Flat Dose vs. Weight-based IP Chemotherapy for CRS/HIPEC
About this study
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.
- Condition
- Peritoneal Carcinomatosis
- Tested
- Mitomycin C, flat dose 40 mg, Mitomycin C, weight-based dose 12.5 mg/m2
- Sponsor
- Prakash Pandalai
Who can join
- Age
- 18 years and older
- Sex
- All sexes
- Healthy volunteers
- Not accepted
Inclusion 8
- Minimum age: 18 years
- Study condition: Peritoneal Carcinomatosis
- 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
Exclusion 10
- 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
2 sites, 2 recruiting
University of Vermont Medical Center
Burlington, Vermont, United States
University of Kentucky
Lexington, Kentucky, United States
Contact
-
Prakash Pandalai, MD
859-323-8920 Prakash.Pandalai@uky.edu
Potential match only. Final eligibility is determined by the study team.