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Setting Up ctDNA Analysis on Archived Plasma Samples

Recruitingn/aAges 18 Years - anyFemaleFondazione Policlinico Universitario Agostino Gemโ€ฆ
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In plain words

What the trial is, and whether it could suit you

This study (DARE part 1) is a single-center, retrospective, observational feasibility study promoted by the Fondazione Policlinico Universitario Agostino Gemelli IRCCS and co-funded by Fondazione AIRC, aimed at evaluating the clinical utility of circulating tumor DNA (ctDNA) for the assessment of minimal residual disease (MRD) in patients with epithelial ovarian cancer (EOC). In early-stage EOC, the current standard of care consists of complete surgical staging followed by platinum-based adjuvant chemotherapy in high-risk patients; however, the benefit of adjuvant treatment remains controversial in optimally staged cases, as no clear overall survival advantage has been demonstrated. Previous evidence has highlighted the limitations of conventional staging and the need for more accurate biomarkers to identify patients at higher risk of recurrence. ctDNA has emerged as a promising non-inva

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Epithelial ovarian cancer but mucinous histotype * Available matched pre-operative and post-operative (4-7 weeks after surgery) plasma samples * Minimum 4 ml of plasma each timepoint * FIGO 2014 stage I-IV addressed to surgery with curative intent (no gross residual disease after surgery) Exclusion Criteria: * Absence of clinical data * Less than 6 months of follow-up from surgery * Diagnosis of other malignancies in the previous 5 years * Absence of one or both of the prespecified timepoints
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What it tests

  • ctDNA
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Where

1 site
Policlinico Universitario A. Gemelli IRCCS
Roma, Italy
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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