ClinicalTrials.gg
RecruitingNCT07144917ImPaHLAUpdated Mar 30, 2026

Immunoparalysis After Pancreaticoduodenectomy

An observational study in Pancreatic Ductal Adenocarcinoma (mPDAC), Pancreatic Head Tumour and Pancreatic Fistula, sponsored by Hospices Civils de Lyon. Recruiting at 4 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-30.

Sponsored by Hospices Civils de Lyon · Observational

From the registry’s dates

  • Started Mar 2026; still recruiting 7 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study 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

02

Conditions studied

  • Pancreatic Ductal Adenocarcinoma (mPDAC)
  • Pancreatic Head Tumour
  • Pancreatic Fistula

Keywords

  • Pancreaticoduocenectomy
  • Pancreatic fistula
  • Post-Operative Pancreatic Fistula
  • Post-Pancreatectomy Acute Pancreatitis
  • Pancreatic complications
  • Sepsis
  • mHLA-DR
  • Immunparalysis
  • Immunosuppression
03

In context

Pancreatic Fistula

122 studies on the registry are indexed under Pancreatic Fistula; 27 are open to participants now.

This study's planned enrollment of 100 is below the median of 120 across 44 observational studies indexed under Pancreatic Fistula.

Browse Pancreatic Fistula studies →

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,866 studies on the registry; 448 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

100 patients undergoing a Pancreaticoduodenectomy in one of the four participating centers for a benign or malignant tumor of the pancreatic head will be included.

Participating centers : Hospices Civils de Lyon (Edouard Herriot Hospital, Croix-Rousse Hospital, Lyon Sud Hospital) and Centre Léon Bérard, Lyon, France

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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
  • 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 (and CD4 \< cells/mm³)
    • Aplasia defined by circulating \< 500 cells/mm³
    • Immunosuppressive treatment other than chemotherapy : Biotherapy, 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
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Absolute neutrophil count (ANC)

The number of neutrophils, white blood cells that help fight infection, in a given amount of blood. Too few raises the risk of infection.

It is a count, not a percentage of the white cells. Limits are written in units that mean the same: ≥ 1.5 × 10⁹/L is ≥ 1,500 per mm³ (µL). Each lab has its own reference range.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Adults patients undergoing Pancreaticoduodenectomy in one for a benign or malignant tumor of the pan

    Biological : blood sample mHLA-DR analysis will be realized on Cyto-Chex® BCT anticoagulant tubes (5mL). Each sample will be transported and centralized at the Immunology Laboratory of Edouard Herriot Hospital and analyzed by flow cytometry. Results will be expressed as number of receptors per monocyte (Ab/C) Samples will be collected : * The day of surgery before intervention * The day of surgery after intervention * At postoperative day one * At postoperative day two * At postoperative day three * At postoperative day four * At postoperative day five * At postoperative day seven

    Diagnostic Test: mHLA-DR analysis

Interventions

  • Diagnostic testmHLA-DR analysis

    mHLA-DR analysis will be realized on Cyto-Chex® BCT anticoagulant tubes (5mL). Each sample will be transported and centralized at the Immunology Laboratory of Edouard Herriot Hospital and analyzed by flow cytometry. Samples will be collected : * The day of surgery before intervention * The day of surgery after intervention * At postoperative day one * At postoperative day two * At postoperative day three * At postoperative day four * At postoperative day five * At postoperative day seven

06

What researchers measure

Primary outcomes

  1. mHLA-DR expressed by numbers of antibody per cells (Ab/C)

    Association of expression of mHLA-DR at POD1, POD 2 and POD3 and occurrence of pancreatic complications (CR-POPF, CR-PPAP, PACE criteria) PACE (PAncreatic Composite Endpoint) is a binary composite endpoint including : CR-POPF or Hemmorage or Reintervention (endoscopic, radiological, surgical)

    Time frame: mHLA-DR will be assessed during 7 first days - The day of surgery right before intervention (Pre-Op) - The day of surgery immediately after intervention (Post-Op) - At postoperative day one (POD1) - At postoperative day two (POD2) - At postoperative day

07

Study locations

1 of 4 sites recruiting
  • Julie PERINEL
    Lyon, 69003, France
    Not yet recruiting
  • Xavier MULLER
    Lyon, 69004, France
    Recruiting
  • Aurélien DUPRE
    Lyon, 69008, France
    Not yet recruiting
  • Jean-Christophe LIFANTE
    Pierre-Bénite, 69495, France
    Not yet recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 30, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07144917
Responsible party
Sponsor
First posted
Aug 28, 2025
Start date
Mar 18, 2026
Primary completion
Mar 18, 2027 (estimated)
Completion
Jun 18, 2027 (estimated)
Last update
Mar 30, 2026

Study contacts

OU Rithya
Contact
rithya.ou@chu-lyon.fr
06 09 32 60 60
Dr Xavier MULLER
Contact
xavier.muller@chu-lyon.fr
04 72 11 80 88

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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