Phase
Condition
Carcinoma
Abdominal Cancer
Digestive System Neoplasms
Treatment
Mitomycin C, weight-based dose 12.5 mg/m2
Mitomycin C, flat dose 40 mg
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients diagnosed with one of the following: low-grade appendiceal mucinousneoplasm, appendiceal cancer with peritoneal carcinomatosis, colorectal cancer withperitoneal 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 consentdocument
Exclusion
Exclusion Criteria:
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 orbiologic composition to Mitomycin C.
Pregnant or breast-feeding women
Uncontrolled ongoing illness
Study Design
Connect with a study center
University of Kentucky
Lexington, Kentucky 40536
United StatesActive - Recruiting
University of Vermont Medical Center
Burlington, Vermont 05401
United StatesActive - Recruiting
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