Clinical trial · Interventional
Circulating Tumor DNA for the Early Detection of HPV-positive Pelvic Cancer Relapses (CIRCA-HPV)
Circulating Tumor DNA for the Early Detection of HPV-positive Pelvic Cancer Relapses
NCT03739775CI-TRIAL-00117150CIRCA-HPVcompletedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
ctDNA detection in patients with previously treated, HPV-induced, stage II or III invasive pelvic cancer and who are currently in post-treatment follow-up.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| HPV Positive Pelvic Cancer | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Blood sampling | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- OTHER
- label
- Blood sampling
- interventionNames
- Procedure: Blood sampling
Primary outcomes (2)
- measure
- Sensitivity of plasma circulating tumor DNA detection as a test to detect any (local or distant) relapse in patients who have been curatively treated for HPV-induced invasive pelvic cancer (cervix, anal canal, vagina, vulva, penis).
- timeFrame
- up to 36 months
- description
- Sensitivity= % of patients with number of copies/ml of ctDNA \> threshold among those who experience a relapse within 6 months (+14 days) after the blood draw.
- measure
- Specificity of plasma circulating tumor DNA detection as a test to detect any (local or distant) relapse in patients who have been curatively treated for HPV-induced invasive pelvic cancer (cervix, anal canal, vagina, vulva, penis).
- timeFrame
- up to 36 months
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. 1\) Patient curatively treated within the past 3 years for: * a HPV-induced stage Ib3, Ic, II or III cervix cancer * a HPV-induced stage II or III anal canal, vagina, vulva or penis cancer 2. Patient with no evidence of any invasive tumor at inclusion (clinical and, if any, radiological exams). 3. Age ≥ 18 years 4. Availability of HPV genotyping of the treated cancer and/or archived tumor tissue available. 5. Patient who a follow-up visit is scheduled in the including center at least twice a year. 6. Patient being affiliated to the French social security. 7. Ability to understand and the willingness to sign a written informed consent document. Exclusion Criteria: 1. Patient presenting with active invasive tumor masses (e.g. stage IV cancer). 2. Patient deprived from ability to decide on her own or placed under the authority of a tutor. 3. Patient unable to have a regular follow up for geographical, social or psychological reasons.
References
Publications (0)
Data not yet available
No reference posted for this study.