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Clinical Trials in France / NCT04575363
Recruiting Not applicable

RPSA as a Potential Prognostic Biomarker of Pancreatic Cancer

NCT04575363 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2021-10-18
Last updated
2023-11-09

Condition(s) studied

Pancreatic Ductal Adenocarcinoma (PDAC)

Investigational drug(s) / intervention(s)

Blood sample

Blood sample: Blood sample

Study summary

PDAC (Pancreatic ductal adenocarcinoma) represents 90% of pancreatic tumors. The prognosis of PDAC remains poor at this time. Its management is based on surgery for early stages, associated with neoadjuvant and adjuvant chemotherapy. However, around 80% of patients will relapse after surgery. There is a lack of efficient biological biomarkers of PDAC, especially for prognosis. To date, CA19-9 is commonly used despite its lack of sensitivity and specificity.

Ribosomal protein SA (RPSA) is a transmembrane receptor localized at the cell surface but also in the cytosolic and nuclear regions. RPSA interacts with many proteins in the extracellular matrix (ECM), including laminin-1 and elastin. RPSA in involved in different cellular functions such as cell adhesion, migration, proliferation and differentiation. The expression of RPSA is increased in many cancers including breast, lung, prostate, pancreatic, etc. It could represent a molecular biomarker of tumor invasion and metastatic abilities. Moreover, the concentration of RPSA could be measured in the serum of patients with PDAC. Recent data suggest that a modification of the RPSA concentration could be a prognostic biomarker of PDAC.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
inclusion criteria : * Patients treated at the Reims University Hospital for a resectable or potentially resectable pancreatic tumor, with or without neoadjuvant chemotherapy * Adults (aged more than 18 years old) * Patients who have signed the informed consent form exclusion criteria : * Patients with a prior history of cancer (excluding basal cell carcinoma or in situ cervical cancer that received conventional cancer treatment). * Minors * Patients for whom PDAC is not the retained diagnosis

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Damien JOLLY Reims France Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04575363 on ClinicalTrials.gov ↗ ← All trials in France