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Validation of a miRNA Panel to Optimize Treatment Response in Patients With Metastatic Pancreatic Cancer (mirPANC 2)

Validation of a miRNA Panel to Optimize Treatment Response in Patients With Metastatic Pancreatic Cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06945978
Acronym
mirPANC 2
Enrollment
60
Registered
2025-04-27
Start date
2025-01-21
Completion date
2027-12-31
Last updated
2025-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epigenetic, Metastasis, Pancreatic Cancer

Keywords

Pancreatic cancer, miRNA, Treatment response, Epigenetic, Folfirinox

Brief summary

This study is being conducted to better understand how pancreatic cancer behaves during treatment and how we can improve methods for monitoring disease progression. The research aims to determine whether small molecules present in the blood, called miRNAs, can help doctors assess whether the treatment is working or needs adjustment. With this, we hope to make cancer monitoring less invasive and more precise, allowing patients to receive more personalized and effective treatments.

Detailed description

Pancreatic cancer, particularly Pancreatic Ductal Adenocarcinoma (PDAC), has an extremely poor prognosis, with a 5-year survival rate of less than 3% for advanced stages. In 2020, Brazil saw about 11,893 deaths from this condition, with incidence rates expected to rise. The standard treatment for metastatic PDAC is the FOLFIRINOX regimen, but its response is variable and its effectiveness is limited, with few advancements in personalized therapy and response prediction. This research aims to develop and validate a panel of serum-based miRNA biomarkers using qPCR and large-scale sequencing (NGS) to evaluate treatment response in metastatic PDAC patients. The goal is to identify miRNA expression patterns that predict the effectiveness of FOLFIRINOX and assist in personalizing treatment based on individual responses. The study will use liquid biopsy to collect blood samples and analyze circulating miRNAs, enabling early detection of treatment responses and disease progression. This will allow for precise therapeutic adjustments and alternative treatment options based on the patient's profile. The innovative approach combines liquid biopsy with miRNA analysis as a low-cost, effective tool for monitoring and personalizing treatment. Using qPCR, a more affordable method than NGS and microarrays, enhances clinical feasibility. The research is highly relevant to the Brazilian Unified Health System (SUS), as an accessible miRNA panel could optimize resource use, reduce costs of ineffective treatments, and improve care quality and outcomes, aligning with SUS's goals for precise and accessible healthcare.

Interventions

None listed

Sponsors

Benedito Mauro Rossi
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with metastatic PDAC; * Patients who will start treatment with FOLFIRINOX; * 18 years or older; * Who agree to participate in the study by signing the Informed Consent Form;

Exclusion criteria

* Patients who have previously undergone chemotherapy, whether neoadjuvant, adjuvant, or any prior first-line treatment; * Patients who do not meet the minimum criteria to receive the proposed regimen, such as those with hyperbilirubinemia, those who are not candidates due to age or performance status deterioration;

Design outcomes

Primary

MeasureTime frameDescription
Response to treatmentAfter 4 cycle of therapy (each cycle is 15 days)Response to FOLFIRINOX treatment after 4 cycles of therapy.

Countries

Brazil

Contacts

Primary ContactCamila Farias
camila.farias@bp.org.br+551135054680
Backup ContactBianca Verboski
bianca.verboski@bp.org.br+551135052639

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026