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Recruiting NCT07144917

NCT07144917 Immunoparalysis After Pancreaticoduodenectomy

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Clinical Trial Summary
NCT ID NCT07144917
Status Recruiting
Phase
Sponsor Hospices Civils de Lyon
Condition Pancreatic Ductal Adenocarcinoma (mPDAC)
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2026-03-18
Primary Completion 2027-03-18

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
mHLA-DR analysis

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2026-03-18 with a primary completion date of 2027-03-18.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

By 2030, pancreatic adenocarcinoma could become the second leading cause of cancer-related death in France. To date, Pancreaticoduodenectomy (PD) is the standard treatment for resectable adenocarcinoma of the pancreatic head. Despite advances in perioperative care, morbidity remains high, and the occurrence of postoperative complications can negatively impact patient's oncologic prognosis. Sepsis is the leading cause of postoperative death following PD and it remains mainly associated with the development of a clinically-relevant postoperative pancreatic fistula (CR-POPF). More recently, post-pancreatectomy acute pancreatitis (PPAP) has been defined as a very early complication after pancreatic resection. PPAP is an ischemic and inflammatory condition of the pancreatic remnant that may be responsible for nearly half of CR-POPFs. CR-PPAP can lead to sepsis with multiorgan failure and necrotizing pancreatitis, which are with CR-POPF the two main indications for reoperation and completion pancreatectomy. Despite the major impact of severe pancreatic complications on mortality after PD, no reliable early biomarker currently exists to predict their occurence. Immunoparalysis refers to the functional impairment of immune cells with monocytes showing altered capacity of cell presentation. In classical models of inflammation such as acute pancreatitis, sepsis and surgery, the initial systemic inflammatory response syndrome is simultaneously accompanied by a compensatory anti-inflammatory reaction, which may lead to immunoparalysis. mHLA-DR (Human Leukocyte Antigen-DR on Monocytes) is considered as the most appropriate biomarker to assess this immune dysfonction. Various studies emphasize the predictive value of mHLA-DR for early detection of adverse outcomes : in acute pancreatitis, mHLA-DR predicts the onset of severe forms as early as admission and after colorectal surgery, mHLA-DR enables earlier detection of anastomotic leakage compared to conventional biomarkers. The main hypothesis is that the severity of postoperative complications is driven by immunological factors. On one hand, this study seeks to improve the understanding of the relationship between the immune response after PD and the occurrence of pancreatic complications. On the other hand, it aims to assess if mHLA-DR could represent an early biomarker for detecting severe pancreatic complications. Therefore, the main objective of this study is to evaluate the association of mHLA-DR expression in the early postoperative period following PD and the occurrence of severe pancreatic complications

Eligibility Criteria

Inclusion Criteria: * Any patient undergoing a Pancreaticoduodenectomy in one of the four participating centers for a benign or malignant tumor of the pancreatic head Exclusion Criteria: * Age \< 18 years * Pregnant, postpartum, or breastfeeding women * Indication other than tumor-related (e.g., chronic pancreatitis) * Patient with an infectious syndrome at the time of inclusion * Preoperative immunosuppression * Immunosuppressive disease other than cancer: * Congenital or acquired immune deficiency * Functional hyposplenism or asplenia, patient under long-term antibiotic prophylaxis for this reason * Patient with HIV (and CD4 \< cells/mm³) * Aplasia defined by circulating neutrophil count \< 500 cells/mm³ * Immunosuppressive treatment other than chemotherapy : Biotherapy, Corticosteroid therapy \>10 mg/day or cumulative dose \>700 mg prednisolone equivalent : Patient expected to receive immunosuppressive treatment within the first 7 postoperative days * Individuals deprived of liberty by judicial or administrative decisio * Adults under legal protection (guardianship or curatorship) * Individuals not affiliated with a social security scheme or an equivalent coverage * Refusal to participate in the study

Contact & Investigator

Central Contact

OU Rithya

✉ rithya.ou@chu-lyon.fr

📞 06 09 32 60 60

Frequently Asked Questions

Who can join the NCT07144917 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Pancreatic Ductal Adenocarcinoma (mPDAC). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07144917 currently recruiting?

Yes, NCT07144917 is actively recruiting participants. Contact the research team at rithya.ou@chu-lyon.fr for enrollment information.

Where is the NCT07144917 trial being conducted?

This trial is being conducted at Lyon, France, Lyon, France, Lyon, France, Pierre-Bénite, France.

Who is sponsoring the NCT07144917 clinical trial?

NCT07144917 is sponsored by Hospices Civils de Lyon. The trial plans to enroll 100 participants.

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