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

Last updated: October 8, 2024
Sponsor: Prakash Pandalai
Overall Status: Active - Recruiting

Phase

2

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

NCT04779554
MCC-20-GI-115
  • Ages > 18
  • All Genders

Study 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 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

Total Participants: 100
Treatment Group(s): 2
Primary Treatment: Mitomycin C, weight-based dose 12.5 mg/m2
Phase: 2
Study Start date:
June 04, 2021
Estimated Completion Date:
February 28, 2026

Connect with a study center

  • University of Kentucky

    Lexington, Kentucky 40536
    United States

    Active - Recruiting

  • University of Vermont Medical Center

    Burlington, Vermont 05401
    United States

    Active - Recruiting

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