Triapine With Chemotherapy and Radiation Therapy in Treating Patients With IB2-IVA Cervical or Vaginal Cancer (NCT02595879)
Phase I Dose-Escalation Bioavailability Study of Oral Triapine in Combination With Concurrent Chemoradiation for Locally Advanced Cervical Cancer (LACC) and Vaginal Cancer
๐ฉบ Plain-English Summary (8th-Grade Level)
This phase I trial studies the side effects and best dose of triapine when given with radiation therapy and cisplatin in treating patients with stage IB2-IVA cervical or vaginal cancer. Triapine may stop the growth of cancer cells by blocking an enzyme needed for cell growth. Cisplatin is a drug used in chemotherapy that kills cancer cells by damaging their deoxyribonucleic acid (DNA) and stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells and shrink tumors. Adding triapine to standard treatment with cisplatin and radiation therapy may kill more cancer cells.
Who can join: Review the eligibility criteria below.
Location: University of Alabama at Birmingham Cancer Center โ Birmingham, Alabama
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (17 Sites)
- University of Alabama at Birmingham Cancer Center โ Birmingham, Alabama
- Los Angeles General Medical Center โ Los Angeles, California
- USC / Norris Comprehensive Cancer Center โ Los Angeles, California
- Keck Medical Center of USC Pasadena โ Pasadena, California
- University of Kansas Clinical Research Center โ Fairway, Kansas
- University of Kansas Cancer Center โ Kansas City, Kansas
- University of Kansas Hospital-Indian Creek Campus โ Overland Park, Kansas
- University of Kansas Hospital-Westwood Cancer Center โ Westwood, Kansas
- University of Kentucky/Markey Cancer Center โ Lexington, Kentucky
- University of Michigan Rogel Cancer Center โ Ann Arbor, Michigan
- Wayne State University/Karmanos Cancer Institute โ Detroit, Michigan
- Weisberg Cancer Treatment Center โ Farmington Hills, Michigan
- Rutgers Cancer Institute of New Jersey โ New Brunswick, New Jersey
- University of Oklahoma Health Sciences Center โ Oklahoma City, Oklahoma
- UPMC Hillman Cancer Center โ Pittsburgh, Pennsylvania
- University of Virginia Cancer Center โ Charlottesville, Virginia
- VCU Massey Comprehensive Cancer Center โ Richmond, Virginia
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
Explore by condition: All Advanced Cervical Adenocarcinoma clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.