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

Inclusion Criteria6

  • 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 Criteria10

  • 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

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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