for Advanced Gastrointestinal Malignancy


Sponsor

Prakash Pandalai

Enrollment

100 participants

Start Date

Jun 4, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

Peritoneal carcinomatosis from advanced gastro-intestinal malignancy has historically been associated with poor overall survival (≤ 12 months) with few treatment options. Cytoreductive surgery (CRS), which involves removal of all macroscopic tumor nodules, combined with direct administration of heated intra-peritoneal (IP) chemotherapy (HIPEC) to the affected peritoneal surfaces, has been shown to be an effective treatment option that extends overall survival among certain cases of peritoneal carcinomatosis. IP chemotherapy allows delivery of a high dose of cytostatic drug directly onto the peritoneal surfaces at risk for microscopic residual disease while systemic exposure remains limited. Additionally, hyperthermia is known to enhance the cytotoxicity of several agents (including Mitomycin C) and improves the depth of peritoneal penetration. This trial will be a randomized phase 2 comparison of flat dose versus weight-based dose Mitomycin C. The hypothesis of this study is that HIPEC weight-based dosing may result in similarly effective peritoneal Mitomycin C concentrations with less systemic absorption and potential systemic toxicity, compared with the HIPEC flat dosing approach in patients undergoing CRS/HIPEC.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study compares two ways of calculating the dose of chemotherapy given directly into the abdomen during a procedure called HIPEC (heated intraperitoneal chemotherapy) — a treatment for abdominal cancers. One method uses a flat dose (same for everyone) and one adjusts the dose based on body weight. The study aims to find out which approach is safer and more effective. **You may be eligible if...** - You have been diagnosed with a low-grade appendix tumor, pseudomyxoma peritonei, appendiceal cancer, or colorectal cancer that has spread to the lining of the abdomen - You are a candidate for cytoreductive surgery (surgery to remove as much cancer as possible) - Your life expectancy is more than 3 months and your organ function is adequate - Your ECOG performance status is 0–2 **You may NOT be eligible if...** - Your cancer has spread outside the abdomen (e.g., to the lungs, liver beyond treatment, or brain) - You have received chemotherapy or radiation within the past 4 weeks Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGMitomycin C, flat dose 40 mg

Mitomycin C will be delivered as heated intraperitoneal chemotherapy (HIPEC) in two flat doses. Dose 1 will be 30mg at minute 0 and dose 2 will be 10 mg at minute 45.

DRUGMitomycin C, weight-based dose 12.5 mg/m2

Mitomycin C will be delivered as heated intraperitoneal chemotherapy (HIPEC) in two weight-based doses of 9.5 mg/m2 at minute 0 and 3 mg/m2 at minute 45.


Locations(2)

University of Kentucky

Lexington, Kentucky, United States

University of Vermont Medical Center

Burlington, Vermont, United States

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NCT04779554


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