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

Recruiting now · Phase 2

Conditions studied: Peritoneal Carcinomatosis

In brief

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.

Key facts

Study ID

NCT04779554

Run by

Prakash Pandalai

People needed

100

Starts

2021-06-04

Expected to finish

2028-02-01

Last updated by the study team

2026-04-01

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients diagnosed with one of the following: low-grade appendiceal mucinous neoplasm, pseudomyxoma peritonei, appendiceal cancer with peritoneal carcinomatosis, colorectal cancer with peritoneal carcinomatosis
• ECOG performance status < 3
• Candidate for grossly complete cytoreductive surgery
• Life expectancy greater than 3 months
• Adequate organ and marrow function
• Ability to understand and the willingness to sign a written informed consent document

You may not qualify if…

• Any extra-abdominal metastases
• Untreated lung metastases
• Liver metastases not amenable to resection or ablation
• Known brain metastases
• Chemotherapy or radiotherapy within 4 weeks prior to entering the study
• Presence of residual significant adverse events attributed to prior cancer treatment
• Currently receiving any other investigational therapeutic agents
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to Mitomycin C.
• Pregnant or breast-feeding women
• Uncontrolled ongoing illness

Where it is running

• University of Kentucky — Lexington, Kentucky, United States (enrolling)
• University of Vermont Medical Center — Burlington, Vermont, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.