CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 450 enrolled / 450 target
Drug / intervention
Cisplatin +6 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02466971
NCT02466971Phase 3ActiveUpdate Overdue (3.7/mo)Completion was 41mo ago

A Randomized Phase III Trial of Radiation Therapy and Cisplatin Alone or in Combination With Intravenous Triapine in Women With Newly Diagnosed Bulky Stage IB2, Stage II, IIIB, or IVA Cancer of the Uterine Cervix or Stage II-IVA Vaginal Cancer

National Cancer Institute (NCI)·interventional·Posted Jun 9, 2015·Updated Jun 15, 2026

In Brief

A Phase 3 clinical trial evaluating Brachytherapy, Cisplatin, and 5 other interventions for Advanced Vaginal Adenocarcinoma and 20 related conditions. Active but no longer recruiting, targeting 450 participants across 381 sites in 3 countries.

Signals

Enrollment appears stalled

Detailed Summary

This randomized phase III trial studies radiation therapy and cisplatin with triapine to see how well they work compared to the standard radiation therapy and cisplatin alone in treating patients with newly diagnosed stage IB2, II, or IIIB-IVA cervical cancer or stage II-IVA vaginal cancer. Radiation therapy uses high energy protons to kill tumor cells and shrink tumors. Drugs used in chemotherapy, such as cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Triapine may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It is not yet known whether radiation therapy and cisplatin are more effective with triapine in treating cervical or vaginal cancer.

Study Details

Timeline

Phase 3Active
20162017201820192020202120222023202420252026
First PostedJun 9, 2015
Enrollment StartMay 10, 2016
Primary CompletionJan 26, 2023
Study CompletionJul 14, 2026
TodayJul 2, 2026
Enrollment to primary: 6.7 yearsPosted 11.1 years ago

Arms & Interventions

Arm I (cisplatin, IMRT or RT, brachytherapy)active_comparator

Patients receive cisplatin IV over 90 minutes on days 2, 9, 16, 23, 30, (and day 36 or 37 at the treating physician's discretion). Patients then undergo EBRT (either conventional RT or IMRT) QD 5 days a week for 25 fractions followed by LDR or HDR brachytherapy according to institution's standards. Treatment continues in the absence of disease progression or unacceptable toxicity.

Radiation: BrachytherapyDrug: CisplatinRadiation: External Beam Radiation TherapyRadiation: Intensity-Modulated Radiation TherapyOther: Laboratory Biomarker AnalysisRadiation: Radiation Therapy
Arm II (cisplatin, IMRT or RT, brachytherapy, triapine)experimental

Patients receive cisplatin and undergo EBRT followed by brachytherapy as in Arm I. Patients also receive triapine IV over 2 hours on days 1, 3, 5, 8, 10, 12, 15, 17, 19, 22, 24, 26, 29, 31, and 33. Treatment continues in the absence of disease progression or unacceptable toxicity.

Radiation: BrachytherapyDrug: CisplatinRadiation: Intensity-Modulated Radiation TherapyOther: Laboratory Biomarker AnalysisRadiation: Radiation TherapyDrug: Triapine

Interventions

Brachytherapyradiation

Undergo brachytherapy

Cisplatindrug

Given IV

External Beam Radiation Therapyradiation

Undergo EBRT

Intensity-Modulated Radiation Therapyradiation

Undergo IMRT

Laboratory Biomarker Analysisother

Correlative studies

Radiation Therapyradiation

Undergo conventional RT

Triapinedrug

Given IV