2022-502117-29-00RecruitingPhase 3
Short or long NAT for BR/LAPC (ADVANTAGE Trial)
Standard versus Prolonged Neoadjuvant (Conversion) Chemotherapy to prolong survival of patients with Borderline and Locally Advanced Pancreatic Cancer: a phase III randomized controlled trial
Source: EU CTIS (euclinicaltrials.eu) · Last updated 22 Jun 2026
Brief summary (registry, in English)
To assess the optimal duration of preoperative chemotherapy before conversion surgery for patients with borderline and locally advanced pancreatic ductal adenocarcinoma in attempt to improve survival
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 754 (estimated)
- First submitted
- 10 Nov 2022
- Start date
- 19 Oct 2023
- Lead sponsor
- Vastra Gotalandsregionen
- Diseases
- Pancreatic cancer
- EU CT number
- 2022-502117-29-00
What you commit to
- Study type: Interventional · Phase 3
- Planned participants: 754
- 5 sites in 2 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.
Who cannot take part
Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.
Lab values
- Co-morbidity precluding pancreatic surgery or chemotherapy - Sensitivity to any of the drugs in the proposed management regimens - ECOG ≥2 - neuropathy ≥ grade 2 according to Common Terminology Criteria for Adverse Events (CTCAE), version 6 [47] - granulocyte count < 1500 per cubic millimetre (< 1,5 x 109/L) - platelet count < 100 000 per cubic millimetre (< 100 x 109/L) - serum creatinine > 1.5 UNL (upper limit normal range) - albumin <2,5 g/dl (<25 g/L) - total bilirubin >3 x ULN - ASAT (SGOT) and ALAT (SGPT) >2.5 x institutional ULN - female patients in child-bearing age not using adequate contraception, pregnant or lactating women - mental or somatic disorders which could possibly interfere with informed consent, compliance or the planned treatments - previous oncologic treatment for pancreatic adenocarcinoma within the past 5 years - Any reason according to the investigator why the patient cannot comply with the protocol or is not suitable to participate
Who the study is looking for
- Borderline or locally advanced pancreatic adenocarcinoma at diagnosis according to NCCN Clinical Practice Guidelines, version 1.2022 • Histo- or cytologically confirmed adenocarcinoma • T1-4, Nx, M0 according to AJCC 8th edition • Age ≥ 18 years-of-age • ECOG 0-1 and considered fit for the planned chemotherapy and surgery • Written informed patient consent
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (5)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Krankenhaus Nordwest GmbH | Frankfurt am Main | Germany | Not yet recruiting |
| University Medical Center Hamburg-Eppendorf | Hamburg | Germany | Not yet recruiting |
| Universitaetsklinikum Heidelberg AöR | Heidelberg | Germany | Not yet recruiting |
| Sahlgrenska University Hospital-Vastra Gotalandsregionen | Goteborg | Sweden | Recruiting |
| Karolinska University Hospital | Huddinge | Sweden | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.