Gastric Cancer Clinical Trial
— CUREOfficial title:
Clinical Utility of Circulating Tumor DNA in Gastro-Esophageal Cancer
NCT number | NCT04576858 |
Other study ID # | CURE |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | February 3, 2020 |
Est. completion date | July 2025 |
This is a prospective cohort study designed to evaluate the treatment effect as well as
predictive and prognostic factors with special emphasis on the clinical utility of ctDNA in
plasma in patients with gastroesophageal cancer. Patients with gastroesophageal cancer are
included in 5 separate cohorts scheduled for
- Surgical resection + perioperative chemotherapy (cohort 1)
- Neoadjuvant chemoradiotherapy followed by surgical resection (cohort 2)
- Definitive chemoradiotherapy with curative intent (cohort 3)
- Systemic therapy with the intent to prolong survival (cohort 4)
- Palliative treatment without the use of chemotherapy (cohort 5)
Status | Recruiting |
Enrollment | 1950 |
Est. completion date | July 2025 |
Est. primary completion date | February 2025 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: Gastroesophageal cancer Age 18 years or older Able to understand and sign written informed consent Exclusion Criteria: Patients not providing informed consent |
Country | Name | City | State |
---|---|---|---|
Denmark | Rigshospitalet | Copenhagen |
Lead Sponsor | Collaborator |
---|---|
Rigshospitalet, Denmark |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time to recurrence | 1 year | ||
Secondary | Time to progression | 1 year | ||
Secondary | Overall survival | 5 year | ||
Secondary | Response rate RECIST 1.1 | through study completion, an average of 1 year | ||
Secondary | Response duration RECIST 1.1 | through study completion, an average of 1 year |
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